Beruflich Dokumente
Kultur Dokumente
December 2009
INDEX
S. Name of Equipment Recommended Unit P.No.
No. For
1 BEDS N ACCESSORIES
1. Semi Fowler Bed Deluxe With Castors and Saline 1
Rod
2. I.C.U. BED (Height Adjustable with S.S. 2
Collapsible Railing)
3. Bedside Locker With Drawer and cabinet 3
4. Over bed table (Height Adjustable) 4
5. Examination Couch 4
6. Stretcher on Trolley 5
7. Soiled Linion Trolley (Stainless steel) 5
8. Doctors Examination Stool (Stainless Steel) 6
9. Double Step Stool 6
10. Single Step Stool 7
11. Emergency Recovery Trolley (Causality Trolley) 7
12. Saline Stand – Full S.S. with castor 8
13. Mosquito Rod full S.S. 8
14. Revolving Stool (Stainless Steel) with Backrest 9
15. Patient Attendant bed 9
16. Wheel Chair 9
17. Major Head end controlled hydraulic pump 10
surgical operation theatre super deluxe fully S.S.
model operation table.
18. Minor Hydraulic operation table orthopedic surgery 10
deluxe model
19. Steel cupboard trowel plain 11
20. Slotted Racks 11
21. Equipment Specifications for I.C.U Beds 11
Mechanical-(Non Electrical Model)
22. Table/Trolley 15-23
Sorting Table/ Table Utility with SS Top
Clean up Counter (Wash Station) with
double sink, one middle platform and flash
back
Clean up counter (wash station) with one
sink, one platform and flash back
work table/table utility with SS top
Table trolley with one under shelf
Gauze cutting machine
Line fold table
Preparation and packing table with 2
overhead shelves and 1 drawer
Closed transport trolley with 2 door
shutters and 3 compartments
Instrument trays- perforated type with
handle
Patient Transfer trolley
Semi flower Bed Deluxe with castors and
saline rod
Bed side locker
Stand
over bed table (Height adjustable)
Wheel chair
2
Revolving stool (stainless steel) with
backrest
Medicine trolley
Instrument Trolley
Singh Step Stool
2. CSSD
1. Equipment Specifications for Washer 24
Disinfectors (Medium Capacity)
2. Equipment Specifications for Washer 27
disinfectors (High capacity)
3. Automatic Steam Sterilizer 30
4. Flash Sterilizer 31
5. ETO Sterilizer 32
6. Ultra Sonic Cleaner 33
7. Drying Cabinet 35
8. Sealing Machine : Plain Sealer 35
9. Horizontal high pressure steam sterilizer 36
20"X48" machine
3. ENDO N LAPRO
1. Video Thoracoscope 37
2. Holmium laser generator 39
3. Ultrasonic aspirator 41
4. Specifications for High definition laparoscopy 44
system high definition three chip camera system
5. Equipment Specifications for video enter scope 46
(Single balloon)
6. Equipment Specifications for Video Enter scope 48
(Double balloon)
7. Equipment specifications for video endoscopy 51
complete system
8. Equipment specifications for upper GI endoscope 54
9. Equipment specification for ERCP Scope 56
4. ICU
1. Electric suction Machine Lipo fully stainless steel 59
body
2. Spo2 machine with NIBP (Pulse oxy meter) 59
3. Anesthesia Kit 60
4. syringe infusion pump 60
5. volumetric infusion pump (with Micro and Macro 61
mode of operation)
6. Electric cautery machine 400m 61
7. Central Monitoring System 61
8. Defibrillator with monitoring system 62
9. Electric drilling machine with attachments with 62
reamers flexible
10. Color Multi para monitor 62
11. Ultrasonic Cutting & Coagulation Device 63
12. Cardiopulmonary exercise physiology Test system 66
with Treadmill
13. Stress Test System with TMT 70
14. Sleep Screening Test 72
15. Sleep Lab (Advanced) 74
16. Lung Function Test system 76
17. Lung functions Test system (Advanced) 78
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18. Multipara Monitor 82
19. Defibrillator (Bi-Phasic) 83
8. OPTHOLMALOGY N ENT
1. Slit Lamp Biomicroscope 128
2. Photoslit Lamp 128
3. Direct Ophthal Moscope 129
4. Indirect Ophthalmoscope 130
5. Auto Refractometer 130
6. Tonometer-Non contact 131
7. Applanation Tonometer 131
8. Keratometer 131
9. Motorized Table 131
10. A scan 132
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11. B scan 132
12. Fundus Camera 132
13. Yag Laser 134
14. Humphrey visual field analyser 134
15. Diode laser with LIO facility & slit lamp delivery 135
systerm
16. CRYO unit 135
17. Synaptophore 135
18. Streak retinoscope 136
19. Snellen's Drum 136
20. Ophthalmic refraction unit 137
21. Ocular Thorpe four mirror gonio 138
22. Ocular Thorpe surgical gonioscope 138
23. Kokppe gonio lens set 138
24. Latina SLT gonio lens 138
25. Ocular abraham iridotomy lens 139
26. Ocular swan-jacob autoclaable conoprism 139
27. Goldman perimeter 139
28. Ultrasonic pachymeter 139
29. Phacoemulsifier 140
30. Ophthalmic operating microscope 140
31. Operating microscope with video recording 141
32. wet field bipolar coagulator 141
33. Lennsometer 142
34. surgeon's Chair (Motorized) 142
35. Charts and Cards 142-
1. Teller acuity cards 148
2. Contrast sensitivity Charts
3. Etdrs Charts
4. Ishihara Chat
5. IOL Kit
6. Trial lens set
7. Surgical instruments
9. ENT
1. ENT Head light (for Optimum and Mobile 149
illumination of Medical Examination in ENT)
2. Specifications for Cystoscope Set 149
3. Specifications for stone punch set 149
4. Specifications for Resectoscope set 149
5. Technical specification for Pure Tone Audiometer 150
6. Impedence Audiometer 150
7. Auto Refractometer 150
8. Auto Lensometer with printer 151
9. Keratometer with joystick model 152
10. Ophthalmic chair unit with auto chart projector 152
11. Cateract Set 154
12. Combi video attachment for Tagaki OM 10 Zoom 154
Microscope
13. Specification for high speed electric Drill system 155
10. OT
1. Technical Specifications for Modular OT 157
2. Detailed Technical Specification for Modular 158-
Operation theatre 161
Qalls & Ceiling Construction
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Ceiling Filtration system (Imported)
Door and frames (Hermetically sealed doors)
Operation theatre control panel
Distribution Board
X-Ray viewing Screens
Pressure relief dampers
Operation Theatre Flooring (antistatic
conductive tiles)
Storage Unit
Operating list board
Hatch box
Scrub Station
View Window
3. Operation Table Hydraulic 162
4. Operation Theatre Light 163
5. OT Light with LED Technology Surgical light 165
system based on LED technology
6. Operating Microscope 166
7. OT Table 168
8. OT Light 168
9. Boyle's Apparatus 170
10. Operation Theater light Halogen (Seven Bulb) 171
11. Operation Theater Light Halogen Twin (Seven 171
Bulb+ Four Bulb)
12. Universal Halogen Spot Light 172
11. PAEDTRACIS
1. Infant Incubator Servo Control 173
2. Neonatal Intensive care incubator 175
3. Transport Incubator with Ventilator 177
4. Ventilators Neonatal 179
5. Open care system for neonates 182
6. Neonatal phototherapy unit- CFL 184
7. Neonatal Phototherapy Unit –tube lights 186
8. Fibre optic phototherapy lamp 188
9. Double surface phototherapy unit – tube lights 189
10. Equipment specifications for electronic weighing 191
balance for newborns
11. Paediatric laproscope set with accessories 192
12. Video endoscope system upper GI pediatric 195
Surgery
13. Pediatric Surgery OT Table 198
14. Ultrasonic aspirator for pediatric surgery 200
15. Pediatric Systoscope/ Resectoscope 8-10F 202
16. paediatric bronchoscope 204
17. paedratric oesophagoscope 206
18. warming devices –adult and peadiatric 207
19. neonatal resusitation cart 207
20. neonatal resuscitation unit 208
12. RADIOLOGY
1. IITV System 211
2. usg machine 212
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3. colour doppler 214
4. 500mA X-ray Machine 218
5. 300mA X-ray Machine 219
6. 100mA X-ray Machine 220
7. 60mA X-ray Machine 221
13. VENTILLATOR
1. Ventilator-High End (ICU) 223
2. Transport Monitor 225
3. Anesthesia Machine Trolley 227
4. Ventilator Technical Specification Adult – 228
Paediatric Infatn ventilators
5. Anaesthesia Ventilator 230
6. Transport Ventilator 230
7. Portable ICU Ventilator ICU 231
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EQUIPMENT BEDS N ACCESSORIES- 1
1. SEMI FOWLER BED DELUXE WITH CASTORS AND SALINE ROD
Construction: -
6. Stainless steel bows of 31.75 mm diameter pipe and equal height of 280
mm fixed with colored metal panel on both sides with embossing.
7. Fix panel should be made up of 18G CRCA sheet double press bend on
four sides and uniformly embossed holes from 25mm to 15mm dia and
embossing depth of 4mm in four rows distance between holes should be
125mm.
10. Off set Leg’s should be made up of 31.75 mm diameter and 535 mm long
pipe welded to 37 mm X 37 mm X 3 mm thick X 150 mm long angle, outer
side of angle should have 25 mm X 45deg chamfer.
11. 125 mm Dia heavy-duty castors should be provided two with brakes.
12. Four-flush I.V. Rod locations with S.S. Saline Rod of 12 mm & arrangement
to hold mosquito curtain poles.
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Finish:
13. All components should be pretreated in separate eight-tank process for
better finish, good adhesion and corrosion protection.
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horizontal telescopic type tubes housed in 25.4 mm x 25.4 mm x 18G CRCA square tube.
Arrangement to hold mosquito curtain poles.
Finish: All components should be pretreated in separate eight-tank process for better
finish, good adhesion and corrosion protection. Process includes Hot Degreasing,
Derusting, Activation, Phosphating & No’s of Water rinses as per IS 3618 - 1966 class ‘C’
type and thenpretreated materials is coated with epoxy powder with film thickness of
60 microns (approx.) and then oven baked at 180 degree centigrade.
Construction: - Main cabinet should be made of 1 mm thick “C” shaped one-piece box.
Cabinet should have one drawer at top & a box at bottom and open space in between
drawer & box. Door should be made up of 1.2 mm thick CRCA sheet pivoted at top &
bottom by 4 mm diameter pin. Door & drawer should have magnetic latch of 75mm long
chrome plated brass handle .Top of cabinet should be made up of Stainless steel sheet
304 grades and thickness 24 G. Three sides of the top are raised by 10mm; front side
bend downward and four sides of both tops are bend & pressed 1800 to avoid sharp
edges, supported by 15 mm ply. The main cabinet should be fitted with 50 mm diameter
4 No’s Ball Casters.
Finish: All components should be pretreated in separate eight-tank process for better
finish, good adhesion and corrosion protection. Process includes Hot Degreasing,
Derusting, Activation, Phosphating & No’s of Water rinses as per IS 3618 - 1966 class ‘C’
type and then pretreated materials is coated with epoxy powder with film thickness of
60 microns(approx.) and then oven baked at 180 degree centigrade.
Overall Apron. Size: Stainless Steel Top 760 mm L x 360 mm W 50mm x 25mm MS
tubular telescopic stem with geared S.S. Handle for height adjustment from 75 mm to
1050 mm. MS rectangular tubular base is mounted on four castors of 50 mm dia.
Finish: All components should be pretreated in separate eight-tank process for better
finish, good adhesion and corrosion protection. Process includes Hot Degreasing,
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Derusting, Activation, Phosphating & No’s of Water rinses as per IS 3618 - 1966 class ‘C’
type and then pretreated materials is coated with epoxy powder with film thickness of
60 microns (approx.) and then oven baked at 180 degree centigrade.
5. Examination Couch.
Overall Size: 1830 mm L x 575 mm W x850 mm H (Approx.)
6. Stretcher On Trolley: -
Overall Dimension: - 2035 mm L X 530mm W X 870 mm H (Approx.)
Finish: All components should be pretreated in separate eight-tank process for better
finish, good adhesion and corrosion protection. Process includes Hot Degreasing,
Derusting, Activation, Phosphating & No’s of Water rinses as per IS 3618 - 1966 class ‘C’
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type and then pretreated materials is coated with epoxy powder with film thickness of
60 microns s(approx.) and then oven baked at 180 degree centigrade.
Linton Bag size: 510mm dia x H 700mmthe bag should be made up of Heavy-duty nylon
cloth. Construction: Two horizontal rings of 500mm dia made up of 20mm x 4mm thick
stainless steel flat with three vertical supports of 25 mm dia x 1.2 mm stainless steel tubes
mounted on 100mm dia rubber castors duly powder coated with PVC caps. Each 8
MULTIPURPOSE STOOL: -
Construction: The top should be made up of 304-grade stainless steel sheet 0.9mm
thick double press bent on four sides. Theedges of the stainless steel sheet should be
folded to 180 degree to avoid the sharp edges. Frame Work: the frame should be made
up of 25mm x 25mm x 1.2mm thick CRCA square tubes for vertical members and the
horizontal members should be made up of 19mm dia x 1.2 thick CRCA tubes. The
stainless steel top should be fixed with the help of pop refits in slush position. The heavy
duly insertable plastic shoes should be provided.
Finish: All components should be pretreated in separate eight-tank process for better
finish good adhesion and corrosion protection. Process includes hot degreasing,
Derusting, activation,Phosphating & No's of water inses as per IS 3618-1966 class 'C'
type and then pretreated materials is coated with epoxy powder with film thickness of
60 microns(approx) and than oven backed at 180 degree centigrade.
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The ring made up of 12.5 mm dia Stainless Steel tube should be fitted on the base to
support the legs. The stool should be fitted with 150mm dia Twin Roller Castor.
280mm/ 510 mm step height and size approx 460 mm L x 300 mm W MS tubular
construction with 18 g CRCA sheet. Steps super imposed by aluminum chucked plate &
legs fitted with rubber feet. Finish: All components should be pretreated in separate
eight tank process for better finish, good adhesion and corrosion protection. Process
includes Hot Degreasing, Derusting, Activation, Phosphating & No’s of Water rinses as
per IS 3618 - 1966 class ‘C’ type and then pretreated materials is coated with epoxy
powder with film thickness of 60 microns (approx.) and then oven baked at 180 degree
centigrade.
280mm step height and size approx 460 mm L x 300 mm W MS tubular construction
with 18 g CRCA sheet. Step super imposed by aluminum chucked plate & legs fitted with
rubber feet. Finish: All components should be pretreated in separate eight tank process
for better finish, good adhesion and corrosion protection. Process includes Hot
Degreasing, Derusting, Activation, Phosphating & No’s of Water rinses as per IS 3618 -
1966 class ‘C’ type and then pretreated materials is coated with epoxy powder with film
thickness of 60 microns (approx.) and then oven baked at 180 degree centigrade.
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ratchet and sliding arrangement for cassette holder. The trolley should have oxygen
cylinder attachment.
Construction: It should be made up of 12.5 x 1.2 mm thick CRCA tube of 44” Length
with a hook to hold mosquito net. Finish: All components should be pretreated in
separated in separate eighttank process for better finish, good adhesion and corrosion
protection. Process includes Hot Degreasing, Derusting Activation, Phosphating & No's of
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water rinses as per IS 3618 - 1966 class 'C' type and then pretreated materials is coated with
epoxy powder with film thickness of minimum 60 microns and then oven backed at 1800 C.
Overall Approx size: Top 300 mm Dia with height adjustable 510mm to 710 mm
Construction: Top should be made up of Stainless Steel & edges duly fold. Base should
be made up of five Horizontal supports of 25mm x 50 mm x 1mm thick rectangular
tubes and the vertical members should be made up of 50 mm Dia x 1.2 mm thick
stainless steel Tubes. In which the square treated screw of 25 mm dia and nut should be
fitted. The nut should have grease pocket to hold the grease. The round Stainless Steel
Top should be riveted on rin made up of 20mm x 3mm MS flat & the cross made up of
25 mm x 25mm square tubes. It should be fitted with stainless steel back support. The
ring made up of 12.5 mm dia Stainless Steel tube should be fitted on the base to support
the legs. The stool should be fitted with heavy duty Rubber at the base.
All components should be pretreated in separate eight-tank process for better finish,
good adhesion and corrosion protection. Process includes Hot Degreasing, Derusting,
Activation, Phosphating & No’s of Water rinses as per IS 3618 - 1966 class ‘C’ type and
then pretreated materials is coated with epoxy powder with film thickness of 60
microns (approx.) and then oven baked at 180 degree centigrade.
16. Wheel Chair
Specification
Overall Width: 24” or 61cms
Foldable width: 11 ½” or 29.5cms
Width of Seat: 17 1/24” or 44cms
Depth of seat: 16” or 41cms
Height of seat from floor: 18” or 47cms
Overall length: 42” or 107cms
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Dimensions +- ½” or 12mm
New foldable wheelchair for use at home and in hospital or rehabilitation centers, for
use on any smooth surface only. Double ball bearings ensure smooth rolling swinging
detachable adjustable footrests positive lock toggle brakes. Strong construction for
convenient handling Electro statically applied powder coating
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pests from entering. Automatic airless electrostatic painting using alkyd amino pain
provides a smooth, scratch resistant surface.
Overall size minimum height 6feet width 3feet Prime quality cold rolled, close-
annealed steel is treated with unique seven stop anti-corrosion process for extra
durability the multi bend seamless construction ensures rigidity and prevents pests
from entering. Automatic airless electrostatic painting using alkyd amino pain provides
a smooth, scratch resistant surface.
1.1 ICU Beds are required in the Intensive Care for comfort of the patient and
to facilitate comfortable transfer to and fro emergency/OT/Wards etc. It
is also required to carry out point of care procedures including
radiological procedures at the bedside.
2 Operational Requirements
2.1 The system should be mechanically operable and adjustable for heights,
trendelenburg etc. It should also be having radiotransluscent top for
carrying out X-Ray at the bedside
3 Technical Specifications
3.1 Bed top:- bed should consist of four sections namely : head section, fixed
section , center section and leg section. It shall satisfy the following
requirements
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adjustment by separate screw mechanism with thrust bearing and
proper lubrication.
e. Bed’s up& down motion with patient load should be light and must
be fitted with high tension spring support system. Adjustment by
separate screw mechanism with thrust bearing and proper
lubrication.
3.2 Section made of CRCA sheet at least 1.25 mm thick , uniformly perforated
full fowler position except head section. The outer tube dia of top section
of backrest and leg rest shall be at least 1.6 mm x 25.4 mm dia.
3.3 Castor wheels of 4- 6 inches with two foot operated locking mechanism.
3.4 Oxygen cylinder carrying facility under the base frame and urinal bottle
holder.
3.5 The mattress shall be ISI 1741 1960 extra hard with grooves covered with
Rexene (Bhorl Polynova). Thickness of Rexene not less than 0.65 mm or
above.
3.7 Nuts and bolts ;- all fasteners like nut bolts etc should be supplied in
electrogalvanized condition of protection against industrial atmosphere.
3.8 Slide railing :- both sides of the rail shall be provided with stainless steel
detachable and collapsible full length made of at least 19 mm dia x 1.25
mm thick . stainless steel tubes housed in M.S. rectangular frame. Railing
shall be below the mattress level once collapsed.
3.9 Rectangular Tubes (CRCA) for outer frame at least 60 mm x 1.6 mm thick
and horizontal transverse members at least19mm x 38 mm x 1.6 mm
thick. Four separate screw mechanism shall be used to achieve back rest
adjustment , knee rest adjustment , trendelberg and position and height
adjustment. Back rest horizontal and knee rest horizontal members of at
least 50 mm x 25 mm x 1.6 mm for chariot base frame of at least 60 mm x
30 mm x 1.6 mm thick. Chariot base shall be joined with main frame work
with connecting brackets and screw mechanism. Chariot based frame
shall have rectangular frame to receive castors. It shall be vertical
members of round tube to receive castor wheels and also materials used
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at least 50 mm x 6 mm for linkage flat at least 40 mm x 8 mm for long flats
and screw holder flat of at least 32 mm x 5 mm.
3.10 Round Bows:- for bows out members at least 31.75 mm dia x 1.25 mm
thick stainless steel tube 304 quality fitted with laminated panel with
board with help of stainless steel brackets , the thickness of laminated
panel board not less the 18 mm . Bows shall consist of outer tubes in one
piece double bend to achieve bow shape and should be detachable for
easy access to patients.
3.11 Buffer:- Rubber Buffer on all the four corners to provide damper effect.
3.12 Finish :- All the components should be free of rust and should have
received anti corrosion treatment and (white / Cream colour) epoxy
powder coating finish. Thickness of coating should not be less than 50
micron and oven baked at 180 degree to 200 degree Celsius. The finish
should exclude stainless steel parts, some hard ware, rubber PVC , castor
wheel if any.
3.13 Dimensions of bed :
Length : 2250 + 5 mm
Width : 1050 + 5 mm
Adjustable height : 225-840 mm
Mattress Size : appropriate as per bed size
5 Environmental factors
6.3 Should have local service facility .The service provider should have the
necessary equipments recommended by the manufacturer to carry out
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preventive maintenance test as per guidelines provided in the
service/maintenance manual.
6.4 Comprehensive warranty for 5 years and provision of AMC for next 5
years.
7 Documentation to be provided
7.3 List of important spare parts and accessories with their part number and
costing
7.4 Log book with instruction for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital technician and
company service engineer should be clearly spelt out
7.7 Must submit user list and performance report within last 5 years from
major hospital
22. Table/Trolley
7. The welding will be with TIG argon arc, smooth finished and
polished with mat finish
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2. CLEAN UP COUNTER (WASH STATION) WITH DOUBLE SINK, ONE
MIDDLE PLATFORM AND FLASH BACK
3. The sinks will be made of S.S. 304; 16 SWG with inside ground and
polished
4. The legs will be of S.S. 304 square pipe 40 x 40 mm; 16 SWG and
will also have nylon bullets for adjustment
5. The corners will be rounded and the bottom pitched to the drain
8. The welding will be with TIG Argon arc, fine polished and finally
with mat finish
3. The sink will be made of S.S. 304; 16 SWG with inside ground and
polished
4. The legs will be of S.S. 304 square pipe 40 x 40 mm; 16 SWG and
will also have nylon bullets for adjustment
5. The corners will be rounded and the bottom pitched to the drain
8. The welding will be with TIG Argon arc, fine polished and finally
with mat finish
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2. The top will be of S.S. 304 grade, 16 SWG sheet
7. The welding will be with TIG argon arc, smooth finished and
polished with mat finish
7. It will also have 5" size castor wheels (4 Nos.); swiveling type - 2
Nos. with brakes and 2 Nos. without brakes
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2. The top will be of S.S. 304 grade, 16 SWG sheet
6. The welding will be with TIG argon arc, smooth finished and
polished with mat finish
3. The legs will be of S.S. 304 square pipe, 40 x 40 mm; 16 SWG and
will also have nylon bullets for adjustment
7. The welding will be with TIG Argon arc, fine polished and finally
with mat finish
2. The complete trolley will be made of S.S. 304 grade, 18 SWG sheet
7. It will also have 4" size castor wheels (4 Nos.); swiveling type - 2 Nos.
with brakes and 2 Nos. without brakes
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10. INSTRUMENT TRAYS - PERFORATED TYPE WITH HANDLE
4. All the joints will be TIG welded, seamless finish, fine polished and
finally finished with electro polish
2. Should have the facility to take X Rays from positions along the
entire length of the trolley and from almost all the entire width of
the trolley.
8. Should have facility to fix IV rods at all the four corners and middle
of mattress base frame.
10. Should have place for fixing ‘B’ Type Oxygen Cylinder.
12. Dimensions
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i. Max. Length : 2000-2100 mm
1. Length- 444 - 405 mm, width 400 - 405mm. Height- 810 - 820 mm.
the outside diameter of the legs of the locker should be 25.4 mm
and thickness of 1.22 mm. Thickness of top should be 1 mm S.S
sheet of 20 G is bent: edge beaded and superimposed of M.S. top.
3. Cabinet-Top and sides- the top and sides of the cabinet should be
made from 1 piece of steel sheet. It should be welded with the back
and the bottom, which are also made from press bent sheets.
5. Knob- the door should be riveted with chrome plated brass knob
which should have the latch carn, by turning knob the door can be
locked.
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13. I.V. STAND
2. Main Frame : Strong & Sturdy five legged neatly made base
mounted on five 2.5cm dia swiveling ball castors of good quality
S.S. double hocked I.V. rod & S.S. tube spring loaded.
5. Process includes
i. Hot Degreasing,
ii. De rusting,
iii. Activation,
7. Dimensions +- ½” or 12mm
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8. Double ball bearings ensure smooth rolling swinging detachable
adjustable footrests positive lock toggle brakes.
Construction:
9. The stool should be fitted with heavy duty Rubber at the base.
2. SS tubular frame.
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6. Complete with corner buffers, powder coated oxygen cylinder
holder, SS IV rod and SS shelves.
5. Dimensions :
6. Table top 60 x 70 cm
7. Height 85 cm.
Finish: All components should be pretreated in separate eight tank process for
better finish, good adhesion and corrosion protection. Process includes Hot
Degreasing, Derusting, Activation, Phosphating & No’s of Water rinses as per IS
3618 - 1966 class ‘C’ type and then pretreated materials is coated with epoxy
powder with film thickness of 60 microns (approx.) and then oven baked at 180
degree centigrade
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EQUIPMENT CSSD-2
2. Operational Requirements
3. Technical Specifications
3.2 Should equip with two dosing pump of chemical / detergent products
under a complete micro-processor control. Dosage of liquid detergent
should be carried out automatically by means of a pump and can
easily be regulated for agents with varying concentration
3.5 The hot and cold water connections should have check valves, back
valves, mud filters and siphonage protection. The Machine should
have its own integrated water heater so that the machine can
function properly in absence of external warm water source
3.6 Water should be taken into the chamber directly to avoid separate
cleaning and disinfection of integrated water tanks.
3.8 Should have at least three factory preset programs and at least two
user selectable programs. The program should be available for
selection at the touch of a button.
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3.9 Control panel should have LED/LCD indications for cycle selection ,
phase indication ,remaining program time indication ,cycle complete
indication, digital temperature reading, and fault indications.
5. Environmental factors
6. Power Supply
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7.1 Should be compliant to ISO 13485: Quality systems - Medical devices -
Particular requirements for the application of ISO 9001 applicable to
manufacturers and service providers that perform their own design
activities.
7.3 Comprehensive warranty for 2 years and 5 years AMC after warranty
8. Documentation
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
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2. Equipment Specifications for Washer Disinfectors (High
Capacity)
1. Description of Function
2. Operational Requirements
2.1 High capacity washer disinfector with minimal floor space is required
for CSSD.
3. Technical Specifications
3.2 Should equip with two dosing pump of chemical / detergent products
under a complete micro-processor control. Dosage of liquid detergent
should be carried out automatically by means of a pump and can easily
be regulated for agents with varying concentration
3.3 The construction of the body should be high quality polished Stainless
Steel AIAI 304 and the internal chamber should be made up of acid-
resistant AISI 316 stainless steel,
3.5 The hot and cold water connections should have check valves, back
valves, mud filters and siphonage protection.
3.6 Water should be taken into the chamber directly to avoid separate
cleaning and disinfection of integrated water tanks.
3.7 High efficiency dryer with a pre-filter and a HEPA filter Class H13/14
3.9 TFT / LCD Touch-screen colour control panel and information display
cycle selection , phase indication as text,remaining program time
indication ,cycle complete indication as text and with a green led,
pressure graph,temperature graph,fault indication
3.10 Multi-level access code system with Special codes for: user,
maintenance, authorized person should be there.
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3.11 Integrated printer
3.12 Should be able to insert and download User identification and load
tracking data can into full tracking data systems by a bar code reader.
3.13 Should be able to review the operation online, download the process
data into server or PC by using a Flash Memory Card, or a direct
Ethernet line.
3.15 Should have separate connections for Cold, Warm and Demineralized
water. The Machine should have its own integrated water heater so
that the machine can function properly in absence of external warm
water source
3.16 Should have rails to accomodate up to eight racks for different types of
loads.
3.18 Should be provided with 5 rotating wash arms with removable caps
facilitating easy cleaning of the inner surfaces of the wash arm. Wash
arms can be removed without any tools.
3.19 Should have at least three factory preset programs and at least two
user selectable programs. The program should be available for
selection at the touch of a button.
26
7. Narrowmesh internal basket of app 70, 35 and 15 liters.with
LID -03( 01 of each size with Lid)
5. Environmental factors
6. Power Supply
7.3 Should be equipped with the highest level - Class C -independent, full
process verification recording system.The critical process values i.e.
temperatures,times, pressures, detergent dosage time, flow & volume,
errors,as well as descriptive cycledata can be independently recorded
by three different means for Quality Assurance System.
8. Documentation
8.4 List of important spare parts and accessories with their part number
and costing.
27
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job descriptin of the hospital technician and
company service engineer should be clearly spelt out.
6. Sterilization cycles: The autoclave residence time should not be les than 60
minutes if the autoclave operates at the working temperature (inner
chamber) of 121°C at a pressure of 15 pounds per square inch (psi) and
should be adjustable as per standards at different temperature and
pressure.
8. Autoclave should be properly equipped with door safety locks, steam traps,
pressure gauges and safety valves for chamber and jacket.
9. Autoclave should have insulation jacket with glass wool, covered with
aluminum foil.
10. The unit should have integral alarms that ring, flash, or otherwise display
information when temperature set-points are exceeded or fall below.
12. The unit includes a data logger or chart recorder for monitoring operational
history.
13. Integral controls, keypad, and/or display on the panel of the unit. The
control panel must document all cycle information including key transition
points in the cycle, alarms and deviations that may jeopardize the
sterilization process, resulting in inadequate sterilization.
28
14. The Sterilizer should be supported on a steel stand, appropriately, coated
for corrosion protection.
17. Carriage trolley with at least three SS trays and roller shelves.
18. The firm should provide all piping connections made up of SS required in
the installation and should install the machine at the identified site in the
Hospital.
4. Flash Sterilizer
4. Chamber shall be fabricated from stainless steel 304 with high quality
argon welding.
5. It will have stainless steel 316L racks for easy loading & unloading
6. It will have high vacuum ejector to ensure effective air removal for
excellent steam penetration & efficient post sterilization drying.
10. There should be alarm when the water in the chamber is low & there
should be process cut off facility when this happens.
29
indicator, Sterilization complete indicator, Emergency Exhaust Switch,
Automatic preheating programme.
5. ETO Steriliser
1. The ETO sterilizer should be of 8 Cubic Feet Capacity.
2. The system should work with 100% ETO .
3. ETO Gas should be provided in Cartridges clearly marked “100% ETO”
and should be approved by ‘EPA’, ‘FDA’ and OSHA for safety and quality.
4. Shall be Microprocessor controlled with Digital Printer.
5. Microcomputer shall monitor & control system operations & functions.
6. Sterilizer Should Have A Built In Aerator.
7. Machine should operate at a negative Pressure (of At least Upto
200mm Of Hg) during Operation.
8. Machine Should Operate at Dual Temperature at 37oC and 55oC.
9. Should Operate In 3 Phase: Pre-Conditioning, Exposure, and Aeration.
10. Total Sterilization Cycle Time Not To Exceed 5.75 Hrs for Warm Cycle
And 7.75 Hrs for A Cool Cycle.
11. Should Be Provided With An alphanumeric display and Graphical
Printer.
12. The system should have a soft touch buttons for operations and
programming, flushed to the surface of the system and not rotating
knobs.
13. Video Screen Display to Check Cycle Status.
14. Continuous RH Display on Screen for Humidity level inside the chamber.
15. Built In Local Exhaust For Removal Of Residual ETO.
16. System should have a self-diagnosis for errors.
17. Compressor should be included in case there is no provision for
Compressed Air Line for the equipment.
18. Standard international safety measure such as locking of door (cannot
be opened during operation either by accident or intend by un-
authorized personnel) for occupational and Fire hazards.
19. An independent body should certify system for compliance with
OSHA Regulation for Safety.
20. Installation to include complete Copper Ducting from the CSSD to the
Hospital Building Terrance and to be left 10 Feet beyond in
Atmosphere.
21. The tender has to guarantee supply of GAS at least for a period of
10years. Certificate from at least 20 existing users required for
satisfactory usage and supply of gas.
30
22. Detailed cost of consumables, such as gas, indicators, sterilization bags,
or any other such items required need to specify clearly.
1. Construction: External AISI 304 stainless steel and Internal AISI 304 or
AISI 316Ti (20/10)
6. Should provide for Water load, water drain and water leveling
operations.
8. Should have alarm and safety features for water level control, cover
closure control, water temperature control, sensor failure control.
10. Automatic water drain after selected number of cycles (from 1 to 99) or
function excluded.
31
ii. 16 keys control keyboard
iii. Water level (min, max, over) and cover closure light indicators
7. Drying Cabinet
0 2. Sound and heat insulated double walls of the cabinet should made of
AIS304 stainless steel.
5 10. System should be complete with high quality air filter, ventilation
connection sleeve,
0 11. Should be vertical system and should occupy not more than 1 sq. meter
of floor space.
2 15. Price for additional wire shelf for future should be made available.
32
8. Sealing Machine: Plain Sealer
1 1. Smooth easy cleaning surfaces
0 2. Ergonomic handling with anti fatigue movement 3.
1 3. Should have automatic sealing indicator
2 4. Quick sealing time with sealing width of 12mm
3 5. Should be microprocessor controlled and with constant temperature 6.
4 6. Should be provided with roll stand
0 7. It should be a table top system
5 8. Should work on 230V, 50 Hz electric power supply.
6 9. Compact system with app 50cm x 20cm x 40cm (±2cm)
Description chamber jacket, cover, end ring, door, water tank, heater plate & ring, of
316 quality SS sheet made of SS all pipes joints & valve made of SS/brass working
pressure 34psi working temperature 131deg C. hydraulic test 440V, 3 phase, AC supply,
50 cycle. operating voltage electrical load 18Kw/36KW , sterilization period, 6 to
8minute
33
EQUIPMENT ENDO N LAPRO -3
1. Equipment Specifications for Video Thoracoscope
1 Description of Function
1.1 A Thoracoscope is a thin, tube-like rigid endoscope instrument
with a light and a lens for viewing.
2 Operational Requirements
2.1 Thoracoscope with video processing and monitoring is required
3 Technical Specifications
3.1 SPECS OF SCOPE:
1. Direction of view should be zero degree.
2. Minimum of 100 degree (app) of field of view.
3. Range of observation from 5 mm to 90 mm.(app)
4. Angulations of tip not less than 200 deg(Up) and 90 deg
(down)with right to left movement of minimum 100 deg.
(app)
5. Insertion tube outer diameter of less than 8 mm with a
working length of not less than 250 mms.
6. Distal end of less than 8 mm.
7. Instrument channel of more than 2.5 mm
8. Compatible with the video system specified.
3.2 Video processor with light source & Monitor
1. Power supply 200-240 V A/C
2. PAL type video signal. The camera should be 3 chips CCD
with high definition (HD) Output with provision of
recording on hard disk, mini DV: disk or tape.
3. Controls for color adjustment, to enhancement and
balance settings.
4. Controls to freeze images enhance a portion of frozen image
(zoom & post-processing).
5. Patient and physician data input keyboard.
6. Operates on Xenon lamp.
7. Emergency lamp.
8. Compatibility with the gastro scope and colonoscope
duodenoscope and Enteroscope
9. 19” LCD color monitor with XGA resolution.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 1. Rod lens Telescope 0 degree 10mm , Length 31 cm
2. Rod Lens Telescope 30 degree 10mm, Length 31 cm
3. Trocar 6mm with blunt tip flexible cannula and silicone
leaflet valve
4. Trocar 9mm with blunt tip flexible cannula and silicone
leaflet valve
5. Trocar size 11mm with blunt tip flexible cannula and
silicone leaflet valve
6. Trocar size 11mm with blunt tip cannula with thread
7. Manhes dissecting and grasping forceps size 5mm
8. Kelly dissecting and grasping forceps size 5mm
34
9. Babcock grasping forceps size 5mm
10. Bowel grasper rotating 5mm
11. Scissors rotating with connector pin, spoon blades, double
actionjaw, size 5mm
12. Scissors rotating serrated, curved, conical and double action
jaw size 5mm
13. Micro hook scissors and single action jaw, size 5mm
14. Scissors dismantling rotating serrated, single action jaws
bayonet shaped size 5mm
15. Needle driver Parrat-Jaw straight handle with ratchet
length 33 cm
16. Assistant Needle driver Flamingo Jaw straight handle length
33 cm
17. Manhaes grasping forceps rotating size 5mm atraumatic
single action jaws
18. Suction & irrigation with two way stop cock
19. Bipolar & Monopolar high frequency cord with 5mm plug
20. 3 Chips Camera PAL having Digital Imaging Processor
21. Cold Light fountain Xenon 175 power supply 100-125 /
220-240VAC, 50/60 Hz complete
22. TFT Monitor PAL 19”(inch) maximum resolution
1280x1024
23. Video Cart
24. Fiber Optic cable
25. 0 degree, 30 degree & 60 degree upward & downward
angulated Rongeur forceps 33 cm shaft.
26. 90 degree & 45 degree punch with 30 cm shaft.
27. Clip Applicator 5 mm & 10 mm.
28. Fan Retractor.
29. Endo GI stapler for stapling Bronchi & Vessels.
30. Needle Holder 5 mm & 33 cm long.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
7.2 Shall be certified to be meeting safety standard IEC 60601-2-18
part 2 Particular requirements for the safety of endoscopic
equipment.
7.3 Manufactures/Supplier should have ISO certificate to Quality
Standard.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
35
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
maintenance support as per manufacturer documentation in
service / technical manual.
8.4 List of important spare parts and accessories with their part
number and costing
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
36
Electro Mechanical tissue morcellator with changeable
blades for use in morcellation and removal of tissue
postprostate enucleation. Should include morcelloscope
complete set, control box, handpiece, 2 sets of blades,
suction device and cleaning brushes.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0-50deg C and relative humidity of 15-90%
5.2 Thu unit shall be capable of operating in ambient temperature of
20-30 deg C and relative humidity of less than 70%
5.3 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC; EMC-directive.
6 Power Supply
6.1 Power input to be 220-240 VAC, 50Hz fitted with Indian plug
6.2 Resettable overcurrent breaker shall be fitted for protection
6.3 Voltage corrector/stabilizer of appropriate ratings meeting ISI
Specifications.( Input 160-260 V and output 220-240 V and 50 Hz)
6.4 Suitable UPS with maintenance free batteries for minimum one-
hour backup should be supplied with the system.
7 Standards, Safety and Training
7.1 Manufactures/Supplier should have ISO certificate to Quality
Standard.
7.2 Should be compliant with IEC 61010-1:(or any international
equivalent eg EN/UL 61010) covering safety requirements for
electrical equipment for measurement control and laboratory use
7.3 Should be FDA , CE,UL or BIS approved product
7.4 Comprehensive training for lab staff and support services till
familiarity with the system.
7.5 Comprehensive warranty for 2 years and 5 years AMC after
warranty
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
maintenance support as per manufacturer documentation in
service / technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
8.6 Compliance Report to be submitted in a tabulated and point wise
manner clearly mentioning the page/para number of original
catalogue/data sheet. Any point ,if not substantiated with
authenticated catalogue/manual, will not be considered.
37
3. Equipment Specifications for ULTRASONIC ASPIRATOR
1 Description of Function
1.1 Ultrasonic aspirators use mechanical ultrasonic vibration and an
irrigation/suction system to fragment and remove soft tissue and
high-watercontent growths from various parts of the body.
2 Operational Requirements
2.1 The system should be quoted with the paediatric as well as adult
handpieces.
3 Technical Specifications
3.1 Surgical aspirator should be based on magneto-restriction or
piezoelectric technology.
3.2 The hand piece must be cool if required to prevent overheating by
coaxial flow of water.
3.3 The hand pieces should be autoclavable and without need to
dismantle for autoclaving.
3.4 The vacuum pump should provide preferable the suction of >
600mm of Hg.
3.5 It should incorporate an Electro-surgical unit fitted on ultrasonic
hand piece for coagultion and cutting function.
3.6 The console unit should house control panel storage for
footswitch, electrical cords and self-contained suction apparatus.
3.7 The unit should include all necessary control preferably color-
coded, which may include amplitude, irrigation, aspiration and
tissue select mode.
3.8 It should have safety features like optical signal for failed hand
pieces and signal for failed unit.
3.9 It should have on and off button.
3.10 It should have integral suction with vacuum pressure of-20 to -90
Kpa. in continuous low noise and digital display.
3.11 It should preferably have 2 liter capacity container of unbreakable
material with level sensor and anti-overflow system.
3.12 Hand piece should be light, preferable 20 KHz and amplitude
should be >130 micrometers
3.13 The hand piece should be able to accommodate selection of tips for
wide range of applications. It should have inbuilt water cooling
system &also should be able to differentiate tissue barriers with
tactile feedback. It should be sterilizable by autoclave and ethylene
oxide. Both curved & straight hand piece should be available.
3.14 The internal diameter of tips should range form 1.0 to 2.0mm.
3.15 The irrigation pump should be inbuilt in the unit, the irrigation
output 0- 65ml/min.
3.16 All hand-pieces/ instruments should be detachable.
4 System Configuration Accessories, spares and consumables
4.1 ACCESSORIES:
1. Trolley with suction canister.
2. Ultrasonic probe-curved, 2 each of variable length with
extra laproscopic probes 23 KHz and 35 KHz.
3. Assembly kit for aspirator- 1
38
4. Aspirator with 2 liters suction bottle with disposable
secretion bag-1
5. Infusion bottle holder-1
6. Double foot switch-1
7. Cleaning brush for instrument lumen-2
8. Instrument connection cables- 2
9. Suction / irrigation tubing (5meter each), silicon twin tube-
2.
10. Double set of cable and tubing clips- 10sets.
11. Metal puncture tube - 2
12. Sterilizing cassette with silicon mat and textile filter-2.
4.2 CONSUMABLES:
1. Textile filters for sterilizing cassette-10 pieces.
2. Suction/ Irrigation tubing (5 meter each) - 10 pieces.
3. Cable and tube clips - 5X 10 pieces.
4. Suction and Irrigation tubing, silicon twin tube (4.5 meters
each) – 5 pieces
5. Disposable secretion bags 2 liters- 2 pieces.
6. Connection nipple, suction tube / secretion reservoir - 5
pieces.
7. Internal flushing tube - 5 pieces.
8. Protective cover-4 pieces.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0-50deg C and relative humidity of 15-90%
5.2 Thu unit shall be capable of operating in ambient temperature of
20-30 deg C and relative humidity of less than 70%
5.3 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC; EMC-directive.
6 Power Supply
6.1 Power input to be 220-240 VAC, 50Hz fitted with Indian plug
6.2 Resettable overcurrent breaker shall be fitted for protection
6.3 Voltage corrector/stabilizer of appropriate ratings meeting ISI
Specifications.( Input 160-260 V and output 220-240 V and 50Hz)
6.4 Suitable UPS with maintenance free batteries for minimum one-
hour backup should be supplied with the system.
7 Standards, Safety and Training
7.1 Manufactures/Supplier should have ISO certificate to Quality
Standard.
7.2 Should be compliant with IEC 61010-1:(or any international
equivalent eg EN/UL 61010) covering safety requirements for
electrical equipment for measurement control and laboratory use
7.3 Should be FDA , CE,UL or BIS approved product
7.4 Comprehensive training for lab staff and support services till
familiarity with the system.
7.5 Comprehensive warranty for 2 years and 5 years AMC after
warranty
8 Documentation
39
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
maintenance support as per manufacturer documentation in
service / technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
8.6 Compliance Report to be submitted in a tabulated and point wise
manner clearly mentioning the page/para number of original
catalogue/data sheet.Any point ,if not substantiated with
authenticated catalogue/manual, will not be considered.
40
Monitor
19’’ Flat Panel Monitor Colour
Insufflator
40Liter of high flow
Microprocessor controlled unit
Soft Approach Pressure control for safe recovery of abdominal pressure
Gas heating
LCD based central display monitor with multilingual text & graphics AV
warning signal
Laparoscopes, Fully Autoclavable with working length 300mm
Wide angled distortion free view
Universal adaptor for other light sources
Yellow Glass index for optimum evenness of focus & contrast
0 degree, 10mm
30 degree, 10 mm
0 degree , 5mm
Flexible video telescope
Specifications
Laparoscopic hand instruments (reusable) with 310mm working length,
take apart locking / unlocking mechanism, rotable with interchangeable
handle with monoploar diathermy attachment ( Except trocars and veress
needle)
Vass needle 12 cm length
Varss needle 15 cm length
Carbon-di-oxide gas tubing
Trocars sleeves 11 mm
Reducer 11/5 mm44442
Trocars sleeves 5.5 mm 4
Trocars (pyramidal tip) 10 mm 4
Trocars (pyramidal tip) 5 mm 4
Trocars washer 5 mm 100
Trocars washer mm 50
Laproscopic biopsy forceps 5 mm,
Maryland dissector 5mm with unipolar diathermy22
Maryland dissector 5mm, high performance with bipolarcutting2
Atraumatic graspers, 5mm 2
Metzenbaum scissors (5cm) with unipolar diathermy
Metzenbaum scissors (5cm) high performance with bipolarcutting22
Fan retractors 5 mm 2
Laproscopic cautery lead 4
Suction irrigation device with two way valve 2
L shaped hook electrode 5mm
L shaped hook 5mm , high performance with bipolar cutting2
Laproscopic bowel grasper 5mm, length 33-36 cm
Laproscopic spoon forceps 10mm length 33- 36 cm22
Needle holder 5mm, 33 cm long 4
Laproscopic suction cannuala, 10 mm
Laparoscopic suction cannula 5 mm22
Clip applicator 10 mm Large, Medium, Small Clips
41
Gall bladder extraction 5mm Large, Medium, Small Clips
Hassan cannula
Lap Eondotrainer
Port closure needle
Sterilization tray with cover 3 x 1
42
Maximum Flow Rate of Pump :app: 170ml/10sec
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 1. Biopsy forceps :3 each
2. Foreign body grasper (basket type) 2
3. Polypectomy snare:2
4. Standard tip canula:2 types – 10 ea
5. Sphincterotome for side viewing duodenoscope only (wire
guided, triple lumen) – 10
6. Mechanical lithotripter :5
7. Polypectomy cautery system :1
8. Guide wires 2 types ( 0.025 “F, 0.035 “ in diameterF); length
450 cm, nonkinkable with stripes to detect movement – 5
9. Basket for retieving stones with memory filaments – 5
10. Balloons 11mm diameter and wire guided – 5
11. Single pigtail stents – 7 cm, 10 cm long; 7 F and 10 F
diameter – each 10
12. Stents – straight 7 F and 10F; 7 cm and 10 cm long – each
10 in number
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Shall be certified to be meeting safety standard IEC 60601-2-18
part 2 Particular requirements for the safety of endoscopic
equipment.
7.2 Should be FDA , CE,UL or BIS approved product
7.3 Comprehensive warranty for 2 years and 5 years AMC after
warranty.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.6 User list to be provided with performance certificate.
43
6. Equipment Specifications for Video Enteroscope (Double
balloon)
1 Description of Function
1.1 Double-Balloon Endoscopy System allows ease of insertion and
makes not only diagnosis but also treatment of the entire small
intestine a reality.
2 Operational Requirements
2.1 Enteroscope should be compatible with the commonly used
light sources.
3 Technical Specifications
3.1 Direction of View: Forward Observation Range app: 6~100mm
Field of View min 140 Degrees Specifications Enteroscope: Distal
End Diameter app: 9.5 mm Flexible Portion Diameter app: 9.2 mm
Bending Capability (Up/Down) 180 Degrees / 180 Degrees
Bending Capability (Left/Right) at least 150 Degrees / 150
Degrees Forceps Channel Diameter more than 2.5mm
Working Length not less than 2,000mm Video output to be
compatible with the video processor specified.
3.2 Video processor with light source & Monitor
1. Power supply 200-240 V A/C
2. PAL type video signal.
3. Controls for color adjustment, to enhancement and balance
settings.
4. Controls to freeze images, enhance a portion of frozen
image (zoom &post-processing).
5. Patient and physician data input key board..
6. Operates on Xenon lamp.
7. Emergency lamp.
8. Compatibility with the gastro scope and colonoscope
duodenoscopE and Enteroscope
9. 15” LCD colour monitor with XGA resolution.
3.3 Over-tube Specifications :
Outer Diameter app:13.2mm
Inner Diameter app:10.8mm
Distal End Diameter app: 9.8mm
Outer Diameter (Balloon) : 40mm
Working Length app:1,350mm
3.4 Balloon Pump Controller with Remote Switch Specifications
Set Pressure of Balloon app : 5.5kpa+/-2kpa
Maximum Flow Rate of Pump :app: 170ml/10sec
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 1. Biopsy forceps :3 each
2. Foreign body grasper (basket type) 2
3. Polypectomy snare:2
4. Standard tip canula:2 types – 10 ea
5. Sphincterotome for side viewing duodenoscope only (wire
guided, triple lumen) – 10
44
6. Mechanical lithotripter :5
7. Polypectomy cautery system :1
8. Guide wires 2 types ( 0.025 “F, 0.035 “F in diameter); length
450 cm, nonkinkable
with stripes to detect movement – 5
9. Basket for retieving stones with memory filaments – 5
10. Balloons 11mm diameter and wire guided – 5
11. Double pigtail stents – 7 cm, 10 cm long; 7 F and 10 F
diameter – each 10
12. Stents – straight 7 F and 10F; 7 cm and 10 cm long – each
10 in number
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Shall be certified to be meeting safety standard IEC 60601-2-18
part 2 Particular requirements for the safety of endoscopic
equipment.
7.2 Should be FDA , CE,UL or BIS approved product
7.3 Comprehensive warranty for 2 years and 5 years AMC after
warranty
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.6 User list to be provided with performance certificate.
45
many times so the endoscopist can see small changes in the
tissues.
2 Operational Requirements
2.1 The ERCP scope should also contains channels that allow the
endoscopist to take biopsies and introduce or withdraw fluid, air
and instruments and should be supplied with all accessories.
3 Technical Specifications
3.1 Upper GI Scope (Adult )
1. Direction of view should be zero degree.
2. Minimum of 130 degree of field of view.
3. Range of observation atleast from 5 mm to 90 mm.
4. Angulations of tip up at least 180 degrees and down 90
degrees with right and left movement of at least 100/100
degrees.
5. Insertion tube diameter of less than 10 mm .
6. Distal end diameter of not more than 10.5 mm
7. Instrument channel of more than 2.5 mm
8. Working length of not less than 1000mm
9. Should be compatible with the video system specified
3.2 Upper GI Scope(Pediatrics)
1. Direction of view should be zero degree.
2. Minimum of 130 degree of field of view.
3. Range of observation atleast from 5 mm to 90 mm.
4. Angulations of tip up at least 180 degrees and down 90
degrees with right and left movement of at least 100/100
degrees.
5. Insertion tube diameter of less than 10 mm .
6. Distal end diameter of not more than 10.5 mm
7. Instrument channel of more than 2.5 mm
8. Working length of not less than 1000mm
9. Should be compatible with the video system specified
3.3 Lower GI Scope(Adult)
1. Direction of view should be zero degree.
2. Minimum of 130 degree of field of view.
3. Range of observation at least from 5 mm to 90 mm.
4. Angulations of tip up at least 180 degrees and down 90
degrees with right and left movement of at least 100/100
degrees.
5. Inner diameter optimal
6. Distal end diameter of not more than 10.5 mm
7. Instrument channel of more than 2.5 mm
8. Working length of not less than 2000mm
9. Should be compatible with the video system specified
10. Endotherapy compatible
11. Fully immersible in disinfectant solution
3.4 Lower GI Scope(Pediatric)
1. Direction of view should be zero degree.
2. Minimum of 130 degree of field of view.
3. Range of observation atleast from 5 mm to 90 mm.
46
4. Angulations of tip up at least 180 degrees and down 90
degrees with right and left movement of at least 100/100
degrees.
5. Inner diameter optimal
6. Distal end diameter of not more than 10.5 mm
7. Instrument channel of more than 2.5 mm
8. Working length of not less than 1500mm
9. Should be compatible with the video system specified
10. Endotherapy compatible
11. Fully immersible in disinfectant solution
3.5 DUODENO VIDEOSCOPE (Side viewing for ERCP)
1. Field of vision more than 100 deg.
2. Direction of view 5deg backward / oblilque
3, Depth of view app 5-50 mm
4. Distal end outer diameter not exceeding 13.5
5. Insertion tube outer diameter not exceeding 13 mm
6. Bending angulation should be at least up 120 deg, down 90
deg, Right 110 deg Left 90 deg
7. Working length not below 1200 mm
8. Instrumental channel not less than 4 mm
9. Compatible with video system specified
3.6 Video processor with light source & Monitor
1. Power supply 200-240 V A/C
2. PAL type video signal.
3. Controls for color adjustment, to enhancement and balance
settings.
4. Controls to freeze images, enhance a portion of frozen
image (zoom &post-processing).
5. Patient and physician data input key board..
6. Operates on Xenon lamp.
7. Emergency lamp.
8. Compatibility with the gastro scope and colonoscope
duodenoscope and Enteroscope
9. 15” LCD colour monitor with XGA resolution.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 1. Biopsy forceps :3 each
2. Foreign body grasper (basket type) 2
3. Polypectomy snare:2
4. Standard tip canula:2 types – 10 ea
5. Sphincterotome for side viewing duodenoscope only (wire
guided triple lumen) – 10
6. Mechanical lithotripter :5
7. Polypectomy cautery system :1
8. Guide wires 2 types ( 0.025 “F, 0.035 F“ in diameter );
length 450 cm, non-kinkable with stripes to detect
movement – 5
9. Basket for retrieving stones with memory filaments – 5
10. Balloons 11mm diameter and wire guided – 5
47
11. Double pigtail stents – 7 cm, 10 cm long; 7 F and 10 F
diameter – each10
12. Stents – straight 7 F and 10F; 7 cm and 10 cm long – each
10 in number
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60minutes back up.
7 Standards, Safety and Training
7.1 Shall be certified to be meeting safety standard IEC 60601-2-18
part 2 Particular requirements for the safety of endoscopic
equipment.
7.2 Should be FDA , CE,UL or BIS approved product
7.3 Manufacturer should be ISO certfied for quality standards.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
48
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
49
owner, Customers ID etc. Memorization of : the setting for functions such as Color,
Enhancement, Irish,Selected Setting White balancing etc. retainable when power is
off/on. 11.Xenox Light Source(300 Watts) Automatic Brightness Control : With Servo
Diaphragm Method Internal Memorization battery : For Storing Selected Settings in
Light Source even if the Power is off. Main Lamp : Xenon Short-arc Lamp (300 Watts)
with switching Regulator Mechanism. Main Lamp Life : Appx. 500 hrs on continuos use
Emergency Lamp : Halogen 12V 100 Watts with apprx 100hrs or more life. Power
Supply : 220-240 V Ac,Freq 50/60 Hz,Input Current 3A Weight : Around 15-16 Kg or
less LCD Monitor 14’’ Flat Screen color LCD Monitor(high Resolution)
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 1. Biopsy forceps :3 each
2. Foreign body grasper (basket type) 2
3. Polypectomy snare:2
4. Standard tip canula:2 types – 10 ea
5. Sphincterotome for side viewing duodenoscope only (wire
guided, triple lumen) – 10
6. Mechanical lithotripter :5
7. Polypectomy cautery system :1
8. Guide wires 2 types ( 0.025 “F, 0.035 “ in diameterF); length
450 cm, nonkinkable with stripes to detect movement – 5
9. Basket for retieving stones with memory filaments – 5
10. Balloons 11mm diameter and wire guided – 5
11. Double pigtail stents – 7 cm, 10 cm long; 7 F and 10 F
diameter – each 10
12. Stents – straight 7 F and 10F; 7 cm and 10 cm long – each
10 in number
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply-None
7 Standards, Safety and Training
7.1 Shall be certified to be meeting safety standard IEC 60601-2-18
part 2 Particular requirements for the safety of endoscopic
equipment.
7.2 Should be FDA , CE,UL or BIS approved product
7.3 Manufactures/Supplier should have ISO certificate to Quality
Standard.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
50
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
51
4. Standard tip canula:2 types – 10 ea
5. Sphincterotome for side viewing duodenoscope only (wire
guided triple lumen) – 10
6. Mechanical lithotripter :5
7. Polypectomy cautery system :1
8. Guide wires 2 types ( 0.025 “F, 0.035 F“ in diameter );
length 450 cm,
non-kinkable with stripes to detect movement – 5
9. Basket for retrieving stones with memory filaments – 5
10. Balloons 11mm diameter and wire guided – 5
11. Double pigtail stents – 7 cm, 10 cm long; 7 F and 10 F
diameter – each 10
12. Stents – straight 7 F and 10F; 7 cm and 10 cm long – each
10 in number
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6. 1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Shall be certified to be meeting safety standard IEC 60601-2-18
part 2 Particular requirements for the safety of endoscopic
equipment.
7.2 Should be FDA , CE,UL or BIS approved product
7.3 Manufacturer should be ISO certfied for quality standards.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number andcosting.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
52
EQUIPMENT ICU-4
1. Electric Suction Machine Lipo fully stainless steel body
Rotary High-Vac are double stage pumps of larger capacities, which are knows as
Lipo for fats extraction and full in cosmetics surgery, the main assembly of the pump consist
of a stator with a rotor mounted eccentrically in it. The rotor is fitted with two spring
loaded diametrically opposed vanes, which move in and out of their slots pressing against
the inner surface of the stator these are oil sealed self lubricated, silent running, it is
designed to achieve maximum vacuum in a very short time, it reduce the wear and tear of
its components and makes it suitable for noiseless and trouble free performance for years
and thus helps in reduction of repair bills, these are very compact but so simple in design
that all minor repairs in case of need can be carried out easily, it run continuously for many
hours at a time. The entire pump and motor are placed in an attractive solid STAINLESS
STEEL cabinet having steel top, which is giving extra protection, reduces heat noise and
vibration to the minimum the suction mechanism is oil immersed. The unit is mounted on
smooth moving ball bearing heavy-duty castors, and noiseless. It crates vacuum of 700 to
760mm of Hg (28” to 30”) the suction system is accurately controlled and precisely
regulated by knob this unit is fitted with filter and automatic cut off by float mechanism,
vacuum gauge, pilot light and protection fuse, this unit is fitted with 1/2HP ball bearing
double shaft motor working on 220-250V single phase 50cycle Suction Capacity: 25Lts /p
minutes Max Vacuum: 700mm to 760mm of Hg Consumption: ½ HP Voltage: 220 V 50
Cycles Castors: 5cm Antistatic Weight: Approx 43kg
ideally suited for use in intensive care units out patient clinics emergency room or during
emergency air or land transport mains cum rechargeable batteries power supply battery
back up more than 2 hours bright easy to read large LED display stored data can be recalled
printed or downloaded in PC NIBP display systolic, diastolic and mean pressure, manual
stat or automatic adult and neonatal modes, SPO2 fast reliable and accurate SPO2 tru trak
technology patented by datax ohmeda total operation time approximately 2 hours at room
temperature using Ni-MH batteries microcontroller controlled device automatic self test at
power on automatically continuous system diagnostics visibility from 30feet in dark and 25
feet in ambient light spo2 calibration functional range 0% to 100% accuracy 90% to 100%,
1.5% - 80% to 89.9%, 2.1%, 70% to 79.9%, 2.8% - 60% to 69.9% 3.5%, below 60%
unspecified first reading full accuracy 10 seconds from power on 07 seconds while oxi
meter is on pulse rate range 20 to 255 beats per minute BPM accuracy assuming a constant
pulse rate 1 standard deviation 40 to 235: 1.7% - 20 to 40 and 236 to 255 unspecified first
reading accuracy reduce 5 bpm for 15 seconds then full accuracy 15 seconds from power on
10 seconds while oxi meter is on display spo2 pulse rate, systolic and diastolic three digit
LED numeric display 19m height map temperature perfusion index & interval three digit
LED numeric display 18m height pleth bar pulse rate signal strength a column of
logarithmically scaled eight segments (8 segment LED) NIBP measurement technique
oscillometic method implying stepwise pressure deflation. Proprietary software eliminates
most ambient noise and motion artifact application adult and pediatrics blood pressure
53
range systolic 30-255mm diastolic 15-220mm MAP 20-235mm Alarms audio visual alarms
for high and low spo2 pulse rates systolic diastolic MAP five functional alarms, alarms
audible, till not attended. Accuracy NIBP 5mmhg standard resolution NIBP 1mmhg over
pressure limit 290m hg Measurement modes manual adaptive or preset cuff inflation
automatic host controlled 1-90 minutes as selected by host stat restarts a new
measurements after 5 seconds pause stat mode terminates automatically after 5mints
DATA storage last 50 readings serial interface data lines – Txd and GND baud rates
4800rpm signal level Rs232 compatible Power supply 9volts Ni-MH battery and or 230v
AC mains
3. Anesthesia kit
1) Laryngoscope 4blades with standard handle 2cell 4spare lamps in pouch
code 6204 1set
2) Maggils forceps adult code 7204 1pc
3) Maggils forceps child code 7205 1pc
4) Maggils forceps infant code 7206 1pc
5) Bain Circuit code 2005 1pc
6) Rebrathing bag 0.5liter code 8201B 1pc
7) Rebrathing bag 1liter code 8202B 1pc
8) Rebrathing bag 1.5liter code 8203B 1pc
9) Rebrathing bag 1liter code 8204B 1pc
10) Jackson Rees Peadiatric circuit code 2001 1pc
11) Tube cleaning brush set of 4 code 7200 1pc
12) E.T.Tube Red rubber cuff 5/5.5/6/6.5/7/7.5/8 8.5/9/9.5/10 (set of 11) 1set
13) E.T. Tube red rubber plain2/2.5/3/3.5/4/4.5/5(set7) 1set
14) Rao’s tracheal connectors set in a box code 7009 1set
15) Guedel airway siliconised 000,00,0,1,2,3,4 set of 7 1set
16) Malleable styled with handle set of 3 code 7201 1set
17) Goldman halothane vaporizer stand adaptors code 4001 1pc
54
high/slow speed,Battery charge low etc. Should have air in line removal facility with purge
mode. Should work on mains and battery and minimum 3 hours battery backup. Should
work on KVO Mode. KVO rate should be user selectable between 0.1 ml/hr to 9 ml/hr.
Should work on Micro and Macro standard I.V.sets. Calibration facility for no. of drops per
Ml from front panel. Should have free flow protection feature in case of accidental door
opening. Should work in both modes – Volumetric & Drop counting mode. Should have
nurse call facility with the help of a separate key on the front panel. Should have potential
free contact for remote alarm & Nurse call. Should have fixed drop sensor. The rates should
be stored into memory with facility for memory clear.
55
defibrillation synchronized to the R wave marker indication on ECG waveform sync
message display message on monitor screen and lamp on front panel accessories
defibrillator paddles (adult & pediatric) 1no, disposable electrodes 30 nos. patient cable
(3lead) 1no, mains cable (power cord) 1no, internal paddles 1no, earth cable 1no, accessory
bag 1no, user manual 1no, cardijelly 1bottle
56
2. Hand-piece with in-built transducer & silicon cable
3. Hand-switch activation adopter for blade & hook probe
4. Cart to house the generator and accessories
5. Dual foot-switch attachment
6. Stand-by mode for better safety
7. System diagnostics and troubleshooting guide
8. Warning system for malfunctioning cable, probe etc
9. Power entry filters to suppress electromagnetic
disturbances to monitors
10. It should have dual foot switch receptacles to connect two
footswitches to allow simultaneous use by 2 surgeons.
11. It should have a vibration range of 50-100micrometer.
4 System Configuration Accessories, spares and consumables
4.1 B) Accessories
1. Foot-switch with max and min pedals and cable.
2. 5 mm blade system adopter
3. Hand switch adopter
4. Open Surgery Instruments:
a. Coagulating shears – 10 mm dia, 20 cm long
b. Short Curved Coagulating shears- 5 mm dia, 14 cm
long.
c. Dissecting hook, 5 mm dia,10cm long
d. Hand Activted Coagulting shears with Clicker – 5
mm di ,Curved mode 23 cm long.
5. Endoscopic Surgery Instruments:
a. Dissecting Hook, 5mm dia, 32 cm long.
b. Curved Blade , 5mm dia, 32 cm long.
c. Laparoscopic Coagulating shears , 10mm dia , 34cm
long.
d. Laparoscopic Coagulating shears , 5mm dia ,knife
mode, 34cm long.
e. Laparoscopic Coagulating shears , 5mm dia , curved
mode, 36cm long.
f. Laparoscopic Hand Activated Coagulating shers ,
5mm dia, curved mode, 36 cm long.
g. Laparoscopic Coagulating shears , 5mm dia , Curved
mode, 45cm long.
h. Laparoscopic hand activated Coagulating shears
with clicker -5mm dia curved mode, 36cm long.
C) Probes
1. It Should have both 5 mm & 10 mm instruments.
2. It should have the following types of shears for open &
laparoscopic surgery.
a. 10 mm Coagulating shear capable of working in 3
modes – flat, Blunt & Sharp.
b. 5 mm Laparoscopic Curved coagulating Shears, 360
degree rotable, capable of sealing blood vessels upto
5 mm diameter with clicker & integrated bilateral
57
integrated hand control to enable precise operation
of system by hand.
3. All Hand Pieces should be steam autoclavable.
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 120 minutes back up.
7 Standards, Safety and Training
7.1 The generator must be CF isolated applied device and defibrillator
protection must be available.
7.2 Should be FDA , CE,UL or BIS approved product
7.3 Manufacturer should have ISO certification for quality standards.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Electrical safety conforms to standards for electrical safety IEC-
60601 / IS-13450
7.6 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technicalmanual.
8.4 List of important spare parts and accessories with their part
number andcosting.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
8.6 Compliance Report to be submitted in a tabulated and point wise
manner clearly mentioning the page/para number of original
catalogue/data sheet.Any point ,if not substantiated with
authenticated catalogue/manual, will not beconsidered.
58
12. Equipment Specifications for Cardiopulmonary Exercise
Physiology Test System with Treadmill
1 Description of Function
1.1 Cardiopulmonary exercise testing (CPT) system gives a breath-by-
breath measurement for comprehensive functional analysis of a
subject’s cardiopulmonary, respiratory and metabolic systems.
2 Operational Requirements
2.1 System complete with Treadmill and Analysis software is required.
3 Technical Specifications
3.1 SPECIFICATIONS FOR AN BREATH BY BREATH EXERCISE
PHYSIOLOGY TEST SYSTEM
1) The unit should be a compact unit for spirometry and allied
parameters, mounted on a suitable trolley.
2) The system should measure VO2,VCO2,RQ,VE, spirometry /
flowvolume, AT etc.
3) The system should be interfaced to a PC with the following
specifications– Intel Pentium Core 2 Duo 2.7Ghz and above
PC system with 120 GB HDD , 512 MBRAM , 1.44MB FDD ,
52 x DVD RD/WR drive , Serial /Parallel/USB ports , 17”
Colour LCD/TFT monitor , Keyboard , Mouse.HP colour
inkjet printer
4) The system should have a fully automatic and computerized
volume calibration system.
5) The system should measure Nutritional parameters.
6) The system software should operate under windows XP
environment.
7) The system should have a bidirectional volume sensor with
the following specifications:-
Volume: 0 to 10 lit.
Accuracy: 50 ml or 2%
Resolution: 3 ml
Flow: 0 to 15 l/s
8) System should have oxygen & CO2 analyzer with response
time less than 80 msecs.
9) The system should record data breath by breath and
intrabreath.
10) The system should have a unit to automatically detect
ambient conditions such as pressure, temperature, and
humidity.
11) It should be have a 12 channel ECG unit integrated into the
system.
12) It should be interfaced a treadmill system.
67 (Specifications of treadmill enclosed).
13) A suitable interpretation program to evaluate the test
results should be available.
14) The system should have the following:
a) Bodyplethysmography supplement.
59
b) PFT Supplement: FRC – Helium and Diffusion single
breath
3.2 SPECIFICATION OF TREADMILL
The new generation of treadmills especially designed in
accordance with high safety and quality requirements in Pneumology,
Cardiology, Stress Testing, Endurance Training, Rehabilitation, Sports
Medicine as well as in Medical Fitness Training. The digital interface (RS
232) should allow the treadmill and all its functions being controlled via
an Ergospirometry measuring station or a PC (SW program for control via
virtuel User Terminal to be included). Current values such as speed,
gradient, time, index no., distance as well as pulse rate can be transferred
to the Ergospirometry measuring station. For safety purposes the unit
should be equipped with an emergency switch which stops the treadmill
at any stage of operation, and which switches the WHOLE system
powerless.
Technical Specifications:
Speed:adjustable from 0 - 22 km/h optional: 0 - 30 km/h
Resolution:0.1 km/h; 0.5 %
Gradient: 0 - 24 %: electrical engine brake prevents acceleration
caused by body weight at gradient; optional: reverse operation 0 to -24%
for downhill running (up to 5 km/h)
Resolution: 0.5 %
Acceleration:7 intensities (3 ... 131 sec from 0 to max.) manual or also
selectable via program step
Slow down:7 intensities (3 ... 131 sec from max. to 0) manual or also
selectable via program step
Motor power: 2.2 kW
Motor: maintenance-free and efficient rotary current asynchronic motor
(CE mark) with V-belt, low noise and smooth running
Heart rate measurement: POLAR wireless, 1-channel receiver, beat-to-
beat ECG precise measurement automatic load control according to
preprogrammed heart rate (target pulse)
Interface: RS232 (V 24) incl. PC-, CosRec-, CosCom- ECG, Oxycon and
serial printer protocol
Programs: fixed memory locations incl. test programs Conconi,
Ellestad,Naughton, etc. in combination with User Terminal Platform:
wear-resistant and shock-absorbing
Usable platform area:app 150 x 50 cm (L x W)
Total dimensions: app 210 x 82 x 150 cm (L x W x H)
Weight: app approx. 200 kg
Packing: app 223 x 107 x 83 cm (L x W x H); approx. 294 kg
Handrails:metallic railing in front and at both sides
2. User terminal with HR Measurement
Integrated User Terminal with high contrast LC display. Complete
with POLAR Heart Rate Measurement system and heart rate
dependent load control. Current values such as speed, gradient,
time, index no., distance as well as pulse rate should be legibly
presented on the LCD. Programs should be available with fixed
60
memory locations incl. test programs Conconi, llestad, Naughton,
etc.
3. Following should be should be available
a) Para graphic Software:-
The PC-software package Para Graphics should provide on-line
recording of the load parameters and the heart rate in the form of
graphs on the colour screen. The data should be exported to other
programs (e.g. POLAR, Cyclo Vantage, HRCT, etc.) and should thus
be evaluated. Apart from on-line recording the software package
Para Graphics HRC should provide a heart-rate controlled training.
It should work automatically to control the speed of the treadmill
according to the desired range of the heart rate that should be
programmed. The following data should be recorded on-line:
Time [s]
Speed [km/h]
Heart rate [bpm]
Elevation [%]
Distance [km]
b) Rehabilitation attachment:- comfortable joint adjustment in width
and height ; with scale; the Reha attachment should be fixed to the
lateral railings of the Treadmill. the Reha attachment should be
folded together, and should not need to dismantle it after use
4. Full Resting ECG Evaluation 12 Leads with Computerized
Reporting Analysis of Waveform Morphology & Rhythm.
5. Computerized Treadmill Exercise Testing with 12 Leads, 3 leads
Screen Showing Advanced waveforms Analysis. Accurate ST
Segment Measurement, Heart Rate, BP Measurement should
include noninvasive BP measurement from time to time during
treadmill evaluations.
6. Facility for programmability for all variety of protocols.
7. Trend Charts for Heart Rate BP & ST shifts in at least 3 leads
available at the end of the test.
8. Minute to minute Evaluation of all leads available at the end of the
test.
9. 12 lead Printout to be available as & when necessary during the
test.
10. Stable Reusable Electrode that gives clear good quality online ECG.
11. ST Analysis of all 12 leads at maximum ST Depression & at
Maximum METs should be available at the end of the test.
12. Minute to minute evaluation of HR, BP, METs, Speed , Percentage of
elevation of Treadmill Belt, ST Analysis in minimum 3 selected
leads or maximum ST Depression out of all leads should be
available at the end of the test.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 All consumables required for installation and standardization of
system to be given free of cost.
5 Environmental factors
61
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10 -40 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Suitable Servo controlled Stabilizer/CVT
7 Standards, Safety and Training
7.1 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.2 10 years warranty on Driving Motor.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spares and accessories with their part number
and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
62
for ECG waveform, electrode impedance check, low battery/
lead fail display.
4. Should provide standard Full Interpretation of Supine ECG
with reasoning.
5. Display of real time 12 lead diagnostic quality ECG
waveform, average complexes beat of all 12 leads with
superimposed color comparison along with digital value of
ST level and slope. Display the graph on the recording
paper.
6. Automatic detection, display, Storage and review of
arrhythmia, Heart Rate, Double Product and METS. It
should have online HR METs and ST running trends
available on the screen during exercise.
7. System should have ability to manual edit of J & Isoelectric
point during exercise. Filters for line frequency and special
filters to reduce noise and baseline artifacts without
compromising the ECG frequency response.
8. System should have full disclosure play back, review and
storage of patient ECG raw data for unlimited numbers
depending upon size of the hard disk. The unit should have
the ability to readjust “J-ST” interval measurement + 1 m
sec points and generate a new report from stored raw ECG
data.
9. System should provide multiple and customizable printing
formats as per user’s choice on A-4 size high resolution
thermal printer for online real time printings. Compatible
laser printer for printing reports on plain paper also to be
supplied.
10. System must have ECG trigger output to interface with
external automatic devices.
11. Heavy Duty Treadmill (Imported): Noise free TREADMILL
with speed ranging from 0.5 to 20 kmph and grade of 0 –
22% with suitable servo stabilizer.
12. Automatic Stress test Non Invasive Blood Pressure Monitor,
compatible with the treadmill stress Test System for bi-
directional exchange of data between the monitor and
analyzer. Optional Pulse Oximetry (SpO2) integrated with
NIBP Module to be quoted separately.of enlarged complex
and facility of dynamic lead selection for maximum ST
changes.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 All consumables required for installation and standardization of
system to be given free of cost.
5 Environmental factors
None
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz
6.2 Suitable Servo controlled Stabilizer/CVT
63
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
64
Windows Versions; SVGA Monitor size 15”;Inkjet printer; Modem
56K;latest anti-virus SOLOMAN & NORTON. 87
3.3 Complete software and hardware to interface the system and
analyze the results of parameters recorded.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 All media and consumables for setting up and standardization
should be provided free of cost.
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Shall be certified to be meeting the safety standards IEC- 60601-2-
26 PART 2: Particular requirements for safety of EEG Systems.
7.3 Manufacturer should be ISO certified for quality standards.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.6 User list to be provided with performance certificate.
65
1.1 Sleep lab system is required to study the sleep disorders by
recording and analyzing the parameters like EEG, SPO2 ETC when
the patient is sleeping.
2 Operational Requirements
2.1 The sleep system is required with all the equipments and
computer with analysis software with printer
3 Technical Specifications
3.1 SPECIFICATIONS OF SLEEP SYSTEM
(1) Ambulatory polysomnography with 26 channels and upto 8
of these should be EEG , should be light and compact. The
basic unit should not be more than 500 gm. including
batteries.
(2) Should have latest touch screen for device configuration ,
impedance measurement and signal control.
(3) Following parameters should be recorded ;
(a) 8 AC signals for EEG,EOG,EMG,ECG and IC-EMG.
(b) flow by using a thermistor (nasal-oral) or using a
nasal cannula.
(c) Effort should be measured using piezoelectrical
sensors.
(d) Pulse frequency and oxygen sensor should be
measured with a finger clip attached to the interval
pulse oximeter.
(e) Snoring detected by a microphone.
(f) Body position (back,stomach,left,right) by means of
an integrated body position sensor in the
patients yoke box.
(g) Estimation of sleep and wake phases should be
measured using accleration sensor attached to
patient wrist.
(h) Light sensor integrated in the base unit to measure
actual time in bed.
(i) NCPAP/BiPAP pressure and flow. 90
(j) Possibility for software to generate a sum of both
effort signals, and heart frequency generated from
ECG.
(k) Necessary signals (EEG, EOG.EMG) required for
sleep staging should be bundled into one cable/plug
harness.
(l) Sleep Stage Analysis should be based on criteria of R
& K. The average frequency value of the central EEG
lead should be calculated, sleep spindles, K-
complexes, REMs and movement arousals should be
detected and displayed.
(m) The displayed amount of sleep interruption within
specific time intervals should provide
information about the disorder of sleep architecture.
(4) Should have built – in pulse oximeter, display should be 120
x 64 pixel b/w , touch screen memory = PCMCIA or compact
66
flash card , 96 MB memory , optional 160 MB. Pulse
Oximeter – 75% - 100% Range
(5) 7 aux. Channels to connect to external sources like PH , et
CO2 , temperature , Oesophagus pressure , NPT etc.
(6) Software based on windows platform and after transferring
the data to PC , the data should be analyzed automatically
with a clear over view of the final result.
(7) Computer assisted analysis or even complete manual
evaluations should be possible. The analysis software
should also evaluate measurements of children and infants
taken specific aspects such as periodic breathing into
consideration.
(8) The yoke box incl. Integrated body position sensor should
not be more than 250 gms.
(9) Internal storage of raw data and automatic gain adjustment
for perfect amplification of the respiratory signals should
be possible.
(10) Computer specification :CPU Pentium Core 2 Duo 2.7 GHz
and above;512 MB RAM;1.44 MB Floppy drive;120 GB Hard
Disk Drive; High Speed DVD/CD Rom 52 X: Serial .USB and
parallel ports ;Keyboard (IOS) , Mouse and Mouse Pad;
Preloaded latest MS Windows Versions;LD/TFT SVGA
Monitor size 17”;Inkjet printer; Modem 56K;latest anti-
virus SOLOMAN & NORTON.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 All consumables required for installation and standardization of
system to be given free of cost.
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility. or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer should be ISO certified for quality standards.
7.3 Shall be certified to be meeting the safety standards IEC- 60601-2-
26 PART 2: Particular requirements for safety of EEG Systems.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
67
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
68
a) Helium Cylinder-01
b) Cylinders Diffusion Mixtures-02
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer should have ISO certification for quality standards.
7.3 Electrical safety conforms to standards for electrical safety IEC-
60601-1 General Requirements
7.4 Should comply with ATS/ ECCS Guidelines.
7.5 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
94
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spares and accessories with their part number
and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
69
2 Operational Requirements
2.1 Complete system is required along with control software, PC and a
printer.
3 Technical Specifications
3.1 SPECIFICATION FOR A COMPUTERISED PFT SYSTEM
1) The System should be an economically oriented lung
function measuring system for the determination of the
static and dynamic lung volumes using the classical FRC-
Helium rebreathing and the Diffusion Capacity by using the
single Breath technique. It should also be possible to
measure Diffusion Capacity (DLCO) by the Rebreathing
technique for patients with distribution impairments of the
lungs, to minimise patient co-operation. 2) The system
should measure the following:
a) Slow and forced spirometry (Inspiratory and
Expiratiory Flow Volume Curve)
b) Lung subvolumes - Functional residual Capacity
(FRC), Residual Volume (RV). Total Lung Capacity
(TLC) by FRC-Helium multiple breath technique.
c) Diffusion capacity of the lung, by single breath
technique.
d) Diffusion capacity of the lung by the multiple breath
technique.
3) The system should measure the following
parameters:
a) Slow and forced Spirometry, VT, BF, MV, ERV, FVC,
FEV1, VCin, VCex, MEF 50, MEF 75, PEF, MVV etc.
b) Lung Subvolumes : FRC, RV, TLC, RV%TLC etc.
c) Diffusion capacity of the Lungs : DLCO-SB , DLCO –
RB.
4) The system should have an easy to exchange, bidirectional heated
pneumotach with the following specifications. :
Range - Should be 0 to 20 lit/sec.
Accuracy - Should be +/-2%
Resistance - Should be less than 0.05 KPa/ lit/sec.
5) The system should have carbon monoxide analyser, He analyser
and O2 Analyser with the following specifications:
a) Carbon monoxide analyser : Range - Should be from 0 to
0.4% Resolution/Accuracy should be 0.0002%/0.0003%
Reproducibility should be 0.0006%
b) He Analyser : Range - Should be 0 to 9.5%
Resolution/Accuracy should 0.005% /0.05 %
Reproducibility should be 0.02%
c) O2 analyser Range - Should be 0 to 100%.
Resolution / Accuracy should be 0.05% / 1.0%
Reproducibility should be 0.1%.
6) The system should have a demand valve unit for direct breathing
(no inspiratory bag) from pre-mix gas container, to minimise
wastage of gas.
70
7) The computer system should have the following specification:
Branded - Pentium Core 2 Duo processer 2.7 GHz and above
120 GB HDD,512 MB RAM,1.44 MB FDD,DVD RD/WR
Serial / Parallel Ports/USB,15” TFT Monitor.Keyboard,Mouse.
HP colour inkjet printer
ORIGINAL WINDOWS XP PROFESSIONAL
OEM O.S.WITH SERVICE PACKS 2
8) System software should have facility for entry of patient data and
saving of this information in a data base system Software should
be MS-windows based . It should be possible to configure different
report out put formats.
9) It should be possible to upgrade the system to the following :
a) Airway resistance by shutter method.
b) Respiratory impedance by Impulse Oscillometry system.
c) Respiratory muscle strength, Respiratory drive.
d) Compliance - Static / Dynamic system.
e) Body Plethysmography.
f) Aerosol Provocation system.
g) Ergospirometry & Stress test ECG.
h) Breathing Analysis for children.
10) The system should have fully computerised calibration procedure
for flow sensor and gas analysers. The system should also have a
check procedure during start-up.
11) It should be possible to integrate/connect the system in a local
Area Network (LAN). The data base must be accessed in a novel
authorised operating system.
12) The software for diffusion must have program for patient training
of DLCO Test without gas.
13) The software must be able to be set values for discard volume,
Alveolar time & other parameters according to user requirement.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 Should be supplied complete with Computer Interfacing package,
cables, Trolley, PFT Software, Manual and standard accessories
4.3 Should be supplied complete with Gas mixture cylinders (at least 2
cubic metres)
a) Helium Cylinder-01
b) Cylinders Diffusion Mixtures-02
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
71
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer should be ISO certified for quality standards.
7.3 Electrical safety conforms to standards for electrical safety IEC-
60601 / IS- 13450
7.4 Should comply with ATS/ ECCS Guidelines.
7.5 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
72
18. Silencing feature for audio alarms
19. Trend display from 2 to 24 hours
20. RS232 serial data output provision (peripheral printer or network),
analogue output for ECG
21. Defibrillator sync and protection
22. Pacemaker detection/rejection
23. Display reports system errors, leads and sensors failure and built-in
battery status
24. Unit can be mounted on standard bed/wall rail or mobile pole/stand.
25. Automatic switch from mains to batteries in case of power failure
26. Monitor: constructed of durable shock proof plastic
27. Power requirements: 220 V / 50 Hz (with adapter) or internal re-
chargeable batteries (autonomy approx 3 hrs, automatic recharge)
1 28. Battery backup minimum 2 hrs.
73
0 10. Should have event summary facility for recording and printing at least
250 events and 50 waveforms.
1 11. Should have facility to store patient data in internal memory and on
data card typically more than 90 minutes of patient ECG &events.
9 12. Should have a battery capable of usage for at least 90minutes or 40
discharges.
10 13. Should be capable of printing Reports on Event summary,
configuration, self test, battery capacity etc.
11 14. Should have facility for self test/check before usage and set up function.
12 15. Should have SP02 and non invasive pacing facility.
13 16. Should be capable of delivering energy in increments of 1-2 joules up to
30J and increments of maximum 50J thereafter.
74
3 3. Automatic and manual printout mode
4 4. Internal memory for data storage
5 5. Splash-resistant alphanumeric keyboard and direct function keys
6 6. Reset zeroing, auto-base-line correction (0.5 Hz) and 1mV test
7 7. Electrode connection quality check
8 8. Filter setting for line-frequency (50 or 60 Hz) and tremor
9 9. Large back-lit LCD displays recorded data and failure announcements:
ECG- curves, leads, heart rate, patient name and ID, electrode control,
clock, leads, speed and filter setting
10 10. Integrated high-resolution 300 dpi thermal printer, width 210 mm
11 11. Print-out, folded thermo-reactive paper, format A4
12 12. Number of channels, selectable: 3, 6 or 12
13 13. Standard combination of channels or manually selectable
14 14. Paper speed, selectable: 5, 25 and 50 mm/sec
15 15. Sensitivity, automatic or selectable: 5, 10 and 20 mm/mV
16 16. Copy function
17 17. Built-in batteries and charging unit
18 18. When fully charged, the battery gives approx. 50 readings
19 19. Power requirements: 220 V / 50 Hz (with adapter) or internal re-
chargeable batteries (autonomy approx 6 hrs, automatic recharge)
20. Supplied with:
0 i. 1 x patient cable
1 ii. 6 x suction ball-type chest electrodes, reusable
2 iii. 4 x extremity clamp electrodes, reusable
3 iv. 1 x bottle of gel for electrodes
4 v. 1 x box of recording paper
5 vi. 1 x box ECG-electrodes (200 sets of 3 electrodes, chest and/or
extremities, diameter approx 22mm, ultra soft gel, self adhesive)
6 vii. 1 x spare set of fuses
75
7. Unit must be light weight and portable, with a battery back-up of
minimum 6 hours.
8. The system should supplied with following
i. System as specified- 01
1 ii. Reusable SPO2: Adult SPO2 sensor with cable- two nos. per monitor,
Paediatric and Neonate SPO2 sensors - one no. per monitor .
76
3. Auto cut off device for preventing entry of fluid in pump.
4. Fast and efficient jar change facility.
5. Easy access and control
6. It should be portable
7. Should be able to create desired maximum vacuum in- least possible time.
8. One plastic suction jar cover, steam sterilisable to be provided extra.
9. Two extra suction jars (Plastic) of capacity 1 and 1 liters should be quoted
with accessories like lid, tubing etc.
27. BI – PAP
1. Non invasive
2. Working in 5 modes (S/ST/PC/ Timed/ C – page, Av APS).
3. Bipap Spontaneous or Spontaneous / timed
77
EQUIPMENT LABORATARY-5
1. Blood Gas Auto Analizer
Bench top Blood Gas Analyser for use in critical care testing. Measured
parameters: pH, pCO2, pO2 , tHb, Oxygen Saturation - Na +, K+, Ca++, Cl- , Haematocrit
Additional Calculated Parameters: up to 30 Parameters. Maintenance-free
electrodes. Typically 70 micro liters of sample for up to 10 parameters. Sample
throughput: 30 samples per hour. Should accept whole blood and QC materials for
blood gas measurements. Should be able to generate Levy-Jennings plots from QC
measurements. Electrolytes should be measurable on whole blood, serum and
plasma, Dialysate solutions. Fully automatic liquid calibration for all parameters
using internally generated gases. No gas cylinders. .Economy mode should be
possible in automatic/manual modes. In-built data management package to store
patient results, QC results, calibration reports and self-diagnostics for up to two
months. Remote instrument control and HIS connectivity. Built-in graphic thermal
printer. Color touch screen. Bar code scanner for lab automation. Operating
conditions: Instrument: +15 deg C to +33 deg C Electrodes: +37 deg C Solutions: +15
deg C to +33 deg C Electrical Data: Mains voltage: 220 volts Frequency: 50 Hz
2. Provides calculated parameter FiO2, tHb, SO2%, p50, Standard Bicarb, HCo3
levels, Anionic gap, Hct,RI, Qt, VO2, DO2, BO2,
78
9. The price quoted should be inclusive of the cost of electrodes for minimum
period of 3 years. Should also provide sufficient sets of reagent / calibration and
flusing fluids or gas, free of cost in a span of one year or equivalent of 5000 tests.
10. Instrument should have well configured assembly of wet sections, tubing and
valve so that disconnection and breakage are minimized
12. The reagents on board should have minimum expiry period of 12 months
13 To be provide a device which will uniformly mix heparin and blood, quickly
remove air bubble and eliminate clot formation.
14. Instrument should be CE / FDA / EU certified and comply with all electrical and
instrument regulations applicable of similar Lab / Medical equipment
3. Spiro meter
windows based pulmonary function analysis system useful to conduct FVC, SVC,
MVV and broncho provocation challenge tests unique patients incentives for adult and
pediatric patients undergoing pulmonary tests to achieve maximum effort easily complete
system dedicated to provide a simple solution for evaluation of pulmonary functions Flow
meter method bi-directional digital turbine flow detection opto-electronic semiconductor
sensor volume range 14liter flow range 0.03- 20lts/sec flow accuracy +- 3% User
selectable predicted values ERS93,Knudson83, ITS white, ITS black, LAM, Barcelona,
Indian, user programmable Test method FVC, SVC, MVV tests conducted sequentially
optionally broncho challenges as per methacholine challenge protocols Database MSAccess
easy recall of any previous test Internet connectivity remote review dedicated BPL
arpimis software Upload methods test sent as emailattachments Physical characteristics
instrument dimensions 200mm x 150mmx80mm approximate instrument weight 250
grams standard accessories pneumotch 1no, serial cable with adapter 1no, software 1no,
pediatric adaptor 1nos, pediatric mouthpieces 15nos, adult mouthpieces 25nos, 25 to 9 pin
adapter 1nos 43a Suitable P.C. and Printer for above Spiro meter
79
6. Rechargeable battery capable of sealing more than 500 to 1000 seals, when
fully charged.
80
EQUIPMENT NEPHROLOGY-6
1. Equipment Specifications for Haemodialysis Machine
1 Description of Function
1.1 Haemodialysis is a method for removing waste products as well as
free water from the blood when the kidneys are incapable of this.
2 Operational Requirements
2.1 Machine should have facility for Acetate, Bicarbonate and
Sequential dialysis (Isolated UF).
2.2 Can be linked with Patient Data Management System and should
be upgradable to future software developments
2.3 The blood pump should run even in the absence of water or
dialysate flow.
3 Technical Specifications
3.1 Should have facility for conventional and High flux dialysis.
3.2 Deleted
3.3 Deleted
3.4 Machine should have two bacterial filter (Pyrogen filters) one at
water inlet and one before water going to dialyser
3.5 Battery back-up for at least 30 minutes to run complete machine
with heater supply
3.6 Should have Na, Bicarbonate and UF profiling
3.7 Dialysate temperatures selectable between 35 degrees C to 39 deg.
C
3.8 Variable conductivity setting between 12 to 15
3.9 Should have variable dialysate flow 250-800 ml/mt
3.10 Should have facility to show trends curve of all parameter for 15-
20 minutes
3.11 Heparin pump with syringe sizes up to 50 ml with pump flow rate
from 1-10 ml/hr( 0.1 ml increments)
3.12 Stroke pressure operated short term single needle dialysis
(Optional)
3.13 Ultrafiltration 0.1 to 2.5 litres/hr.The in and out fluid circuit must
be separated so that there is no chance of contamination in the
event of membrane rupture.
3.14 Treatment parameter should be displayed by graph and digitally
both
3.15 Should have integrated heat (800C) and chemical disinfection
facility.
3.16 Should have accurate feedback control conductivity mixing
technique.
3.17 Should have drain facility.
3.18 Should have accurate UF control by flow measurement technique.
3.19 Extra facilities like Blood Volume sensor, Bicart Select technique
and online clearance kt/V (Optional)
3.20 All important data should be preset so that machine can be used
anytime without feeding data every time
3.21 Should have automatic self test facility
3.22 Should have auto ON/OFF Facility
81
3.23 Should have touch button screen
3.24 Easy to service, troubleshoot and calibrate
3.25 Machine can be connected to computer to feed all data and trouble
shoot whenever any problem
3.26 Blood pump rate from 20-500 ml/min adaptable to all standard A-
V blood lines
3.27 Ability to monitor pulse rate and NIBP with graphic and tabulated
trends.
3.28 Audio visual alarms on limit violation of conductivity, blood leak,
air leak, transmembrane pressure alarms,, Dialysis temperature
alarm, dialysis can empty alarm, end of disinfection alarm, bypass
alarm and blood pump stop alarm
3.29 Alarm for reverse Ultra filtration.
4 System Configuration Accessories, spares and consumables
4.1 System as specified-
4.2 All consumables required for installation and standardization of
system to be given free of cost.
4.3 To be supplied free of cost
Bacterial filters– 2 sets extra , 100 polysulfone 1 m2 dialyzers and
tubings
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Shall comply with IEC 60601-2-16 SAFETY requirements of
medical electric equipment part2- particular requirements for the
safety of Haemodialysis equipment.
7.4 Comprehensive warranty for 5 years and 5 years AMC after
warranty supported by the principal manufacturers.
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
7.6 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
82
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. As per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instruction for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital
technician and company service engineer should be clearly spelt
out
83
3.18 Three weighing scales to control system with balancing accuracy
of less than 1% of total turnover in normal conditions and
weighing capacity of at least 0-20kg.
3.19 Integrated Fluid/Blood warmer for blood/dialysate warming temp
range app 33-40 deg C(+/- 3 deg C)
3.20 Ultrasonic air bubble detector and Blood leak Detector.
3.21 Alarm in case of blood leak, air in line, pressure limit violation,
empty dialysate/ replacement bag, full effluent bag and advisory
alarms in case of excessive TMP and filter clotting.
3.22 Should have a 30 mt Battery back up including Heater and pumps.
3.23 Should have an RS 232 Port for Data transfer and interface.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 The system should be compatible with Universal Heamodialysis/
Haemofiltartion
4.3 Should be supplied with 250 Nos of essential accessories such as
blood line set, haemofilters and ultrafiltrate bags at no extra cost.
4.4 All media and consumables for setting up and standardization
should be provided free of cost in addition to the items supplied in
4.3.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0-50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Comprehensive warranty for 5 years and 5 years AMC after
warranty supported by the principal manufacturers.
7.4 Shall comply with IEC 60601-2-16 SAFETY requirements of
medical electric equipment part2- particular requirements for the
safety of Haemodialysis equipment.
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
7.6 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
84
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
85
4.1 System as specified-
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility.or
should comply with 89/366/EEC;EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Electrical safety conforms to standards for electrical safety IEC-
60601 / IS18 13450
7.4 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual
7.5 Comprehensive warranty for 5 years and 5 years AMC after
warranty supported by the principal manufacturers.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of important spare parts and accessories with their part
number and costing.
8.4 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.5 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
86
3.3 Should have an option for manual operation of all controls
3.4 Armrest should fold to allow side entry of the patient.
3.5 Head rest should be detachable and should have manual
Trendelenburg facility.
3.6 Seat cushion should be removable, made of proper density foam
and should have a smooth surface for easy hygiene and cleaning.
3.7 Frame should be made up of corrosion free galvanized steel with
powder coating and should have four 150mm dia swiveling castor
wheels of which the front two should be lockable
3.8 Should be able to withstand a maximum load of 150 Kg.
3.9 Should have facility for online weight measurement (optional).
3.10 Dimensions(approx 5 cm): Width 63 cm x Length 195 cm( fully
stretched)x Adjustable Height( Min 56 cm; Max 78 cm from
ground)
3.11 Rubber buffers are to be provided
3.12 Should have a detachable drip stand and a tray table.
4 System Configuration Accessories, spares and consumables
4.1 System as specified-
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI
Specifications.( Input 160-260 V and output 220-240 V and 50 Hz)
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufactures/Supplier should have ISO certificate to Quality
Standard.
7.3 Comprehensive warranty for 2 years and 5 years AMC after
warranty supported by the principal manufacturers.
7.4 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
7.5 All electrical actuators and mechanisms should be housed inside
the structure making the product safer
7.6 Electrical safety conforms to standards for electrical safety IEC-
60601 / IS- 13450
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of important spare parts and accessories with their part
number and costing
8.4 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
87
hospital technician and company service engineer should be
clearly spelt out.
8.5 User list to be provided with performance certificate.
8.6 List of Equipments available for providing calibration and routine
Preventive Maintenance Support as per manufacturer
documentation in service/technical manual.
88
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Comprehensive warranty for 5 years and 5 years AMC after
warranty supported by the principal manufacturers.
7.4 Comprehensive training for lab staff and support services till
familiarity with the system.
7.5 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing
8.5 Log book with instruction for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital
technician and company service engineer should be clearly spelt
out
8.6 User list to be provided with performance certificate.
89
3.4 The entire unit should have adequate monitoring of input and
output water conductivity, feed water pressure and rejection flow
rate.
3.5 The system should have protection alarm against low feed water,
high output conductivity and high temperature of pump motor.
3.6 The system should include online water distribution to 15-20
machines in loop so that the unused water may be fed back to
treatment unit, thus saving on water rejection.
3.7 The unit should have programmable and automatic
rinsing/flushing facility, at regular intervals, when system is not in
use, to prevent drying of filter media and R.O. Membrane.
3.8 The system should have programmable disinfection /de-
calcification facility using commonly available disinfection /
decalcification chemicals.
3.9 The system should accept feed water with TDS upto 1500 mg/litre
and hardness up to 1 dH with 0.5% rejection of TDS & hardness
and 99% rejection of bacteria and endotoxins.
3.10 The unit should be designed for maximum saving of raw water,
with efficiency of 60-70%.
3.11 The water distribution loop, booster pump and storage water tank
should be made up of stainless steel. Storage water tank should
have capacity of at least 5000 litres with water level controller,
outlet valves and easy cleaning provisions.
4 System Configuration Accessories, spares and consumables
4.1 System as specified-
4.2 The vendor should provide a system on a turnkey basis including
all civil and electrical works including two booster pumps in
parallel for providing water delivery. The vendor should inspect
the site for this purpose.
4.3 The vendor should supply adequate filter cartridges, media or
resins to last for at least 3 years. The vendor may visit the site and
check the water quality.
4.4 The vendor should provide preventive maintenance which
includes chemical checks, bacterial and pyrogen checks
periodically during the warranty period.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 -40deg C and relative humidity of 15-90%
5.3 The hospital will provide vacant space, water outlets and electrical
points as specified by the vendor. Other plumbing works and civil
works will have to be undertaken by the bidder. Vendor should
ensure that there is no environmental damage of any kind takes
place.
6 Power Supply
6.1 Power input :220-240V/ 50 Hz AC Single phase or 380-400V AC 50
Hz Three phase fitted with appropriate Indian plugs and sockets.
7 Standards, Safety and Training
90
7.1 Output water quality should match AAMI(Association for the
Advancement of Medical Instrumentation) standards for
Haemodialysis Water( Al < 0.01 mg/L; Ca < 2 mg/L; BACTERIA<
200 CFU/ml)
7.2 Should be FDA , CE,UL or BIS approved product
7.3 Manufacturer/Supplier should have ISO certification for quality
standards.
7.4 Comprehensive warranty for 5 years and 5 years AMC after
warranty supported by the principal manufacturers.
7.5 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.6 User list to be provided with performance certificate.
91
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient
temperature of 10-40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Normal Power 220-240 Volts AC 50 Hz with a suitable adopter or
Battery Rechargeable
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Electrical safety conforms to standards for electrical safety IEC-
60601-1 General Requirements
7.4 Comprehensive warranty for 5 years and 5 years AMC after
warranty supported by the principal manufacturers.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of important spare parts and accessories with their part
number and costing
8.4 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.5 List of Equipments available for providing calibration and routine
maintenance support as per manufacturer documentation in
service / technical manual
92
EQUIPMENT UROLOGY-7
1. Equipment Specifications for Urodynamic System 6 Channel
(HIGH END)
1 Description of Function
1.1 The Urodynamic system should have a 6 channel microprocessor
based compact system with a high resolution color monitor for the
Urodynamic study for Neurovesical and erectile dysfunction The
equipment should be modular design and should be able to
carryout different tests like Uroflowmetry, Cystometry (CO2 &
H2O), Electromyography (EMG), Urethral pressure profile (UPP),
Pressure flow study (PFS), Video Urodynamics, Bladder/Valsalva
leak point measurement & Cavernosometry.
2 Operational Requirements
2.1 The equipment should be modular design and should be able to
carryout different tests like Uroflowmetry, Cystometry (CO2 &
H2O), Electromyography (EMG), Urethral pressure profile (UPP),
Pressure flow study (PFS), Video Urodynamics, Bladder/Valsalva
leak point measurement
3 Technical Specifications
3.1 The pre set program should be done on the screen according to
selected tests
3.2 There should be online monitoring of measurement up to six
parameters with simultaneous measurement of three direct
pressure studies like vesical, abdominal and urethral
3.3 There should be a high resolution, medical grade 17” TFT monitor
with speaker & microphone with a dedicated controlled keyboard,
mouse, speakers for EMG
3.4 Facility for fully automatic comprehensive patient filing & report
generation with editing/post processing mode. Appropriate
software for analysis of data including p-q Plot & Stress profile.
3.5 The pressure transducers should be of long life Statham
transducer so as to last for more than 8-10 years The
Uroflowmetry should have rotating disc transducer or weight
transducer so as to provide graphical representation of relation
between detrusor pressure and uro-flow rate
3.6 The equipment should have control panel inside the equipment to
avoid water spillage.
3.7 Advanced window based Software for operating, analyzing &
report generation with templates of full text.
3.8 Flowmetry : Range – 0-60ml/sec; Volume – 2 l Transducer –
Rotating disc type/weight transducer
3.9 Pressure Study : Range: 1 – 250 cm of water; Transducer – Long
life Statham type
3.10 EMG : One channel with inbuilt speaker & voice annotation, low
frequency
3.11 Water Pump Unit : Infusion Rate – 2-10ml/min, Increment –
1ml/min –10-100ml/min, Increment – 5ml/min
93
3.12 Console : Pentium Duo Core 2.5 GHz or more with a hard disk
drive (HDD) –120GB & RAM-512MB, DVD-writer 18X or more for
recording of DVDs/CDs
3.13 Equipment should have Uro-Video system with facility to super-
impose the bladder images on graph tracing and PIP with graph
tracing. Facility for Digital video recording
3.14 Patient Unit should include :Trolley –1, Pole – 1, 17” Monitor
with speakers & microphone-1, Water Pump Unit with 30 infusion
sets, EMG Module-1, Pressure Transducer Statham-3,
Uroflowmetry transducer-1, Puller for urethral pressure profile
study.
3.15 Software in Original: Windows XP, Office XP - Latest &
compatible
3.16 Facility to connect with hospital information system (HIS - VII) and
to transfer data through cable.
3.17 Suitable Micturition chair - separate
3.18 The Urodynamic system should be up gradable for future with
technical advances
3.19 Suitable Laser Printer.
3.20 Suitable C – Arm with 9” IITV and diagnostic Ultrasound system to
be integrated with the Urodynamic system.
4 System Configuration Accessories, spares and consumables
4.1 System as specified-
4.2 All consumables required for installation and standardization of
system to be given free of cost as mentioned below:
Dampening tube-24, Two lumen catheter-12, Infusion set-12, Y-
Piece-4, Three way stop cork-50, Disposable Domes-50, Rectal
catheter-4, , Concentric needle electrode-10, Ground Electrode-4,
Surface Electrode-12, Pressure line (150cm) – 50, Anal plug
electrode – 2
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Shall comply with IEC 60601-2-16 SAFETY requirements of
medical electric equipment part2- particular requirements for the
safety of Haemodialysis equipment.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
8 Documentation
94
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer documentation in
service/technical manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily , weekly, monthly and quarterly
maintenance checklist.
The job description of the hospital technician and company service
engineer should be clearly spelt out
95
3.6 The equipment should have control panel inside the equipment to
avoid water spillage.
3.7 Advanced window based Software for operating, analyzing &
report generation with templates of full text.
3.8 Flowmetry : Range – 0-60ml/sec; Volume – 2 l Transducer –
Rotating disc type/weight transducer
3.9 Pressure Study : Range: 1 – 250 cm of water; Transducer – Long
life Statham type
3.10 EMG : One channel with inbuilt speaker & voice annotation, low
frequency
3.11 Water Pump Unit : Infusion Rate – 2-10ml/min, Increment –
1ml/min–10 100ml/min, Increment – 5ml/min
3.12 Console : Pentium Duo Core 2.5 GHz or more with a hard disk
drive (HDD) –120GB & RAM-512MB, DVD-writer 18X or more for
recording of DVDs/CDs
3.13 Equipment should have Uro-Video system with facility to super-
impose the bladder images on graph tracing and PIP with graph
tracing. Facility for Digital video recording
3.14 Patient Unit should include :
Trolley –1, Pole – 1, 17” Monitor with speakers & microphone-1,
Water Pump Unit with 30 infusion sets, EMG Module-1, Pressure
Transducer Statham-3, Uroflowmetry transducer-1, Puller for
urethral pressure profile study.
3.15 Software in Original: Windows XP, Office XP - Latest &
compatible
3.16 Facility to connect with hospital information system (HIS - VII) and
to transfer data through cable.
3.17 Suitable Micturition chair - separate
3.18 The Urodynamic system should be up gradable for future with
technical advances
3.19 Suitable Laser Printer.
4 System Configuration Accessories, spares and consumables
4.1 System as specified-
4.2 All consumables required for installation and standardization of
system to be given free of cost as mentioned below:
Dampening tube-24, Two lumen catheter-12, Infusion set-12, Y-
Piece-4, Three way stop cork-50, Disposable Domes-50, Rectal
catheter-4, Concentric needle electrode-10, Ground Electrode-4,
Surface Electrode-12, Pressure line (150cm) –50, Anal plug
electrode – 2
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
96
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Shall comply with IEC 60601-2-16 SAFETY requirements of
medical electric equipment part2- particular requirements for the
safety of Haemodialysis equipment.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instruction for daily , weekly, monthly and quarterly
maintenance checklist. The job description of the hospital
technician and company service engineer should be clearly spelt
out
97
3.7 Auto diagnosis on switching on and during working to
continuously monitor all
3.8 Automatic stoppage of output in case of malfunction with acoustic
and visual signal with display of error code.
3.9 Output powers adjustable automatically or manually by membrane
keys or push buttons
3.10 Four or more programmable memory for output settings
3.11 Simultaneous access to mono and bipolar by 2 or more users
3.12 Should be usable with laparoscopic mono polar and bipolar
instruments
3.13 System for neutral plate safety by continuous monitoring of
contact quality and connection
3.14 System for monitoring and control of leakage current
3.15 Frequency leakage on the patient should be less than 10 micro
Amp.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 The accessories should include portable trolley, mains cable, foot
switches for mono and bipolar, reusable and single use neutral
electrode for adults and children, cable for neutral electrode, fixing
belt for neutral electrode (paed/adult),securing buttons for fixing
belt, sterilisable and or disposable electrode handle with and
without finger switch, cable for electrode handle, set of electrodes
(long and short), electrode container with holder, tip cleaner,
bipolar forceps, cable for bipolar forceps, cable for connecting to
mono polar laparoscopic instruments
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility or
should comply with 89/366/EEC; EMCdirective.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI
Specifications. (Input 160-260 V and output 220-240 V and 50 Hz)
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Certified to be compliant with IEC 60601-2-2 Medical Electrical
Equipment Part 2-2: Particular requirements for the safety of High
Frequency Surgical Equipments
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
7.6 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
98
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
99
• Colour temperature should be > 6000 K.
• Should have bulb life indicator. Bulb life should be
guaranteed for a minimum of 500 hrs 3.4 Light Cable:
• Fiber optic light cable autoclavable
• Length 350cm
• Diameter should be 4.8mm
3.5 Digital video recording, editing, image management and archival
system.
3.6 Nephroscopes:
i) For Adult Set (Standard and long length): Wide angle
straightforward telescope(s) 6 degrees with parallel
eyepiece, autoclavable, with leur lock connection, with
instrument channel. Fibre light transmission incorporated.
Light post adapter for Storz, Olympus and Wolf light cables.
ii) For Adult Set (Miniperc): Wide angle straightforward
telescope 6 degrees with parallel eyepiece, autoclavable,
with leur lock connection, with instrument channel. Fibre
light transmission incorporated. Light post adapter for
Storz, Olympus and Wolf light cables.
iii) For Paediatric set: Wide angle straightforward telescope 6
degrees with offset eyepiece compatible with 17/18Fr
Sheath, autoclavable, with leur lock connection, with
instrument channel. Fibre light transmission incorporated.
Light post adapter for Storz, Olympus and Wolf light cables.
3.7 Metallic Telescoping Dilation set, set of 8 dilators, sizes
9,12,15,18,21, 24,27 & 30 Fr, along with one rigid and one flexible
guide rod.
3.8 Metallic Alken dilator and cannula - One set
3.9 Operating Sheaths:
a) 26Fr Adult Sheath(s) with obturator (short and long) with
continuous irrigation and suction
b) Miniperc Sheath 17/22 Fr
c) 17/18Fr paediatric Sheath compatible with the above
nephroscope
3.10 Grasping forceps, alligator jaws & spring handle – Two numbers
3.11 Grasping forceps, 3 expanding jaws and small fixation spikes with
spring handle - Two numbers.
3.12 Biopsy forceps, double action jaws
3.13 Suction tube
3.14 Appropriate rigid storage case.
4 System Configuration Accessories, spares and consumables
4.1 System as specified along with compatible accessories as specified
from 3.10 to 3.14 for Adult, Miniperc and Paediatrics.
4.2 All consumables required for installation and standardization of
system to be given free of cost.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50 deg C and relative humidity of 15-90%
6 Power Supply
100
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 30 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufactures/Supplier should have ISO certificate to Quality
Standard.
7.3 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.4 Electrical safety conforms to standards for electrical safety IEC-
60601 / IS- 13450
7.5 Should have local service facility .The service provider should have
the necessary equipments recommended by the manufacturer to
carry out preventive maintenance test as per guidelines provided
in the service/maintenance manual.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job descriptin of the hospital
technician and company service engineer should be clearly spelt
out.
101
3.2 Imaging System: Integrated non detachable Fluoroscopy Should
have high frequency generator and allow pulse fluoroscopy. kV
Range: 40-110 kV mA Range: 4 – 8 mA Focal Spot Sizes: Dual:
0.3/0.6 and 0.6/1.2/1.5 Image Intensifier Size: 9 inches.
Collimation: Motorized, Iris collimator. Post Exposure Image
Enhancement facility. Imaging System Ultrasound: High resolution
ultrasound system Localization should be done through integrated
Ultra-sound iso centric to the shock wave source with
inline/outline transducer for best image quality
Transducer:
I) 3.5 /5 MHz Convex Sector
II) Ultrasound system should be able to accept 6.0-7.5 MHz
electronic biplane trans rectal probe. Mode: B Coupling arm
to integrate the ultrasound probe with shockwave
generator.
3.4 Patient Table System:
i) Fluoroscopy compatible, motorized patient Table with
Vertical, Longitudinal and lateral movements. Facility for
tilt and trendelenburg. Patient load capacity of app 150 Kg.
ii) The table should be provided with accessories suitable for
urological endoscopic procedures
3.5 Flouroscopic Imaging System: 17 inches LCD Display with data
storage and image storage. Minimum storage would be 1000
images with 1024x1024x(12 bits)
3.6 Patient Monitoring: Monitoring of ECG, RESPIRATION, SpO2 and
Arrhythmia.
3.7 Separate Remote Console with facility for:
i) Controlling imaging, computerized stone localization,
targeting and shockwave parameters
ii) Patient monitoring
4 System Configuration Accessories, spares and consumables
4.1 System as specified
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0-50 deg C and relative humidity of 15-90%
5.3 Pre Requsites should be clearly spelt out in terms of room
requirements, civil and electrical works.
6 Power Supply
6.1 Power input: 220-240V/ 50 Hz AC Single phase or 380-400V AC 50
Hz Three phase fitted with appropriate Indian plugs and sockets.
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI
Specifications. (Input 160-260 V and output 220-240 V and 50 Hz)
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
7.2 Should be compliant to ISO 13485: Quality systems - Medical
devices – Particular requirements for the application of ISO 9001
102
applicable to manufacturers and service providers that perform
their own design activities.
7.3 Electrical safety conforms to standards for electrical safety IEC-
60601-1 General Requirements
7.4 Comprehensive warranty for 5 years and provision of AMC for
next 5 years.
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support as per manufacturer
documentation in service/technical manual.
8.4 List of important spares and accessories with their part number
and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.6 Must submit user list and performance report within last 5 years
from major hospitals.
103
Localization should be done through integrated Ultra-sound iso
centric to the shock wave source with inline/outline transducer for
best image quality
Transducer:
I) 3.5 /5 MHz Convex Sector
II) Ultrasound system should be able to accept 6.0-7.5 MHz
electronic biplane trans rectal probe.
Mode: B Coupling arm to integrate the ultrasound probe
with shockwave generator.
3.4 Patient Table System:
i) Fluoroscopy compatible, motorized patient Table with
Vertical, Longitudinal and lateral movements. Facility for
tilt and trendelenburg. Patient load capacity of app 150 Kg.
ii) The table should be provided with accessories suitable for
urological endoscopic procedures
3.5 Flouroscopic Imaging System: 17 inches LCD Display with data
storage and image storage. Minimum storage would be 1000
images with 1024x1024x(12 bits)
3.6 Patient Monitoring: Monitoring of ECG, RESPIRATION, SpO2 and
Arrhythmia.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
5 Environmental factors
5.1 Shall meet IEC-60601-1-2:2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility or
should comply with 89/366/EEC; EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0-50deg C and relative humidity of 15-90%
5.3 Pre Requsites should be clearly spelt out in terms of room
requirements, civil and electrical works.
6 Power Supply
6.1 Power input: 220-240V/ 50 Hz AC Single phase or 380-400V AC 50
Hz Three phase fitted with appropriate Indian plugs and sockets.
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI
Specifications. (Input 160-260 V and output 220-240 V and 50 Hz)
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
7.2 Should be compliant to ISO 13485: Quality systems - Medical
devices – Particular requirements for the application of ISO 9001
applicable to manufacturers and service providers that perform
their own design activities.
7.3 Electrical safety conforms to standards for electrical safety IEC-
60601-1 General Requirements
7.4 Comprehensive warranty for 5 years and provision of AMC for
next 5 years.
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
104
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support as per manufacturer
documentation in service/technical manual.
8.4 List of important spares and accessories with their part number
and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
8.6 Must submit user list and performance report within last 5 years
from major hospitals.
105
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 30 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Shall comply with IEC 60601-2-16 SAFETY requirements of
medical electric equipment part2- particular requirements for the
safety of Haemodialysis equipment.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Comprehensive training for lab / OT staff and support services till
familiarity with the system.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instruction for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital
technician and company service engineer should be clearly spelt
out
106
3.1 Length: 37 cm (approx) Direction Of View: Straight forward (zero
to six degrees). Working Channel: 6.0 Fr or better Distal tip
Diameter: 14.0 Fr (approx) Tip deflection: 140 degree (down) –
210 degree (up) Angle of view: About 110 degrees
3.2 Compatible Accessories
(viii) Grasping forceps – 2 Nos.
(ix) Biopsy forceps – 2 Nos.
(x) Ball tip Fulgurating electrode 5 Fr – 2 Nos.
(xi) Luer Lock Y connector Biopsy port
(xii) Soak disinfection tray
(xiii) Cleaning brush – 2 Nos.
(xiv) Appropriate rigid storage case
4 System Configuration Accessories, spares and consumables
4.1 System as specified-
4.2 All consumables required for installation and standardization of
system to be given free of cost.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 -50deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 30 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA, CE, UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Shall comply with IEC 60601-2-16 SAFETY requirements of
medical electric equipment part2- particular requirements for the
safety of Haemodialysis equipment.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Comprehensive training for lab / OT staff and support services till
familiarity with the system.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instruction for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital
technician and company service engineer should be clearly spelt
out
107
9. Equipment Specifications for O.T. Table for Urology
1 Description of Function
1.1 A dedicated system for Urological surgery (Endoscopic as well as
open surgeries).
2 Operational Requirements
2.1 Multi purpose powered OT table, C- Arm Fluoroscopic compatible,
suitable for all major surgical procedures, complete with a corded
handset with battery level indicators (choice of IR handset should
also be available) and moulded, anti-static, seamless mattress.
3 Technical Specifications
3.1 Table should feature of sliding table top with a traverse of
minimum of 250mm or more, either Cranially or Caudally
3.2 Full length X-ray translucent top with removable &
interchangeable head and leg sections with an auto-locking
mechanism.
3.3 Table must allow for unrivalled C-arm access and kidney break
positioning without the need to move the patient.
3.4 The handset should offer controls for trendelenberg / reverse
trendelenberg, lateral tilt, flexion/extension (90/230 degree),
longitudinal tabletop traverse and height functions (min. height
around 700-800mm and max. height around 1000- 1200mm).
3.5 The brakes, wheels and castors should be controlled by two foot
pedals provided at either end of the table
3.6 The table should feature an integrated stand by panel for
controlling the movements in case of handset loss or battery
failure
3.7 The Table stem should be located under the middle of the back
section making the tabletop eccentric.
3.8 Table should be able to carry heavy patients and have a capacity of
up to 300kgs with an option for width extension of obese patients.
3.9 Table should also be suitable for tall patients and have a length of
at least 2000 mm
3.10 Table should offer low minimum height enabling the surgeon to
operate even when seated
3.11 The table should have divided leg section with mattresses, arm
board & universal clamp
3.12 Should have facilities for manual operations in case of power
failures.
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 The table should be supplied with following necessary accessories
including knee crutches:
a. Arm supports – 2
b. Gel heel pads – 1 pair
c. Patient positioning gel strap, 200-250cms – 1
d. Hand Surgery Board – 1
e. Anaesthetic screen with sleeve – 1
f. Lithotomy Poles/crutches with pads – 1 pair
g. Douche tray with strainer to be fixed with table – 1
108
h. Elevated Arm Support - 1
i. Freddicks Lloyd Davis Stirrups – 1 pair
j. Fluoroscopic compatible Kidney Bridges
k. Padded head, shoulder and arm rest – 1 set each
l. Padded lateral support and shoulder supports – 1 set
m. Appropriate accessories’ clamp.
4.3 Table should be quoted with Suitable Chair for the surgeon for
endoscopic procedures,1
5 Environmental factors
5.1 Shall meet IEC-60601-1-2: 2001(Or Equivalent BIS) General
Requirements of Safety for Electromagnetic Compatibility or
should comply with 89/366/EEC; EMCdirective.
5.2 The unit shall be capable of being stored continuously in ambient
temperature of 0-50deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI
Specifications.(Input 160-260 V and output 220-240 V and 50 Hz)
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Should have current leakage less than 70 U/A AC (0.07m Amp).
7.3 Manufacturer/Supplier should have ISO certification for quality
standards.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instructions for daily, weekly, monthly and
quarterly maintenance checklist. The job description of the
hospital technician and company service engineer should be
clearly spelt out.
109
Autoclavable with offset Eyepiece, Distal sheath tip 7.5 – 8 FR, 5-8
degree with working channel of 5 – 6FR. Irrigation channel and
accessory Instruments including double instrument port with 425
mm working length. -Grasping forceps 5FR with working length
550 mm – 2 Nos. -Biopsy forceps 5FR with working length 550 mm
-Path finder plus bulb irrigator
3.2 Long Arm (Length ~ 420mm) Autoclavable with offset Eyepiece,
Distal sheath tip 6 – 6.5 FR, 5-8 degree with working channel of
4FR. Accessory Instruments including irrigation channel and
instrument port. -Appropriate Grasping forceps. – 2 Nos.
-Appropriate Biopsy forceps – 1No. -Path finder plus bulb irrigator
3.3 Short Arm (Length ~ 320mm) Autoclavable with offset Eyepiece,
Distal sheath tip 6 – 6.5 FR, 5-8 degree with working channel of
4FR. Accessory Instruments including irrigation channel and
instrument port. -Appropriate Grasping forceps. – 2 Nos.
-Appropriate Biopsy forceps – 1No. -Path finder plus bulb irrigator
`stem Configuration Accessories, spares and consumables
4.1 System as specified- along with light post adaptor for STORZ/
Olympus/ Wolf light cable
4.2 All consumables required for installation and standardization of
system to be given free of cost.
4.3 Appropriate Rigid Storage Box.
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient
temperature of 0 - 50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient
temperature of 10 - 40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection
for 60 minutes back up.
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality
standards.
7.3 Shall comply with IEC 60601-2-16 SAFETY requirements of
medical electric equipment part2- particular requirements for the
safety of Haemodialysis equipment.
7.4 Comprehensive warranty for 2 years and 5 years AMC after
warranty
7.5 Comprehensive training for lab staff and support services till
familiarity with the system.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine
Preventive Maintenance Support. as per manufacturer
documentation in service/technical manual.
110
8.4 List of important spare parts and accessories with their part
number and costing.
8.5 Log book with instruction for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital
technician and company service engineer should be clearly spelt
out
111
EQUIPMENT OPHTHALMOLOGY N ENT- 8
1. Slit Lamp Biomicroscope
TECHNICAL SPECIFICATION
1. Main Microscope Galilean, 5 Steps Magnification
2. Eye pieces 12.5x
3. Diopter Adjustment From + 6 to -6
4. Interpupilary Distance Adjustable from 55mm-75mm
5. Working Distance 100mm
6. Magnification Mannual 5 Step 6x, 10x, 16x, 25x, 40x
7. Field of View (in mm) 35, 23, 14, 8, 7, 5, 6
8. Slit Width 0 to14 mm
9. Slit length 0 to 14 mm
10. Slit Appertures 0.2, 1.3, 4.6, 10,14mm/
11. Slit Angles 0-180 deg.
12. Slit inclination 5,10,15,20 Deg
13. Filter Heat Absorbing Filter and UV, GREEN and BLUE Filters
14. Light source 12V/30W,Halogen
15. Movement Ranges :
0 i. Longitutional in/out 118mm
1 ii. Lateral (left/Right) 99mm
2 iii. Vertival (Up/Down) 30mm
3 iv. Chinrest Range 55mm
16. Voltage 220-240V,50/60Hz.
2. Photoslit Lamp
Imaging and Documentation System :
It should have the following features and facilities :
1 1) Live on screen view
0 2) Should come with Sony Firewire camera for still and movie capture
documentation software
2 3) Comprehensive Database with search and querry functions.
3 4) Unique patient identification.
4 5) User definable database.
5 6) Single and 4 –up image display.
6 7) Automatic archiving.
7 8) System Administration with password protection..
8 9) Import & export functions.
9 10) Image copy to email
10 11) User definable image compression
11 12) Brightness, contrast and gamma control
12 13) Image Zoom and resize
13 14) Red – Free, Negative, Green filter
14 15) Rotate & Invert image
15 16) Sharpening and Box Enhancement
16 17) Patient and Image Notes
17 18) Image annotation
18 19) Grading and Reporting
112
19 20) Multiple Print format and contact sheey print
20 21) Crash protection
21 22) Stereo image viewing
22 23) On-line help
23 24) It should have the facility of DICOM export.
24 25) Compatible PC should be provided
Slit lamp with specifications
1) Should have illumination from top using tungsten filament bulb capable of
giving illumination intensity up to 600,000Lux.
2) Magnification from 6.3X to 40X in 5 steps having steps at 6.3, 10,16, 25
and 40X.
3) Diameter of field should be from 32 mm to 5.1mm.
4) Slit length 0.2 to 8mm
5) Eyepieces of 12.5X.
6) Facility to tilt the slit image up to 20deg should be available.
7) Should have the facility for stereoscopic examination of fundus where in
Angle on stereoscopic observation can be reduced from 13deg to 4.5deg
to have better view of eyes with small pupil or high myopia.
8) Adaptor for Inclined Eye- piece to enable the viewing into the microscope
is inclined at 20° to the horizontal – thus enabling the examiner to keep
his head in a fatigue free position.
9) Should have the facility to attach beam splitter and adaptor for digital
camera.
10) Imaging with this slit lamp should be flash free.
11) Should have the facility of background illumination through a cold light
source.
12) Original Goldman Applanation tonometer
13) Spring balanced table for slit lamp.
113
4. Indirect Ophthalmoscope
1 1. Weight of Head band with Light weight 500-600 gm with soft
cushioning and non slip contoured ophthalmoscope metallic head
band.
2 2. Bulb 6V with easy fit, push in (halogen bulb)
3 3. Illumination 2000lux, rheostat-On head band & Illumination should be
adjustable from 100% to 2% of max required
4 4. Diffuser Should have both wireless and must run for100min with
battery rechargeable on lithium batteries with 2 extra batteries with
charger
5 5. Transformer runs with wide angle run.
6 6. Filters 4
0 a. Diffuse,
1 b. Yellow
2 c. Blue
3 d. Green
7 7. Barriers UV & IR barriers
8 8. Mirror Height Controllable
9 9. Hi Magnification Lens with flipped in & out facility.
10. Apertures Adjustable for large, intermediate & small pupil.
10 11. Independent image alignment control
11 12. Original case
12 13. Teaching Mirror
14. Illumination control from head band & also from step down
transformer
13 15. Scleral Indentor Large & small with +20D aspheric lens.
5. Auto Refractometer
a) Refraction Measurement : Sphere – 25 + 25D ( 0.01/0 0.25D cylinder 0~ ±
10D (0.01/0.12) 0.25D step Axis Angle 0~ 180° (1° step).
14 b) Vertex Distance : 0, 10, 12, 13.5, 15mm
15 c) Minimum Pupil Diameter : dia 2.3mm
16 d) Pupillary Distance : Measurement range 85m (1mm step)
17 e) Printer : should have the facility to take print outs .
18 f) Internal Monitor : 5.6 inch LCD display ( color)
19 g) Movable distance : Back/force ± 17mm right/left ± 43mm, up/down ±
17mm
20 h) Movable distance of chinrest : ± 30 mm
114
7. Applanation Tonometer
1 1. It can be use for the rapid and accurate intraocular pressure
measurements.
2 2. It should have micro strain guage Transducer
3 3. The range of measurements should be 5-80 mmHg
4 4. It should have rapid scan facility at the rate of 500 samples /second.
5 5. It should have battery operating facility
8. Keratometer
1 1. It should have facility for High accuracy measurements of corneal and
contact lens radii
2 2. The facility for determination of corneal astigmatism should be there.
3 3. It should have minimum Range from 4mm to 13mm radius with
0.01mm increments.
4. It should have Halogen lamp illumination and Steel balls standard
radius for calibration.
9. Motorized Table
1 1. Instrument table can able to operate with both push button and foot
pedal
2 2. It should ensure Upward and downward movements,
3 3. It should have powder coated body
4 4. It should mount on base with four castor wheels with lock.
5 5. Height adjustment up to 16 inches approx.
1 6. It should have well finished ,good quality top.
10. A – SCAN
1 1. A scan probe - 13 MHz transducer
2 2. Scan Depth - 40-60 mm
3 3. Gain- 30-110 dB
4 4. Measurement of volume area
5 5. Accessories
i. Motorized Table
0 ii. Video/Thermal printer
1 iii. LCD Monitor
11. B – SCAN
1 1. B scan probe - 10 MHz transducer
2 2. Scan Depth - 40-60 mm
3 3. Gain- 30-110 dB
4 4. Measurement of volume area
5 5. Accessories
i. Motorized Table
115
0 ii. Video/Thermal printer
1 iii. LCD Monitor
Software
1 33. Powerful SQL database for patient’s data and images
2 34. Retina Atlas
116
3 35. Image Post processing
4 36. Brightness
5 37. Contrast
6 38. Sharpness
7 39. Smoothing
8 40. Inversion
9 41. Anti flicker
10 42. Rotation 180◦
11 43. Global grey level stretching
12 44. Zoom
13 45. Drawing
14 46. Mapping
15 47. Overlay
16 48. User friendly searching
17 49. Measurement
18 50. Tone value correction
19 51. Slideshow
1 52. Data import/export DICOM
2 53. System should allow DICOM anonymous export of patient data
/images
117
2 9. Glaucoma progression analysis and Serial Analysis for patient follow
up
3 10. Custom Static Testing, Kinetic Testing options, upgradeable software
analysis(if any),Automatic Pupil Measurement should be available
4 11. Should have fixation monitoring with
0 i. Heijll- Krakau blind spot monitor
1 ii. Video eye monitoring,
2 iii. Trial Lens Holder,
1 iv. Gaze tracking System
2 v. Head tracking
0 vi. Vertex Monitoring
1 vii. Touch screen on CRT,
3 viii. Keyboard
4 ix. Floppy drive
5 x. internal hard disk with Magneto Optical Disk (MOD) drive
for data storage
1 12. Original Manufacturer Motorized table, with Laser jet Printer
should be available.
15. Diode Laser With Lio Facility & Slit Lamp Deliverysystem
1 1. Treatment Laser Infrared diode laser (810 mm)
2 2. Cooling No external air or water cooling required
3 3. Break Power Upto 3000 mW
4 4. Aiming Laser Red diode laser variable/Hene beam
5 5. Power 0< 1.0 mw
6 6. Delivery Devices Endo Probe
7 7. Exposure Variable from 0.01 secs to continuous
8 8. Repeat interval 0.2 to 1.0 secs
9 9. It should have slit lamp delivery system facility
118
12 14. Cryo tube enhanced flexibility, 9 ft long, reduced coil memory
13 15. Probes
0 a) curved retinal probe 2.8 mm dia X17.3mm length
0 b) Curved glaucoma probe 3.4 mm dia*X19 mm length
1 c) Vitreous probe 1.5 mm dia X27 mmLength
17. Synaptophore .
Specifications:
1 1. Autoflashing device
2 2. After image test
3 3. Haidinger brushes
4 4. Slides including simultaneous macular perception
1 5. Simultaneous parafoveal perception
2 6. Simultaneous foveal perception
3 7. Set of slides for fusion
4 8. Set of slides for steropsis
5 9. Set of slides after image test
6 10. Set of slides for angle kappa
7 11. Set of slides for measurement of torsional deviation
119
20. Ophthalmic Refraction Unit
It should have the following
1 1. Motorized Up-Down Movement of the Chair.
2 2. Motorized back & forward Movement of the Chair.
3 3. Retinoscope/Opthalmoscope.
4 4. Near vision arm.
5 5. Over head reading lamp.
6 6. Indirect arm.
7 7. Sliding Table Top for Twin instrument.
8 8. The choice of either of the various colors.
9 9. Easy operation by foot control switch.
10 10. 360 degrees rotatable trial lens tray
0 11. The Smooth touch control panel to control the up/down movement as
well as 180 degree maximum to flat horizontal Inclination *
Automatically.
11 12. The 360 degrees rotable feature is for trial sets/Instruments.
12 13. The following instruments can be mounted on the table top.
0 i. Overhead lamp
1 ii. Slit lamp
0 iii. Auto-refractometer
1 iv. Ophthalmoscope/Retinoscope
2 v. Trial lens tray
3 vi. Near Vision Arm
4 vii. Chart Projector /Vision Drum
5 viii. Indirect ophthalmoscope
14. It should satisfy following
1 i. Seat minimum height- 550 mm
2 ii. Seat maximum height- 710 mm
3 iii. Up & Down stroke- 160 mm
4 iv. Seat Rotation- 0 to 180 degrees
5 v. Back & Forward movement- 95 to 175 degrees
6 vi. Power Supply- 220 V AC,50Hz
7 vii. Power consumption- 600 mA
8 viii. Load Lifting- 200 Kg
9 ix. Motor Available- 230V AC- 24 DC
10 x. Stabilizer- 0.5 KVA min
11 xi. Minimum area required- 8 feet 10 feet
12 xii. Voltage Range- 0,1.5,2.5,3.0,4.0,6.0,9.0,12.0V
120
21. Ocular Thorpe Four Mirror Gonio
1 1. Four 62 degree mirrors give a 360 degree view of the anterior chamber
angle with only slight lens rotation.
2 2. Posterior pole can be viewed through center of lens.
3 3. Lens height 32.2mm
4 4. Contact diameter 18mm.
121
It should have a 50 micron spot size setting that yields a 31 micron spot on the
iris. The lens should provide additional safety by reducing the power density at the
cornea and retina by 2.8 X.
Lens Image Laser spot Contact
height magnification magnification dia.
16.5mm 1.6X 0.63 X 15mm
29. Phacoemulsifier
1 1. Peristaltic/Venturi pump technology
2 2. Four crystal piezo electric titanium hand piece
3 3. I/A – 2 hand pieces
4 4. Ultra sound tip frequency of 29 to 40 KHZ
5 5. Ultrasound power modulation with conventional, pulse and burst
mode.
6 6. Advanced fluidics with anti surge mechanism
7 7. User friendly software
8 8. LCD touch screen and automatic IV pole option
9 9. Foot pedal with multi program options and remote control availability
10 10. Disposable and reusable tubing set / unit facility
11 11. Variable designer tips for phaco power delivery.
12 12. Phaco vacuum level 0 to 500mm in 5mm increments,
13 13. Phaco power 0 to 100% in 5% increments,
14 14. I/A vacuum range 5 to500mmHg.
15 15. Aspiration flow rate 1 to 40 cc/min.
122
16 16. High speed anterior and posterior vitrectomy and wet field bipolar
coagulator.
17 17. Customized surgeon program with different sets of parameters.
123
15 10. Apochromatic/Advance optics with anti reflex coating
16 11. Motorized zoom system
17 12. Eye piece 12.5X (10x Optional)
18 13. Beam splitter and TV adaptor
19 14. Video system
20 15. CCTV with camera attachment
33. Lensometer
1 1. Type : External Reading type
2 2. Target : Corona and cross, Rotable 360 degree
3 3. Vertex power range
0 i. (0,25 Diopter step) : 0 to +(or)- 10 Diopters
1 ii. (0,50 Diopter step) : +(or) – 10 to 25 Diopters
4 4. Cylindrical axis : 0 degree to 180 degree (1 degree steps
5 5. Prismatic power : 0 to 5 (1 step)
6 6. Acceptable Lense
1 i. Diameter : 20 to 80 mm dia.
2 ii. Tiltable angle : Continuously variable from 30 degree to 90
degree
7 7. Eyepiece focusing range : 0 to 5 Diopters
124
35 15. Lifting Capacity: 200Kgs.
36 16. Stroke Value should be 150 mm approx.
37 17. It should have Hand support, back rest & wheels
38 18. It should ergonomically Adjustable
3. Etdrs Charts
One illuminated plastic sheets printed with different size alphabets
4. Ishihara Chat
Ishihara Pseudoisochromatic Charts should be in Original form and good
quality prints. 38 plates ( complete edition )
5. Iol Kit
125
2 3. 2.75 mm slit knife
3 4. 5.2 mm slit knife
4 5. Side Port Entry knife (20G)
5 6. 1.5 mm slit
7. Surgical Instruments
126
15 15. Vannas scissors sharp tips Curved 7mm blades
16 16. Vannas scissors sharp tips Curved 10mm blades
0 17. Mcpherson westcott conjunctival scissors curved blunt tips small
blades.
17 18. Micro Corneal scissors slighty curved blunt tips small blade
18 19. Micro Corneal scissors half curved blunt tips small blade
19 20. Weiss eye speculum
20 21. Barraquer’s wire speculum small
21 22. Barraquer’s wire speculum Medium
22 23. Barraquer’s wire speculum Large
23 24. Vectis
24 25. Sinskey lens hook & manipulator
25 26. Twist hook for scleral fixation
26 27. Dastoor pupil & Irish repositer
27 28. Lens expressor
28 29. Phaco Chopper
29 30. Rycroft Air injection cannula
30 31. Simcoe irrigating aspirating cannula with silicon tube
31 32. Jenson posterior capsule polisher sand blasted olive tip
32 33. Simco cannula I/A “U” shaped for 12’0 clock
33 34. Jaffe Needle Holder
34 35. Hydro- Dissection Cannula
35 36. Towel Clip
36 37. Colibri forcep
37 38. Bone Punch
38 39. Nasal Speculum
39 40. Bone rougeur
40 41. Hammer
41 42. Chunck handle
42 43. Muller Eye speculum
43 44. Lacrimal Cannula straight
44 45. Lacrimal Cannula curved
45 46. Pigtail probe
46 47. Lacrimal probe set
47 48. Bishop forceps
48 49. Suturing forceps
49 50. Utility forceps
50 51. Cat paw Retractor
51 52. Stevens Scissors
52 53. Ring Scissors
53 54. Needle Holder
54 55. Stitch Scissors.
55 56. Enucleation Scissor half curved
56 57. Enucleation Scissor full curved
57 58. Muscle Hook
58 59. Lester – Burch Eye Speculum
59 60. Wells enucleation spoon
60 61. Bunge evisceration spoon small large
127
61 62. Mule evisceration scoop
62 63. Boll point cautery
63 64. Desmarres lid retractor
64 65. Capsulorrehxis Forcep curved shaft Utrata 85mm
65 66. Capsulorrehxis Forcep curved shaft Castroviejo 109mm
66 67. Fixation Forcep Toothed 1x2 90mm
67 68. Superior rectus Forcep toothed 115mm
68 69. Lens holding Forcep Dalgit 85mm
69 70. Castroviejo Needle Holder curved without lock 113mm
70 71. Phaco Acrylic lens folder
71 72. Phaco acrylic lens inserter
72 73. Phaco acrylic lens injector
73 74. Iris repository round ended
74 75. Sinsky hook extra fine single ended 115mm
75 76. Phaco chop cum ‘Y’ rotator 145mm
76 77. Phaco chop blunt 1mm chopping edge single ended 115mm
77 78. Scissor curved 3” 4”
78 79. scissorstraight 3” 4”
79 80. Tooth forcep straight 3” 4”
80 81. plain forcep 3” 4”
81 82. Instrument lifter 200mm
82 83. Allis tissue forcep 2x3 tooth 155mm
83 84. sponge holding forcep 200mm
1 85. Bonn Iris scissor straight sharp pointed tips 90mm
2 86. Bonn Iris scissor curved
3 87. Eye scissors Straight 115mm
4 88. Eye scissors curved
5 89. Castroviejo caliper straight 20mm
6 90. Castroviejo caliper curved 20mm
7 91. Ball cautery copper ball 6mm
8 92. Dieffenbach Bull dog clamp straight
9 93. Dastoor iris retractor 3.5mm wide for cryo
10 94. Bowman Decision needle sharp cutting edge
11 95. Graefe Iris hook tip2mm round blunt
12 96. Castrviejo Synechia spatula
1 97. Conjunctival scissor straight
2 98. Conjunctival scissor curved
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3 99. Stevens Tenotomy scissors straight round blunt tip
4 100. Stevens Tenotomy scissors Curved round blunt tip
5 101. Kalt needle holder 12mm jaw
6 102. Castroviejo Blade breaker and holder 12mm jaw
7 103. Knolle irrigating vectis angled blunt tip blunt tip
8 104. Irrigating vectis for SICS serrated tip pointed tip
9 105. Bishop- Harmon Anterior chamber wash cannula 20G
10 106. Lacrymal cannula half curved 20G
11 107. Lacrymal cannula full curved
12 108. Wildar lacrymal dilator
13 109. Nettle ship punctual dilator
14 110. Lacrymal sac Retractor Mueller
15 111. Knapp Sac Retractor 8mm wide four prongs
16 112. West bone chisel
17 113. West bone Gouge
18 114. Mallet for DCR
19 115. Kerrison bone nibbling Ronguer 1.5mm, 2mm, 3mm, 4mm, wide
20 116. Lang lacrymal sac dissector and curette
21 117. Dastoor Lacrimal sac dissector double ended
22 118. West bone gauze
23 119. Tilley Nasal packing forcep
24 120. Ferris smith punch
25 121. Citelli’s punch 1.5mm 2mm 3mm 4mm
26 122. Barkan Goniotomy knife
27 123. Toooke cornel knife Blade 3x18mm
28 124. Cyclodialysis cannula spatula Elschnig angled shaft
29 125. Kelly glaucoma punch
30 126. Goniotomy knife
31 127. Nicati foreign Body spud 26x1.25mm
32 128. Beer cilia or epliation 4.5mm long roundd platform
33 129. lambert chalazion forcep 10mm
34 130. Lambert Chalazion forcep 15mm
35 131. Desmarres Chalazion forcep 20mm
36 132. Meyer Hoefer Chlalazion curette 1.5mm
37 133. Meyer Hoefer Chalazion curette 2mm
38 134. Meyer Hoefer Chalazion curette 3mm
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39 135. Wells enucleation Spoon
40 136. Evisceration Scissor Mule
41 137. Evisceration Scissors Bunge
42 138. Kennerdell Bayonet foecep
43 139. Orbit retractor with muscle hook
44 140. Jaeger Lid plate
45 141. Stallard Ptosis plate broad
46 142. stallard Ptosis plate narrow
47 143. Swiss advancement forcep Right
48 144. Swiss advancement foecep Left
49 145. Berke ptosis multi curved shaft 20mm
50 146. Berke ptosis multi curved shaft 27mm
51 147. Snellen Entropin forceps Right
52 148. Snellen Entropin forceps Left
53 149. Knapp Strabismus scissor Straight round blunt tip
54 150. Knapp Strabismus scissor Curved round blunt tip
55 151. Graefe Strabismus hook 10.5mm
56 152. Graefe Strabismus hook 8mm
57 153. Chavasse strabismus hook curved shaft
EQUIPMENT ENT-9
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4. Optical stone forceps for smaller stones
5. Cystoscope Biopsy forceps
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6. Impedence Audiometer
1. Tympanometry Mode:
Probe frequency : 226 Hz +/- 2% typical compliance : 0.3 ml
2. Reflux mode
3. Reflux Decay Mode
4. Eustachian tube function mode
5. Display
6. Accessories :Ear tip set, Thermal Paper, Probe.
7. Auto Refractometer
Measurement mode
R mode Continuous refractometry
Ref mode Refractometry
CLBC mode Contact lense base curve measurement
Refractometry
Vertex Distance (VD) 0,10,12,13.5,15mm
Sphere (SPH) -25.00+22.00d VD= 12mm (0.12, 0.25d)
Cylinder (CYL) 0.00~±10.00d (0.12, 0.25d)
Axies (AX) 0.00~±180°
Cylinder form -,+,±
Pupil Distance 10-85mm
Minimum pupil distance 2.00mm
Measurement time 0.07 sec
Others
Internal printer Thermal printer
Power saving Selectable 3,5,10 min
Power supply AC 10 240V,50/60 Hz/90 W
Dimension/ weight 248 (W)X476(D)X475(H)m/21 Kg.
Chinrest movement Max, 55mm
Data output RS – 232 Interface, Video Output
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PD measurement 20.0 to 49.5mm (monocular), single vision PD, progressive
lens far vision PD
Measuring time 0.09 sec ± 10% (minimum)
Measurable lens diameter
Spectacle lens
Contact lens
Ф20 to 100mm
Larger than the inner diameter of the nose piece (Ф5mm)
Measurable transmittance 10% and over (20% and over for ±15 to ±25 D )
Compensation function for high index lenses
The abbe number is changeable in the range of 20 to 60
Marking system Ink cartridge type
Wavelength/ measuring point
535nm (Green)/108 with in nose piece
Display 4.7 inch colour full graphic LCD, 320 X 240 dots with a back light
Printer Thermal line printer with auto cutter (paper width : 58mm)
interface Rs – 232c : 1 PORT usb : 1 Port
Standard accessories Power cord, Dust cover, nose piece for contact lenses,
printer paper 3 rolls, operators manual, measuring progressive power lenses
explanation sheet.
Optional Accessories Eye care card, RS-232C communication cable, USB cable
(with special USB driver), foot switch, Ink Cartridge (red, Blue), Ink pad type
marking unit
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10. Ophthalmic chair unit with auto chart projector
Features
One fully upholstered elegant ophthalmic chair with full motorized recline
facilities With full motorized up & down movements for 300mm
One stand and console
With illuminating soft light for examination
With controls for ophthalmic chair
For recline and up & down
Is also provided as an additional option
Back end forward by motorized system
Specifications
Base dimensions floor space required
Height 7.6”
Length after reclining 9.6”
Width 4”
Input voltage and power 110/230V
Output 3V, 6V, 12V
Net weight 194 Kgs.
Gross weight 225 Kg.
ADD – ONS:
1. Slit lamp
2. Binocular indirect ophthalmoscope
3. Keratometer or autorefractometer
4. Direct ophthalmoscope and streak retinoscope
5. Chart projector
6. Trial lens set
7. Sight tester (phoropter)
SPECIAL FEATURES
1. Bright and clear images
2. Faster and silent operation
3. Remote operated
4. Decimal notation
5. Large choice of optotype for different diagnostic needs
6. Different masking (single, vertical and horrizontal)
TECHNICAL FEATURES
Chart : 31 Pcs
Projection Distance: 2 to 6 Meters
Supply voltage : 230V AC, 50Hz
Power consumption : 40 VA
Lamp : 6V, 20W
Net weight : 13 Kg.
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11. Cateract Set
SL. No Cataract set Quantity
1. TITANIUM Vannas 11 MM 1 No
2. TITANIUM Mcpherson forcep 1 No
3. TITANIUM Corneal Scissor 1 No
4. TITANIUM colibri 1X2 1 No
5. Sinskey hook (dialor) 2 no
6. Muscle Hook - GRAEFE 1 No
7. Superior rectus forcep- DASTOOR 1 No
8. Mosquito forcep - CURVED 1 no
9. Mosquito forceps – straight 1 no
10. Vectis plain 1 no
11. Simcoe cannula 21/22 G 1 no
12. Chopper 1.25 mm 90 Degree sharp tip 1 no
13. Phaco speculum (wire type) 1 no
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5. All attachments and hand pieces should be quick coupling & fast
interchangeable with mounted tools.
6. In built irrigation system should be available.
7. Moto should be light weight.
8. Straight and angled attachments of various lengths should available.
Sound level should be very low.
9. Quick coupling attachment should be available.
10. Single and reusableburrs should be available.
11. Sterilization through flash or regular steam autoclave.
12. Straight and angular quick coupling intra hand pieces with reduction
speed (10:1 or more), high torque should be available.
13. Power system should be supplied with
14. High speed (75000rpm or above) and slow speed motor(upto
30000rpm) motor
Irrigation unit & accessories
15. Short straight hand piece (95mm or less) high speed
16. Angular Hand piece (130mm & 160mm) high speed
17. Slow speed angular hand piece (120mm) with further reduction of 71 for
microsurgery.
18. Contra angle attachment (with inner diameter 0.8 to 1.4) for K-wire and
micro surgery.
19. Reciprocating, sagital & oscilating saw(micro and mini) hand piece and
spare saw blades.
20. Storage tray for autoclaving
21. Re-usable & single use tools
22. Diamond head (1.8mm,2.7mm,3.1mm)
23. Cylindrical Head(2.3mm)
24. Twisted drill point (1.5mm)
25. Pin point (1mm)
26. Rosen head(1.4mm,1.8mm,2.3mm,2.7mm,3mm.)
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Accessories
Slow speed angular hand piece with further reduction speed 3:1 for micro
surgery,Straight slow speed hand piece with further reduction speed of 6:1 for
Micro surgery.
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EQUIPMENT OT-10
1) Technical Specifications for Modular OT
Pre-fabricated Modular Operation Theatres Specifications
a.Objectives
The Main Objectives of Planning should be:
Promote high standard of asepsis
Ensure maximum standard of safety
Optimize utilization of OT and staff time
Optimize working conditions
Patient & Staff comfort in terms of thermal, acoustic and lighting requirements
Allow flexibility
Facilitate coordinated services
Minimizes maintenance
Ensure functional separation of spaces
Provide soothing environment
Regulates flow of traffic
b.Specifications
a) Operation Theatre Department
Structural Steel shell with joint less sealed sterile coating
- Joint less prefabricated modular Operation Theatres
- Paneled Modular Wall & Ceiling System
- Ultra Clean Ventilation Through Ceiling (Vertical laminar flow system)
b) Integrated Air & Light Theatre Ceiling
- Hermetically sealing Hospital Doors
- Static Conductive Flooring
c) Medical Gases pipeline system:- Medical Gas pipeline Equipment
d) Multi-Movement Ceiling & Wall Pendant Systems
e) Suction & Oxygen Therapy products- Bed Head Trunking System
f) Ceilings – Integral LightingSsystem
- Uniform diffusion of air into theatres
- Air and light diffusers
- Consists of plenum with conditioned air though HEPA filters.
g) AGSS – Anesthesia gas scavenging system and outlets suck the waste anaesthetic
gases
h) Hermetically sealed doors
i) Flat X-ray imaging screens step less, flicker free and dimmer
j) To provide writing board
k) Surgical scrubs sinks – elbow action taps or knee operated or flow sensor operated
l) To provide cascade pressure stabilizers
m) To provide operation theatre control panel
n) Ceiling suspension systems for monitor, anesthesia equipment surgical equipment
a) Versatile pendent (double arm) swiveling
b) Vertically movable
c) Good maneuverability
o) OT control panels
p) It should be closed circuit TV facility.
q) Service maintenance warranty for 3 years and good service backup
Floors should be smooth, non slip, impervous material conductive enough to dissipate static
electricity but not conductive enough to endanger personnel from shock. The flooring should
either be inset mosaic with least possible joints and copper strips to carry away any static
electricity produced or of joint less conductive tiles. Conductive copper mesh and self levelling
epoxy flooring may be done.
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Ceiling should be painted with washable paint and corners of the rooms should be rounded off
to prevent collection of dirt and dust.
In operating rooms anaesthetic room(s) recovery room, holding area, colour of walls and
ceilings should be such that they do not alter the observers perception of skin colour this will
facilitate patient monitoring and management.
OT should have facilities for high speed autoclaves/ sterilizers for immediate /emergency
requirements of sterilizing equipment (plate 9)
There should be a waiting room with toilet facilities for patient attendants
Pass-through cabinets that circulate clean air through them while maintaining positive air
room pressure allow transfer of supplies from outside the OR to inside it.
They help ensure the rotation of supplies in storage or can be used only for passing supplies as
needed from a clean center core (Plate 12)
There should be emergency communication system that can be activated without the use of
hands.
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b. CEILING FILTRATION SYSTEM (IMPORTED)
The ceiling filtration system should be designed to ensure unidirectional distribution of sterile air with
differential flow velocities decreasing from centre to perimeter of the surgical theatre to ensure the
cleanliness of all the area covered by the air flow. The ceiling system should be quipped with HEPA filters
with different performances according to their position in the ceiling to achieve different flow velocities.
The complete filtration ceiling system should be factory assembled its holding structure, Filter frames and
top plenum should be made of AISI 304 stainless steel. Filtration ceiling system should have HEPA filters,
H according to EN 1822 The filtration ceiling system should have flow equalizer to achieve uniform &
constant air distribution over the whole surface it should also have connection for surgical lamp to be
fitted in place of any filter. The air management system should be designed to achieved the following
parameters: F.S. 209 classification = 100 (100 particles/ft3) Bacteriological class =B (5 CFU/m3)* Particle
decontamination kinetics CP =5 min Biological decontamination kinetics CB = 5min ECG-GMP Annex 1
classification = Class A ISO 14644/1 classification = ISO 5
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7. HEPA Filter Status module
8. Room Pressure Indicator
9. Music control
Time day clock should be digital type & clocks having high brightness characters. Time Elapsed Day Clock
should be digital type & clocks having high brightness characters. Temperature indicator should indicate
the room temperature which should be connected to the local pressure switches of Air-Conditioning
System. Indicators should be digital type & clocks having high brightness characters, not less than 30 mm
in height. Central Lighting system should incorporate all the necessary controls of the lighting system
inside the theatre. The medical gas alarm should indicate High, Normal & Low gas Pressure for each gas
service present in the operating system & should have an audible buzzer with mute facility. Pressure
sensors should be connected to MGPS for monitoring the pressures. A hand free set Telephone System
should be incorporated in the panel with memory type card. The control panel should be designed for
front- access only. All internal wires should be marked with plastic Ferrule type cable markers for ease of
identification.
e. DISTRIBUTION BOARD:
All high voltage equipment should be installed in a separate enclosure. The remote cabinet should house
the operating lamp transformers, mains failure relays, electrical distribution equipment & circuit
protection equipment for all circuits within the operating theatre. All internal wiring should terminate in
connectors with screw & clamp spring connections of the clip- on type mounted, on a DIN rail & labeled
with indelible proprietary labels. Individual fees or miniature circuit breakers should protect all internal
circuits.
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perimeter passing over a concealed cove former and continuing up the wall for 100mm. All joints should
be welded with electrodes of the same compatible material to provide a continuous sealed surface. The
floor should have an electrical resistance of 2.5 * 10 to 106 Ohms, as per DIN 51953 ATM F-150 or NFPA
99, B1 class of fire resistance and should meet UL standard 779. Fulfils product requirements as per EN
649.
i. STORAGE UNIT:
The storage unit should be made with 1.50 mm thick EGP Zinc coated steel panels. The storage unit
should be divided 2 equal parts and each part should have individual glass doors with high quality locking
system. Each part will be provided with glass racks.
j. OPERATING LIST BOARD:
One operating list board should be provided in each operating theater. It should be made of ceramic
having Magnetic properties and should be flushed to the wall of the operating room.
k. HATCH BOX:
A Hatch should be provided in each operation theater to remove waste materials from the operation
theater to Dirty linen area just adjacent to Operation Theater. Each Hatch should be equipped with two
doors and the door should be operated electronically. The Hatch should be designed in such a way that
only one door should be opened at one time .The UV light should be so installed that it is kept on while
both the doors are closed, this UV light has to be automatically turned off in case of opening of either of
the doors. There shall be indicators on both side of the OT so that door open / close status can be
monitored from both ends.
l. SCRUB STATION
Compact surgical scrub sink should be designed for use in OT complex providing Surgeons with a
convenient sink for pre – OT scrub up. Each fixture should be fabricated from heavy gauge type 304
stainless steel and should be seamless welded construction, polished to a stain finish. The scrub sink
should be provided with a front access panel which should be easily removed for access to the water
controlled value, waste connections, stoppers and strainers. Hands free operation should include infra
red sensors with built-in range of adjustment. Thermostatic mixing, valve control should be located
behind the access panel and maintain constant water temperature. User defined setting of 1 to 3 min are
available. This timing should be adjustable to meet individual application requirements. Provided with
infrared sensors, thermostatic control taps with fail safe temperature controls. All units should have
reduced anti- splash fronts. Knee operated switch should be there.
m. VIEW WINDOW
The view window of specified size shall be providing consisting of: Double insulated fixed glazing with
not less than 5mm thick toughened glass. Window frame shall be powdered coated Aluminium of
approved shape flush mounted with wall paneling Motorized horizontal Venetian Blinds of powder
coated Aluminium strips of vista level or equivalent of approved shade including necessary accessories.
The motor shall be of reputed brand approved by Engineer – in – charge. The Venetian blinds should be
motorized for 90 degree rotational
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4. Should have a manual position selector, whose location should be
interchangeable between foot and head end
5. The casings on the frame and centre supporting column should be made of
hygienic stainless steel
6. Mattress should be radio lucent and suitable for fluoroscopy
7. Measurements :( all dimensions are approximated to +/_ 10 % variations)
a. Height: 730-1040 mm
b. Side tilt: + 15 degrees
c. Back section adjustment: - 15 degrees to 70 degrees
d. Foot section adjustment: - 90 to 0 degree, detachable
e. Trendelenburg: 25 degree
f. Anti trendelenburg: 25 degree
g. Head section adjustment: -40 to -30 degree, detachable
h. Maximum width: 555 mm
i. Length: 1950 mm 2.
8. Table top should be completely detachable compatible with transfer trolley
4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 Accessories should include
a. Padded arm rest with straps - pair with damps
b. Anesthesia screen with clamps
c. Side supports: pair with clamps
d. Shoulder supports: pair with clamps
e. Knee crutches: pair with damps
f. X-ray cassette tray
g. Kidney bridge
h. SS bowl with clamps
i. Infusion rod with clamp
5 Environmental factors
6 Power Supply
None
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer should be ISO certfied for quality standards.
7.3 Should have local service facility .The service provider should have the
necessary equipments recommended by the manufacturer to carry out
preventive maintenance test as per guidelines provided in the
service/maintenance manual.
7.4 Comprehensive warranty for 2 years and 5 years AMC after warranty
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job descriptin of the hospital technician and
company service engineer should be clearly spelt out.
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2.1 The light should comprise of 2 units, one major(diameter around 90 cm) and
one minor (diameter around 55 cm). Each unit should have a central light bulb.
Should have a facility of continuous brightness adjustment.Should be shadow
free
2.2 Should have provision of direct recording & display of operating field via an
autofocus, motor driven zoom lens, with digital video camera with high
definition resolution recordable on hard drive/ DVD/ Mini DV tapes. All cables
should be through the central supporting pillar of light.Each should have a single
bulb with reserve.
3 Technical Specifications
3.1 The light should be easily maneuverable and should have a swivel radius of at
least 150 cms and height adjustment of at least 100 cms
3.2 Each unit should provide more than 250000 lux light at 4200 k colour
temperature
3.3 The optimum colour temperature of the light should be between 42000 – 47000
kelvin, with colour rendering index of atleast 90.;
3.4 Each unit should provide a prefocussed beam of light with atleast 50 cms depth
of field.
3.5 It should be a cool light and should not interfere with the laminar air flow
system. The absorption of infrared radiation should be more than 99% and
infrared radiation to feet at 100000 lux should be less than 35 w per sq metre
3.6 Each unit should have halogen lamp of average life of 1000 hours – 25 spare
bulbs should be included
3.7 There should be reserve light source (halogen) with automatic activation in case
of a fuse bulb
3.8 Should have option of electro magnetic brakes to maintain the light in a steady
position
3.9 The light should have 360 degree turning radius with unbreakable head Glass.
3.10 Light should automatically switch on in case of resumption of electricity after
power failure. The handle should be Auto clavable & detachable.
4 System Configuration Accessories, spares and consumables
4.1 System as specified-
5 Environmental factors
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility.or should comply with 89/366/EEC;
EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient temperature of
10 -40deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input :220-240V/ 50 Hz AC Single phase or 380-400V AC 50 Hz
Three phase fitted with appropriate Indian plugs and sockets.
6.2 Suitable Servo controlled Stabilizer/CVT
7 Standards, Safety and Training
7.1 Should be FDA , CE,UL or BIS approved product
7.2 Manufacturer/Supplier should have ISO certification for quality standards.
7.3 Electrical safety conforms to standards for electrical safety IEC-60601-1
General Requirements
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of important spare parts and accessories with their part number and
costing.
8.4 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital technician and
company service engineer should be clearly spelt out.
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8.5 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. As per manufacturer documentation in service/technical
manual.
Suspension system:
Main light on lowermost axis position: Extension arm: 850mm (if 1 or 2 extension arms per axis)
or 700mm (if 3 extension arms per axis) respectively Length of spring arm: 930mm (iLED 5), 910mm
(iLED 3) Operating distance: 70-150cm Operating range: 2272mm (iLED 5), 2050mm (iLED 3) All arms
are freely rotatable (without stops) at all vertical joints. Number of stops: 1 (2 at iLED 3) At which joint:
connection between horizontal bow and light head (and connection between vertical and horizontal bow
with iLED 3) Rotation range joints with stop : > 400°C
Light system:
Surgical light with cold and shadow-free light, high lighting intensity and very homogeneous
large- area and in-depth illumination of the surgical field through unique multi lens matrix technology.
The colour temperature is adjustable in 4 steps from 3500K to 5000K. Within a light combination, in
order to avoid an undesirable mix of light colour from two separate light heads, when adjusting the colour
temperature on one light head, it is, as a standard setting, automatically synchronized with the other light
heads. This synchronization can be switched off and on as needed at the touch of a button. Light field
adjustment from 22cm to 30cm and focusing via steriliseable handle in the center of the light head. It is
operated by turning clock-wise in an ergonomic angle of not bigger than 45°C to reach the respective
maximum or minimum setting. All light heads can be dimmed in a range of 10% to 100%. The colour
temperature of the light remains constant in all dimming levels and is not subject to unwanted changes.
Activation and deactivation of the endo-light level (10% remaining lighting intensity) via the dimmer
control on one light head is, as a standard setting, synchronized for all other light heads within the light
combination. It can, if the need arises, be adjusted separately for each light head at the touch of a button.
Exceptional in-depth illumination and avoiding of cast shadows by means of an adjustable shadow
correction for 4 pre-defined Situation through switching on and off and adjusting the lighting intensity of
different parts of the light emitting surface respectively. (Only iLED5!)
Switching the light head on and off is possible in a sterile manner directly at the light head as well as on
the optional wall control panel. From one single control panel either only the respective light head or the
complete light combination can be switched on and off simultaneously. Switching on and off is without
any restriction in terms of holding time after switching off or with regard to the nominal light values after
switching on. No heat emission through IR radiation. High fail-safely through optical light system
consisting of 184 (iLED5) or respectively 111 (iLED3) single LEDs each with its own lens. In case of
failure of one source (LED), the illumination of the light field is not affected. Even in case of failure of a
second or more light sources, negative effects on the illumination of the surgical fields remain limited to a
minimum. Gaps and spaces between the single light emitting modules of the light head support the effect
of laminar air flow systems. Sterilizeable knob at the lower side of the light head for control of all light
function (dimming, endo-light colour temperature adjustment shadow control, switching on\off and if
applicable, camera zoom and picture rotation) by the surgical team itself (LED5!) Ligting intensity at 1 m
distance: 160,000 Lux (LED5) 130,000 Lux (LED 3) Size of light field at 1 m distance: 22-30 CM
Homogeneous light cylinder : 75 cm Colour temperature : 3500- 5000K
Colour rendering index : RA 95 Residual illumination with one shadower: 156.800 Lux (iLED 5) 94.120
Lux (iLED 3) Residual illumination with two shadower: 102.400 Lux (iLED 5) 67.600 Lux (ILED 3)
Residual illumination with tube : 147.200 lux (i LED 5) 113.100 lux (I LED 3) Resiudal illum with tube and
1 shadowder : 132.800 lux (iLEd 5) 76.700 lux (iLED3) Resiudal illum with tube and 1 shadowder: 75.000
lux (iLED5) 55.900 lux (I LED 3) Luminosity factor : 280 im/W Temperature increase at surgical site :
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max. 1o degree C Life span of main light source : > 20.000h Nominal lamp power : 184 x 1W (I LED 5) 111
X 1w (iLED 3) Power input (per light head) : 200 W (I LED 5) 120 W (iLED 3) Supply Voltage : 90- 240 V
AC, 24 V DC, 24 V AC Protection class : 1.
Light Head:
Made of powder coated aluminum diecast with smooth and clean surfaces that are easy and safely to
clean. Dust and Splash – proof One – point suspended Diamer : 823 mm (Iled 5) or 690 mm (iLED3)
respectivey Temperature at working conditions above : approx 45 degree C Underneath < 1 degree C
The light head can be pre-equipped with preparation and the respective cabling for the camera system.
Camera :
1CCD chip camera for installation either in the central handle of the light head ao at a separate carrying
arm. Control of the camera functions via external control unit . In addition , picture rotation and camera
zoom can be adjusted via the sterelisable knob at the respective light head (only iLED 5 ! )
Signal transmission and power supply via inlaying cabling with slip rings in all vertical joints.
Chip 1/6 “ CCD Standard PAL / NTSC Pixels 800,000 PAL, 680,000 NTSC Zoom 25 * optical , 12 * digital
Lens f+2.4mm(far) bis 60 mm (tele), F1.6 bis F2.7 Signal/ Noise ratio 49 dB Shuter ¼ bsi1/10000s , 20
steps(NTSC) 1/3 bis 1/10000s, 20 steps (PAL) Horizontal resolution 470 TV lines ( NTSC), 460 TV lines
( PAL) Min illumination 3.0 lux (50 IRE)
White balance automatic/ manually
Gain automatic / manually ( -3 bis 28 dB , 16 steps)
Yn-/ Outputs at the control unit :
1. 2 * Y/C (S- Video)
2. 2* FBAS(Composite)
3. Optional 1* SDI
4. Optional MPEG 2/4 via LAN connector, Further connectors
5 1* LAN connector ( RJ 45)
6 1* Serial interface (RS 232 or 485-)
7 Optional 1* USB
8 Optional 1* Audio in/out
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(15) It should stabilize less than 3 sec. & should rebooted less than 1 min.
(16) Camera should be independent of microscope.
(17) there should be a facility of a manual balance.
3.2 Essential Accessories:
(1) Stereoscopic coobservation attachment for second observer with
tiltable eyepieces, minimum 0-160 Deg.
(2) Integrated Beam Splitter
(3) 3-Chip CCD HD (high definition) output camera with c-mount for
connecting with the microscope & recording on a hard drive on mini DV
disks.
(4) Digital video recording facility with appropriate video editing software.
3.3 Optional Accessories:
(1) Diploscope (face to face attachment)
(2) 12-function footswitch
(3) Digital still camera for attachment with microscope
5 Environmental factors
5.1 The unit shall be capable of being stored continuously in ambient temperature of 0-
50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating in ambient temperature of 20-30 deg C and
relative humidity of less than 70%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Resettable overcurrent breaker shall be fitted for protection
6.3 Voltage corrector /stabilizer of appropriate ratings meeting ISI Specifications. (Input
160-260 V and output 220-240 V and 50 Hz)
6.4 Suitable UPS with maintenance free batteries for minimum one-hour backup should be
supplied with the system.
8 Documentation
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine maintenance support
as per manufacturer documentation in service / technical manual.
8.4 List of important spare parts and accessories with their part number and costing
8.5 Log book with instructions for daily, weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service engineer
should be clearly spelt out.
8.6 Compliance Report to be submitted in a tabulated and point wise manner clearly
mentioning the page/para number of original catalogue/data sheet. Any point, if not
substantiated with authenticated catalogue/manual, will not be considered.
7. O.T .TABLE
It should satisfy following Specifications
1. Suitable for ophthalmic surgery
147
2. Motorized
3. It should have Head rest and wrist support.
4. Maximum height : 900 mm approx.
5. Minimum Height : 580 mm approx.
6. It should have height adjustment facility. The approximate range for Height adjustment
should be 300 mm.
7. Length : 1900 mm approx.
8. Width : 700 mm approx.
9. Trendelenberg : 28 degree approx.
10. Reverse Trendelenberg : 15 degree approx.
11. It should have facility for instrument tray.
8. O.T .LIGHT
1 The light should comprise of 2 units,
i. one major which should have output between 120 k lux and 160 k lux
ii. One minor which should have output between 80 k lux and 100 k lux.
2 Each unit should have a central light bulb.
3 Should have a facility of continuous brightness adjustment.
4 Should be shadow free.
5 It should be multiple or single reflector Prismatic or Optical Block based system.
6 Should have provision of direct recording & display of operating field via an auto focus,
motor driven zoom lens, with digital video camera with high definition resolution
recordable on hard drive/ DVD/ Mini DV tapes. Preferably mounted into the sterilizeable
handle.
7 All cables should be through the central supporting pillar/column of light.
8 Should have dichroic mirrors and KG type glass filter for better thermal filtration so that
the light on the incident area is free from thermal properties and cold.
9 Bulbs should should be of standard Quartz Halogen 12/24 V ;50,75,100,150 Watts 2 pin
base. Nonstandard bulb with special f product which is using proprietary items such as
bulbs with special pins or wings with clips or base should not be considered because of
non-availability of such items in the market.
10 Changing of bulbs should be easy with no tools or with very simple tools like screw
drivers only and bulb base mounting should be independent of the sterilizable handles.
11 Changing of bulbs should not take more than 3-5 minutes.
12 The increase in the ambient temp of the room with the lights on should not be more than
3-5 degrees centigrade.
13 The light should be easily maneuverable and should have a swivel radius of at least 150
cms and height adjustment of at least 100 cms
14 The optimum colour temperature of the light should be between 3400-4200 Kelvin, with
colour rendering index of at least 90%
15 Each unit should provide a pre-focused beam of light with at least 50 cms depth of
field.
16 It should be a cool light and should not interfere with the laminar air flow system. The
absorption of infrared radiation should be more than 95% and infrared radiation to feet
at 100000 lux should be less than 35 w /sq meter
17 Each unit should have quartz halogen lamp of average life of 1000 hours
18 25 numbers of spare bulbs should be included
19 The light should have 360 degree turning radius with unbreakable head Glass.
20 Light should have battery back up automatic switch over facility
21 The handle should be Autoclavable & detachable.
22 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements of Safety for
Electromagnetic Compatibility. Or should comply with 89/366/EEC; EMC-directive.
23 The unit shall be capable of being stored continuously in ambient temperature of 0
-50deg C and relative humidity of 15-90%
24 The unit shall be capable of operating continuously in ambient temperature of 10 -40deg
C and relative humidity of 15-90%
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25 It should be fitted with appropriate Indian plugs and sockets.
26 It should have Suitable Servo controlled Stabilizer
27 It should conforms to standards for electrical safety IEC-60601-1 General
Requirements
28 It should supply with User/Technical/Maintenance manuals in English.
29 It should be supplied with Certificate of calibration and inspection.
30 List of important spare parts and accessories with their part number and costing should
beattached.
31 Log book with instructions for daily, weekly, monthly and quarterly maintenance
checklist should be attached. The job description of the hospital technician and company
service engineer should be clearly spelt out.
32 List of Equipments available for providing calibration and routine Preventive
Maintenance Support should be attached, as per manufacturer documentation in
service/technical manual.
9. BOYLE’S APPARATUS
1. Boyle’s Apparatus should have rigid steel structure with four antistatic castors wheels
having front with brakes.
2. It should have Appro. (10”) long rotating bobbin flow meters, (rotameters) with colour
coded control knobs, calibrated in multiple scales for accurate reading.
3. It should have Oxygen (1st tube)-10 cc/mm to 3.5 liter/min
4. It should have Oxygen (2nd tube)- 3.5 liter/min to 10 liter/min
5. It should have Nitrous oxide (1st tube)- 200 cc/ min to 5 liter/min
6. It should have Nitrous oxide (2nd tube)- 5 liter / min to 12 liter/min
7. It should have Air-100 cc/min to 12 liter/min
8. It should have It should be Gas specific, gas blocks pin indexed yokes, two each for
oxygen & nitrous oxide & one for air suitable for pin- indexed cylinder. The equipment
shall also have attachment for connection of compressed air.
9. It should be Fitted with pressure gauges 100 mm diameter mounted on O2 and N2O
cylinder (2 each) for clear visibility.
10. It should have Vaporizer for ether, penlon type with graduated jar with mounted
selectatec. There should be Temperature compensated vaporizer for
halothane/isoflourine {optional}
11. It should be Fitted with regulators and non return cum pressure release valves for gases.
12. It should have Two Numbers oxygen pneumatic power outlets operating at 50 psi to
operate ventilator.
13. It should have Extended rear platform for mounting two nos additional 10 litre water
capacity cylinders.
14. It should have Patient circuit to include elephantine tubing reservoirs bag, connections
for changeover from open to closed circuit and vice versa.
15. It should have Top tray for monitoring equipment
16. It should have Drawer for keeping instruments.
17. In other respects the equipment shall comply with IS-11378-1985.
18. It should have adjustable pressure limiting valve, breathing circuit pressure measuring
device.
19. It should have a bag/ventilator selecting valve integrated onto the absorber.
20. It should be suitable to use low flow techniques - Facility to attach oxygen sensor.
21. It should have CO2 absorbent Dual chamber canister
22. It should have Automatic cutoff of nitrous oxide in case of oxygen supply {nitro lock
system}falls.
23. It should have Pneumatic device with audible alarm mechanical (not electrical) when
oxygen supply falls to 10-15 psi.
24. It should have Hypoxic safety device to ensure that the patient is never subjected to pure
N2O in flow out doses (shall ensure protection against singular flow of N2O) until a
minimum flow of 1 liter-1.5 liter oxygen released.
25. Unit shall incorporate optional oxygen analyzer (oxygen concentration level indicator).
26. The Regulator and Yoke should force with S.S fittings.
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27. The machine should have 3 inlets for O2 and N2O
28. It should have 2 oxygen outlets{optional}
29. There should at least one operating pressure gauge for O2 and N2O separately.
30. The operating pressure should be 4.22 kgf/sq.cm +/-0.5%
31. There shall be provision of adequate supply of oxygen to the patient even if the flow
meter knobs are fully turned off.
32. Unit shall conform to relevant safety standards and general safety standards as per IS-
8607.
11. Operation Theater Light Halogen Twin (Seven Bulb + Four bulb)
150
Dome B (Four Bulb)
Ceiling model With Spring Arm
Dome head: 515mm dia
Halogen Bulb: 4nos. 12x50watt
Light intensity at 1mt. 70,000 Lux
Intensity control 4 stage
Height adjustment 550mm
Action radius 1550mm
Possible movements radial angular & axial
Color temperature 4200k +- 300k
Temp. Rise in field 3’ – 6’c from amb. Temp.
Low voltage unit with CVT: 1nos
Input Supply voltage: 220volt A.C+-10% 50Hz+-2%
dismantle & reassemble, shock-proof energy saving halogen bulbs with minimum 500-1000
hours life, light intensity of 1250 foot candles at 16inch dia small spot for more accurate
diagnosis lamp head is compact and detachable lamp light temperature is kept at 3400 Kelvin
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EQUIPMENT PAEDTRACIS -11
2 Operational Requirements
2.1 High quality with humidity and servo controlled double walled with cabinet
incubator.
2.2 Microprocessor controlled, easy access control panel with feather touch
switches
2.3 With a facility to elevate base to offer adjustable range
2.4 Facility with both servo control as well as air temperature control and servo
humidifier
2.5 Accommodates shelves and IV poles.
2.6 The quality of the material used should very high and crystal transparent
2.7 Super quality microprocessor based control system - self test functions are
performed
2.8 System required complete with Oxygen port with tubing and Gel Mattress.
3 Technical Specifications
3.1 Continuous bed tilt up to 8° on either sides
3.2 Head end raise facility with auto lock.
3.3 Both visual and audible alarms for
(i) Patient and control and high / low temperature alarm.
(ii) Air circulation / probe / system / power failure alarm.
(iii) Humidity control alarm.
3.4 Facility to take x-ray and weight without removing baby.
3.5 Facility to display and trends of temperature information on compatible
monitors with other physiological parameter.
3.6 Height 140 cm + 5 cm, depth at least 60 mm , width at least 90 mm. Mattress to
hood distance 40 cm working level – 90 to 100 cm. Iris port for tubing, probes,
leads. 4cm thick gel mattress, easily cleanable. With at least 4” diameter caster
wheel with swivel in all directions and with front lockable wheels. Two shelves
cabinet with door. Weight 90-100 kg.
3.7 Patient control (Servo) mode – 35 deg-37 deg C. and Air Control (Manual mode)-
20 deg C to 39 deg C
3.9 Air velocity less than 10 cm/sec with inner wall.
3.10 Temperature variability less than +/-0.2 deg C and Temperature resolution +/-
1 deg C
3.11 Humidification. Standard: 10-75% dependent on nursery environment and
incubator temperature setting. Servo: 40-80% regardless of nursery
environment.
3.12 Double wall canopy with Four hand ports with elbow operated flaps.
3.13 C02 flushing, according to lEC 601-2-19 / 105.1
Maximum C02 concentration inside incubator 0.2%
3.14 Servo control for Oxygen with integrated monitoring
3.15 Noise level < 49 dB
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4 System Configuration Accessories, spares and consumables
4.1 System as specified
4.2 Two sets of extra non disposable sensors.
5 Environmental factors
5.1 Shall meet IEC-60601-1-2:2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility or should comply with 89/366/EEC;
EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient temperature of
10 -40 deg C and relative humidity of 15-90%
6 Power Supply
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI Specifications.
( Input 160-260 V and output 220-240 V and 50 Hz)
8 Documentation to be provided.
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spares and accessories with their part number and costing.
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job descriptin of the hospital technician and
company service engineer should be clearly spelt out.
1 DESCRIPTION OF FUNCTION
1.1 An infant incubator provides a closed, controlled environment that warms an
infant by circulating heated air over the skin. The heat is then absorbed into the
body by tissue conduction and blood convection. Ideally, both the skin and core
temperatures should be maintained with only minor variations.
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2 OPERATIONAL REQUIREMENTS
2.1 High quality with humidity and servo controlled double walled with cabinet
incubator.
2.2 Microprocessor controlled, easy access control panel with feather touch
switches
2.3 With a facility to elevate base to offer adjustable range
2.4 Facility with both servo control as well as air temperature control and servo
humidifier
2.5 Accommodates shelves and IV poles.
2.6 The quality of the material used should very high and crystal transparent
2.7 Super quality microprocessor based control system - self test functions are
performed
2.8 System required complete with Oxygen port with tubing and Gel Mattress.
3. TECHNICAL SPECIFICATIONS
3.1 Continuous bed tilt up to 8° on either sides
3.2 Head end raise facility with auto lock.
3.3 Both visual and audible alarms for
(i) Patient and control and high / low temperature alarm.
(ii) Air circulation / probe / system / power failure alarm.
(iii) Humidity control alarm.
3.4 Facility to take x-ray and weight without removing baby.
3.5 Facility to display and trends of temperature information on compatible
monitors with other physiological parameter
3. 6 Height 140 cm + 5 cm, depth at least 60 mm , width at least 90 mm. Mattress to
hood distance 40 cm working level – 90 to 100 cm.
Iris port for tubing, probes, leads.
4cm thick gel mattress, easily cleanable.
With at least 4” diameter caster wheel with swivel in all directions and with
front lockable wheels. Two shelves cabinet with door.
Weight 90-100 kg.
3.7 Patient control (Servo) mode – 35 deg-37 deg C. and Air Control (Manual mode)-
20 deg C to 39 deg C
3.8 Air velocity less than 10 cm/sec with inner wall.
3.9 Temperature variability less than +/-0.2 deg C. and Temperature resolution
0.1 deg C
3.10 Average oxygen input concentration range 5-15 liters/min or 25-70%.
3.11 Humidification adjustable electronically with digital display . Standard: 10-80%
dependent on nursery environment and incubator temperature setting.
3.12 Double wall canopy with Six hand ports with elbow operated flaps with separate
ports for tubing.
3.13 CO2 flushing, according to lEC 601-2-19 / 105.1 Maximum C02 concentration
inside incubator 0.2%
3.14 Servo control for Oxygen with integrated monitoring
3.15 Noise level < 49 dB
3.16 Air filter :- 0.3 micron
3.17 Built in weighing scale with sensitivity of + 1 gm
3.18 Mattress should be radiolucent
3.19 Provision for X ray cassette holders
3.20 2 drawer storage facility and two platforms for keeping monitors , able to bear
at least 5 kg weight each.
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4.2 Two sets of extra non disposable temperature sensors and humidification
sensors.
5 ENVIRONMENTAL FACTORS
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility or should comply with 89/366/EEC;
EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient temperature of
10 -40 deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI Specifications.
( Input 160-260 V and output 220-240 V and 50 Hz)
8 DOCUMENTATIONS TO BE PROVIDED
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spares and accessories with their part number and costing.
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job descriptin of the hospital technician and
company service engineer should be clearly spelt out.
1 DESCRIPTION OF FUNCTION
1.1 Required for transportation of premature babies and neonates and it can be
used for long distance transportation.
155
2 OPERATIONAL REQUIREMENTS
2.1 It should be mobile intensive care station including transport ventilator,
monitors, incubator, rechargeable power supply unit and infusion stand
3 TECHNICAL SPECIFICATIONS
3.1 It should be mounted on collapsible trolley having lockable rust free castors of
the size 4 inches or more and with facility to mount two A type Aluminum
oxygen cylinders on rack under the Incubator .
3.2 Single walled incubator with at least two large port holes for access. Iris ports
for ventilator & other tubings. Bed level at least 80 cms. above ground level. Two
shelves cabinet with door.
3-3 Width: app 80 cm+ 5 cms. , Depth 30 cm + 5 cm, height 115 + 5 cms,
Mattress to hood distance at least 30 cms.
3.2 Air Mode: adjustable set temperatures between 20 – 39 C. Display of set
temperatures with resolution of 0.1 C. Skin mode adjustable set temperatures
between 34 – 38 C. Display of set temperatures with resolution of 0.1 C. 3.3
Alarms of High , Low and Probe failure for the set air mode up to +2.5 C and skin
mode of + 0.5 C of temperatures
3.4 Oxygen monitor in incubator hood with display of 21 – 100% Oxygen alarms for
high, low and probe failure.
3.5 Heart and Oxygen saturation monitor: Fixed, built monitors, dual wavelength
probe for Oxygen saturation with Digital LED display for Heart rate and Oxygen
saturation. Alarms for high and low for Heart Rate, Oxygen saturation and probe
failure
3.6 The system should have an internal rechargeable maintainence free battery to
ensure continued functioning of the unit for at least 4 hours during transport. It
should have automatic switch circuit for change over from battery to AC and
vice versa.
3.7 One suction apparatus with negative suction pressure of 5- 120 mm Hg should
be provided. IV fluid stand should support two infusion bottles
3.8 One Syringe infusion pump with stand compatible with 10, 20, and 50 ml
syringes compatible with locally available brand of syringes. Range of infusion
rate 1 – 99 ml / hr.in steps of 0.1ml. Display infusion rates, Alarms for
occlusions, end of infusion with internal rechargeable battery should be
provided along with the quoted price
3.9 Height less than 60”, depth less than 30”, width 33”-36”. Weight 90-100 kg.
With wheel mounted. (All dimensions in approximation of +/-10%)
3.9 VENTILLATOR SPECIFICATIONS:
a. The ventilator should provide IPPV, IMV, CPAP, SIMV and PEEP
modes.
b. It should be time cycled, pressure limited transport ventilator. It should
be capable of setting the parameters of PIP, PEEP, VR, Ti, FiO2 and flow.
c. There should build in oxygen/air mixer with monitoring facility.
d. It should have facility for integrated airway monitoring.
e. There should be battery back up for 4 hours
g. Alarm function should include audio visual alarm for high pressure, low
pressure, fall- to-cycle, low battery and gas mixture failure.
h. There should be choice to select frequency up to 100 bpm.
i. There should be built in noise free air compressor with filters for
appropriate medical usage.
j. There should be provision for continuous flow in IMV and CPAP modes
and should have reduced flow during expiration in IPPV mode
k. It should have automatic reciprocal gas-supply compensation of air
supplementation from environment in case of oxygen supply failure.
l. There should be digital display of PIP, PEEP, MAP and BPM.
m.A resuscitator to provide manual ventilation with mask should be
supplied along with the quoted price.
156
3.10 There should be provision for bronchial suction with adjustable negative
pressure 0-5 bars and gas consumption should not be more than app 7 liters per
minute
3.11 The unit should have built in shock absorbers to cut off ay vibration and should
be fitted with safety device
5 ENVIRONMENTAL FACTORS
5.1 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility.or should comply with
89/366/EEC;EMC-directive.
5.2 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.3 The unit shall be capable of operating continuously in ambient temperature of
10 -40 deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz
6.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI Specifications.
(Input 160-260 V and output 220-240 V and 50 Hz)
8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. As per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily, weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
engineer should be clearly spelt out
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4. Equipment Specifications for Ventilators Neonatal
1 DESCRIPTION OF FUNCTION
1.1 For ventilating neonates, pre mature and infants babies.
2 OPERATIONAL REQUIREMENTS
2.1 System with battery back up is required.
3 TECHNICAL SPECIFICATIONS
3.1
1. Essentials Ventilator Air Compressor Reusable Circuit with online bacterial filter
Humidifier
Stand for circuit
Operator manual
Service manual
2. Type of ventilator Continuous flow, time cycled, pressure limited
3. Modes available CPAP, IMV, SIMV, Assist/Control, PSV, Volume Guarantee,
Triggers, Flow & Volume triggers
4. Range of set parameters
Peak inspiratory pressure 0-50 cms
Positive end expiratory pressure 0-20 cms
Fraction of inspired oxygen 21-100%
Inspiratory time 0.1- 3 secs
Rate 0-150 bpm
Gas flow 5-15 Lpm
5. Display Both digital and analog All set parameters as mentioned above
Measured parameters
PIP, PEEP, Mean airway pressure
FiO2
Ventilator rate
Derived parameters
Te, I:E ratio
Leak percentage
Tidal volume
Minute ventilation
Pressure & flow waveforms and loops
Alarm message
Calibration
Silenced alarm
6. Alarms Both audio & visual
Low & high pressure – PIP , PEEP separate
Compressor failure
Failure of sensor/s
Tube obstructed
Power failure
Alarm ventilator failure
7. Humidifier Heater with Flow resistance upto 1 cm H2O/L/Sec
Temperature up to 39 degrees C
Temperature control + 2C Warm
Digital display of temperature- range of display 5-40C
Water level indicator
Warm up time less than 15 minutes
Alarms
Heater wire on:
158
Airway temp: Tracking + 2C from set temp
Chamber temp: If chamber temp varies +4C from set temp for 20 minutes or
alarms immediately if set chamber is exceeded by 1C
Heater wire off:
Airway temp: Fixed at 41C high & 29.5 C Low
Chamber temp: limited to 60C max
Should be compatible with both reusable & disposable chambers and reusable &
disposable circuits
Flow / pressure sensor- 20 each
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 - 40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
159
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily , weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
engineer should be clearly spelt out
1 DESCRIPTION OF FUNCTION
1.1 Required for care of new born and infants
2 OPERATIONAL REQUIREMENTS
2.1 Complete system with cart and oxygenation facility is required.
3 TECHNICAL SPECIFICATIONS
3.1 Essential parts : Cart & bassinet
Warming system with controls & alarms
Examination light
Storage space- 2 sliding drawers below
bassinet 2 platforms of the size 9” x 12” capable of holding up to 5 Kgms of
equipments
Cart: Should swivel on 4 wheels of at least 5” dia- with foot operated., 2 front
lockable wheels.
Dimensions
Height : 180-200 cms
Width : 60-70 cms
Depth : 100-120 cms
Working level : 95-110 cms and adjustable
Bassinet : 1 fixed and 3 movable transparent side walls:Portion above X-Ray
cassette holder radiolucent Mattress
Width : 55 – 60 cms
Length : 65- 70 cms
Thickness : Minimum 4 cms
Material : Soft, Comfortable, easy to clean, radiolucent
Bassinet tilt in steps of 6 – 8 degrees, Trendelenburg or reverse Trendelenburg
Warmer module swivel : 45-65 degrees on either side
Warming systems
Modes :Manual & skin
Manual mode :Adjustable in steps from zero to 100
Skin mode
Method : Flexible, unbreakable skin temperature probe Set
point range : 34 – 38 degrees C
Skin temp variability at Temperature equilibrium :+ 0.2 degrees C
Skin temperature display
Accuracy : + 0.2 degrees C
Type : digital LED with 0.1 degree resolution
Correlation of displayed And actual skin temp : difference 0.2 degrees C
Silence/ Reset switch : To silence the alarm & reset set point
Alarms: Probe failure
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Heat failure
High and low temperature
Power failure
System failure
Examination light : Illuminance 100 foot candles at mattress center
Storage space : 2 drawers, preferably covered and sliding
Pulse oximeter : to measure oxygen saturation and heart rate resistant to
motion artifact. Able to pick up signals in low perfusion states.
CPAP system : Flow driven With air oxygen blender and FiO2 control, with
heated humidifier, airway pressure display 0-15 cm H2O, With bonnet, cap and
nasal prongs (10 of each size) for babies 600 gm-4000 gms, with reusable
circuits, with 1 reusable flow generator
Power requirements : 220/240 V AC, 50/60 Hz,
Accessories
I.V. line pole with pivot bracket : should be able to accommodate 2 fluid bottles
Monitor shelves : 2 in number
: Should support upto approx. 20 kgs per shelf or upto 25 kgs total on single side
Standard X- Ray cassette holder : sliding holder located just below
undersurface of Bassinet, with markings to help placement of cassette
Patient Probes : 4 reusable temperature probes
4 reusable oxygen saturation probes
2 patient extension cables for the saturation probes
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 - 40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
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8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily , weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
engineer should be clearly spelt out
1 DESCRIPTION OF FUNCTION
1.1 Phototherapy units are used to treat hyperbilirubinemia, a condition
characterized by high bilirubin concentrations in the blood.These units are also
called: bilirubin lamps, bilirubin lights, fiberoptic phototherapy blankets,
neonatal phototherapy units
2 OPERATIONAL REQUIREMENTS
2.1 Should be Compact Florescent Lamp (CFL) based Phototherapy unit used for
clinical management of neonatal hyperbilirubinemia
2.2 Lamp unit should be made with plastic lamp module with metallic top cover for
efficient heat dissipation to reduce radiant heat on infant.
2.3 Should occupy very little bedside space, offer convenience in observation and
procedures
2.4 The unit should be mobile with 3 swivel castors of 2” diameter fixed to a
Tshaped base to be accommodated beneath trolley/bed with adjustable height.
3 TECHNICAL SPECIFICATION
3.1 Irradiance at 430 – 480 nm- effective to the baby of at least 18 mw/cm/nm at
45cm from the lamp.
3.2 Lamps: compact florescent lamps
3.3 Height adjustable:(app+/-5 cm): 138cm (minimum) – 190 cm (maximum)
3.4 Lamp tiltability :- horizontal to vertical at any angle.
3.5 Time totaliser : Mechanical / Electronic
3.6 Therapy duration timer: Resettable – optional
3.7 Height of the base app: 6-8 cm (at the front)
3.8 Size of the lamp unit (LxBxH) 47 x 40 x 9 cm +/- 5 cm
3.9 Coating: Epoxy / Powder coated body for scratch and rust prevention
162
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 -40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
8 DOCUMENTATIONS TO BE PROVIDED
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital technician and
company service engineer should be clearly spelt out.
1 DESCRIPTION OF FUNCTION
1.1 Phototherapy units are used to treat hyperbilirubinemia, a condition
characterized by high bilirubin concentrations in the blood.These units are also
called: bilirubin lamps, bilirubin lights, fiberoptic phototherapy blankets,
neonatal phototherapy units
2 OPERATIONAL REQUIREMENTS
2.1 Should be Tube light based Phototherapy unit used for clinical management of
neonatal hyperbilirubinemia
2.2 Lamp unit should be made with metallic lamp module with metallic top cover
for efficient heat dissipation to reduce radiant heat on infant.
163
2.3 Should occupy very little bedside space, offers convenience in observation and
procedures
2.4 The unit should be mobile with 3 swivel castors of 2” diameter fixed to a
Tshaped base to be accommodated beneath trolley/bed with adjustable light.
3 TECHNICAL SPECIFICATIONS
3.1 Dimensions
Height :- adjustable with upper limit at least going up to 1570 mm
Width :- 730 mm +10 mm
Length :- 500 + 10 mm
3.2 Irradiance at 430 – 480 nm-- effective to the baby of atleast 18 mw/cm/nm at
45cm from the lamp.
3.3 Lamps: (6 Blue) compact florescent lamps ( of 20 wt. Each) of TL 52 (Philips) or
equivalent.
3.4 Lamp tiltability :- horizontal to vertical at any angle
3.5 Time totaliser : Mechanical / Electronic
3.6 Therapy duration timer: Resettable – optional
3.7 Height of the base app: 6-8 cm (at the front)
3.8 Coating: Epoxy / Power coated body for scratch and rust prevention
3.9 Ballastic chocks should be located at the base to decrease the heat and increase
the stability of the unit.
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 -40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
164
8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job descriptin of the hospital technician and
company service engineer should be clearly spelt out.
1 DESCRIPTION OF FUNCTION
1.1 Phototherapy units are used to treat hyperbilirubinemia, a condition
characterized by high bilirubin concentrations in the blood.These units are also called:
bilirubin lamps, bilirubin lights, fiberoptic phototherapy blankets, neonatal
phototherapy units
2 OPERATIONAL REQUIREMENTS
2.1 Fibreoptic phototherapy for greater uniformity of radiation
2.2 Compact and smaller sized equipment than conventional phototherapy.
3 TECHNICAL SPECIFICATIONS
3.1 Bili light lamp with fibre optic cable and optic fibre pad of size 22 x 10.5 cms +/-
10%
3.2 Halogen lamp optic assembly.
3.3 Special group of filters to screen heat and filter ultra violet rays
3.4 Emitted radiation to have wave length between 425-475 nm.
3.5 Light beam to be conveyed to patient through optic fibre cable and a pad.
3.6 The pad to be sealed, waterproof and hygienic.
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 to 40 deg C and relative humidity of 15-90%
165
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
8 DOCUMENTATIONS TO BE PROVIDED
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and costing
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital technician and
company service engineer should be clearly spelt out.
1 DESCRIPTION OF FUNCTION
1.1 Phototherapy units are used to treat hyperbilirubinemia, a condition
characterized by high bilirubin concentrations in the blood.These units are also called:
bilirubin lamps, bilirubin lights, fiberoptic phototherapy blankets, neonatal
phototherapy units
2 OPERATIONAL REQUIREMENTS
2.1 Should be Tube light based Phototherapy unit used for clinical management of
neonatal hyperbilirubinemia
2.2 Lamp unit should be made with metallic lamp module with metallic top cover
for efficient heat dissipation to reduce radiant heat on infant.
2.3 Should occupy very little bedside space, offers convenience in observation and
procedures
2.4 The unit should be mobile with 3 swivel castors of 2” diameter fixed to a
Tshaped base to be accommodated beneath trolley/bed with adjustable height.
The bassinet unit should be mounted on four swivel castor of four inch dia. And
should be able to move independently of the top unit.
3 TECHNICAL SPECIFICATIONS
3.1 Dimensions
166
Height :- adjustable with upper limit at least going up to 1570 mm
Width :- 730 mm +10 mm
Length :- 500 + 10 mm
Bassinet unit
Height :- 1015 mm + 10 mm
Width :- 750 mm +10 mm
Length :- 525 + 10 mm
Transparent cabinet with two collapsible walls.
3.2 Irradiance at 430 – 480 nm-- effective to the baby of at least 18 mw/cm/nm at
45cm from the lamp.
3.3 Lamps: (6 Blue) tube lights of 20 watts. Each of TL 52 (Philips) or equivalent for
each unit.
3.5 Time totaliser : Electronic
3.6 Therapy duration timer: Resettable
3.7 base unit approx.: 6-8 cm from the mattress unit.
3.8 Coating: Epoxy / Powder coated body for scratch and rust prevention
3.9 Ballastic chocks should be located at the base to decrease the heat and increase
the stability of the unit.
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 to 40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
167
8 DOCUMENTATIONS TO BE PROVIDED.
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job description of the hospital technician and
company service engineer should be clearly spelt out.
1 DESCRIPTION OF FUNCTION
1.1 Electronic weighing balances are required to weigh the baby weight accurately.
2 OPERATIONAL REQUIREMENTS
2.1 Accurate and rugged system is required
3 TECHNICAL SPECIFICATIONS
3.1
Digital weighing scale
Range 0-10 kg
Accuracy : + 5 grams
Display : Bright up to 3 decimal points
Units : in grams/kg
Baby pan/platform : 50 cm x 30 cm +/– 10 %
Easily cleaned and disinfected Tare facility
Should be able to stabilize the readings in spite of baby movements
Memory : Up to 10 readings
Mounting : On a lightweight compact mobile trolley
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 -40deg C and relative humidity of 15-90%
168
6 POWER SUPPLY
6.1 Power supply : 220/240V 50/60 Hz with DC adaptor. Capable of running on
battery
8 DOCUMENTATIONS TO BE PROVIDED
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily , weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
engineer should be clearly spelt out
1 DESCRIPTION OF FUNCTION
1.1 Laproscopic surgery in Paediatrics
2 OPERATIONAL REQUIREMENTS
2.1 3 Chip Camera
2.2 Video processor
2.3 Insufflator
2.4 Telescope
2.5 Instruments
2.6 Accessories
3 TECHNICAL SPECIFICATIONS
3.1 - 3 Chip Camera
1. Integrated zoom lens
2. F25- 50 mm
3. Beam splitter
4. Digital zoom
5. Freeze frame facilities
6. With digital video
7. With DV cable
3.2 Video processor
1. Hi definition Video 1289 x 1024 native resolution
2. Control of the two peripheral accessories at camera head
3. One standard RGB output
169
4. S VHS output - 2 Nos
5. S VHS (Video composits) output – 2 Nos
3.3 Insufflator
1. 20 litres advance continuous electronic CO2, flow technology (not
intermittent flow) should not have any disruption between gas flow and
pressure reading.
2. Digital decimal (0.1 Resolution) display of flow and pressure
parameters.
3. User selectable safely blow off pressure settings
4. Pressure releasing mechanism should be controlled by in built software
5. Measurement of pressure up to 50 mm of mercury
6. Desirable – Thermal Insufflator system
3.4 Telescope
1. Rod – lens technology 5 mm 0o , length 24 cm ( 1No)
2. Rod lens technology 5 mm 30o length 24 cm(1 No)
3. Autoclavable and wide angled.
3.5 Instruments
1. 3 mm dissecting and grasping forceps, double action jaws, length 20 cm
–1
2. 3 mm dissecting and grasping forceps heavy, double action jaws, length
20 cm – 1
3. 3 mm dissecting and grasping forceps with ratchet single action jaws
with atraumatic fine serration – 2
4. 5 mm size tracar with conical tip, cannula with LUER lock connection
forinsufflation length 5 cm, silicon leaflet valves – 2
5. 3 mm size tracar with conical tip, cannula with LUER lock connection
for insufflation length 5 cm, silicon leaflet valves – 2
6. 10 mm size tracar with conical tip, cannula with LUER lock connection
for insufflation length 5 cm, silicon leaflet valves – 2
7. 3 mm scissors length 20 cm with serrated jaws curved conical double
action jaws. - 1
8. 3 mm scissors length 20 cm single action jaws- 1
9. 3 mm coagulation and dissection electrode length 20 cm L shaped
insulated with connector pin for unipolar coagulation - 1
10. 3 mm palpation probe distendable length 20 cm – 1
11. 3 mm micro needle holder handle with rachet length 20 cm – 1
12. Irriagation and suction cannula with 2 way stop cock – 1
13. 2 way stop cock -1
14. 3 mm pylorotome length 20 cm distendable – 1
15. knot guide with eyelet – 1
16. Clip applicator
170
1. 220 volts, 300 watt, Xenon/ Halogen (twin Bulb) with elliptical Bulb
design
2. Bulb working life 500 hrs
3. Bulb life counter on light source
4. Automatic light Adjustment
5. Stand by button
6. universal jaw assembly to adapt any make of Fiber optic
7. cable without adapter with single hand operation
8. Automatic shutter
9. Spare bulbs – 2
10. Spare light cable 2
3. Medical grade LCD Monitor 20” – 1
4. Endoscopic/ laproscopic Trolly -1
5. Gas Cylinder (CO2) 9 kg – 1
6. High pressure tubing - 1
7. Cidex Trya – 1
8. Formaline chamver 26” – 1
9. Servo stabilizer 1.0 KVA – 1
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 - 40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily , weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
engineer should be clearly spelt out
171
12. Equipment Specifications for Video Endoscope system upper GI
Pediatric Surgery
1 DESCRIPTION OF FUNCTION
1.1 System required for upper GI endoscopy for children
2 OPERATIONAL REQUIREMENTS
2.1 _ Videoprocessor with light source -- 1 no.
_ Gastro intestinal videoscope -- 2nos.
_ Duodenovideoscope -- 1 No.
_ Endoscope washer -- 1 No.
_ Accessories
_ Hardware for recording & archiving
3 TECHNICAL SPECIFICATIONS
3.1 1. PAL type video signal.
2. Controls for color adjustment, to enhancement and balance settings.
3. Controls to freeze images, enhance a portion of frozen image (zoom &
post-processing).
4. Patient and physician data input key board..
5. Operates on Halogen lamp/Xenon Lamp .
6. Emergency lamp.
7. Compatibility with the gastro scope, colonoscope and duodenoscope.
8. 15/17/19” LCD colour monitor with XGA resolution.
B. Forward Viewing Gastro Duodenoscope
1. Direction of view should be zero degree.
2. Minimum of 140 degree field view.
3. Range of observation at least from 5 mm to 90 mm.
4. Angulations of tip up and down of at least 180/180 degrees with right
and left movement of at least100/100 degrees.
5. Insertion tube diameter of less than 10 mm.
6. Distal end diameter of not more than 10.5 mm
7. Instrument channel of more than 2.5 mm
8. Working length of not less than 1000mm
Should be compatible with the video system specified.
9. PAL type video signal.
10. Controls for color adjustment, to enhancement and balance settings.
11. Controls to freeze images, enhance a portion of frozen image (zoom &
post-processing).
12. Patient and physician data input key board..
13. Operates on Halogen lamp/Xenon Lamp .
14. Emergency lamp.
15. Compatibility with the gastro scope, colonoscope and duodenoscope.
16. 15” LCD colour monitor with XGA resolution.
B. Forward Viewing Gastro Duodenoscope
9. Direction of view should be zero degree.
10. Minimum of 140 degree field view.
C. Three Chip Camera
1) High Definition Camera control unit
2) High definition Camera Head with 24 mm Coupler, 3.5 mtr cable
Specification and features
1. Only medical grade camera with the true digital output
2. High definition digital circuitry 3 chip camera
172
3. With 8 steps built-in digital enhancer
4. Electronic zooming
5. High definition features DIGITAL PROGRESSIVE SCANNING
TECHNOLOGY
6. Digital : Hi Definition (HD) Video 1289 x 1024 native resolution.
7. Small and ergonomic camera head for superior control.
8. Standard aspect ratio – To allow maximum exiting video equipment
9. Four button camera head design – control of six functions from the
camera head.
10. Multi specialty settings – user selectable specialty settings which
customize video output for the unique needs of different cases.
11. Signal to noise ratio > 70 db
12. Minimum illumination < 0.5 lux without gain enhancement
13. Control of the two peripheral accessories at camera head
14. One standard RGB output
15. 2 S VHS output
16. 2 S VHS (Video Composits) output
17. 2 Remote Output
18. Digital Image Capturing and Processing device should be able directly
record the images, take high resolution still snap shots, process the
videos, edit and should burn DVDs in high resolution.
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 - 40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 UPS of suitable rating with voltage regulation and spike protection for 60
minutes back up.
8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
173
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily , weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
engineer should be clearly spelt out
1 DESCRIPTION OF FUNCTION
1.1 For use in operation theater for neonates, infants and children
2 OPERATIONAL REQUIREMENTS
2.1 Electrically operated hydraulic operating Table for standard procedures of
surgeries
3 TECHNICAL SPECIFICATIONS
3.1 Length – 1800 mm Width – 400-600 mm
Hydraulic movements: -
1. Raising and lowering
Minimum height 650 mm
Maximum height 1100 mm
2. Lateral tilt – Left/right 28 degrees
3. Trendelenburg and reverse – 30 degree
4. Backrest section – 70 degrees up right, 30 degree down
5. Leg section – completely flat to right angle and detachable (for perineal
procedures)
6. Headrest - +25 0 / -45 0 (Detachable)
7. Kidney Bridge
8. Longitudinal displacement of the tabletop - 250 mm
Table should be C-Arm compatable
Tabletop should be X-Ray compatable
Mounted on Castor Wheels – so movement is smooth
Mechanical pedal brake – for firm and rigid locking
Brake release – Free to move
Radiolucent top and cassette carrier
Stainless steel base, body and accessories
For specialized procedures-Hand surgery, Femoral Tibial,and
interlock surgery
Lightweight and excellent manoeuvrability
Electro hydraulic pump in addition to the hydraulic foot pump
Five part, radiolucent tabletop
Remote hand control to activate the electro hydraulic pump
Table adjustments–High/ Low, Trendelenberg & lateral tilt
position,lithotomy position
174
4.3 Accessories : -
Anaesthetic frame
Padded side support
Intravenous arm board
Padded Shoulder Support
Wristlets
A pair of knee crutches
Foot rest with stainless top
Armrest
Body restraint strap
Wrist strap
Infusion rod
Attachment clamp
Head ring
Rack for accessories
Cassette carriers (X- ray)
Padded Lithotomy crutches with adjustable height (Two nos)
Additional Accessories one each
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%
5.2 The unit shall be capable of operating continuously in ambient temperature of
10 - 40deg C and relative humidity of 15-90%
6 POWER SUPPLY
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Rechargeable batteries and Battery charger 230V
8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine Preventive
Maintenance Support. as per manufacturer documentation in service/technical
manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instruction for daily, weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
engineer should be clearly spelt out
175
14. Equipment Specifications for ULTRASONIC ASPIRATOR FOR
PEDIATRIC SURGERY
1 DESCRIPTION OF FUNCTION
1.1 Ultrasonic aspirators use mechanical ultrasonic vibration and an
irrigation/suction system to fragment and remove soft tissue and high-watercontent
growths from various parts of the body.
2 OPERATIONAL REQUIREMENTS
2.1 The system should be quoted with the paediatric as well as adult hand pieces.
3 TECHNICAL SPECIFICATIONS
3.1 Surgical aspirator should be based on magneto-restriction or piezoelectric
technology.
3.2 The hand piece must be cooled if required to prevent overheating by coaxial
flow of water.
3.3 The hand pieces should be autoclavable and without need to dismantle for
autoclaving.
3.4 The vacuum pump should provide preferably the suction up to 700mm of Hg.
3.5 It should incorporate an Electro-surgical unit fitted on ultrasonic hand piece for
coagulation and cutting function.
3.6 The console unit should house control panel storage for foot switch, electrical
cords and self-contained suction apparatus.
3.7 The unit should include all necessary control preferably color-coded, which may
include amplitude, irrigation, aspiration and tissue select mode.
3.8 It should have safety features like optical signal for failed hand pieces and signal
for failed unit.
3.9 It should have on and off button.
3.10 It should have integral suction with vacuum pressure of-20 to -90 Kpa or 0.9 bar
in continuous low noise and digital display.
3.11 It should preferably have 2 liter capacity container of unbreakable material with
level sensor and anti-overflow system.
3.12 Hand piece should be light, preferable 20 -35 KHz and amplitude should be
>130 micrometers
3.13 The hand piece should be able to accommodate selection of tips for wide range
of applications.
3.14 The internal diameter of tips should range form 1.0 to 3.0mm.
3.15 The irrigation pump should be inbuilt in the unit, the irrigation output 0-
65ml/min.
3.16 All hand pieces/ instruments should be detachable.
176
8. Instrument connection cables- 2
9. Suction / irrigation tubing (5meter each), silicon twin tube-2.
10. Double set of cable and tubing clips- 10sets.
11. Metal puncture tube - 2
12. Sterilizing cassette with silicon mat and textile filter-2.
4.2 CONSUMABLES:
1. Textile filters for sterilizing cassette-10 pieces.
2. Suction/ Irrigation tubing (5 meter each) - 10 pieces.
3. Cable and tube clips - 5X 10 pieces.
4. Suction and Irrigation tubing, silicon twin tube (4.5 meters each) - 5
pieces
5. Disposable secretion bags 2 liters- 2 pieces.
6. Connection nipple, suction tube / secretion reservoir - 5 pieces.
7. Internal flushing tube - 5 pieces.
8. Protective cover-4 pieces.
5 ENVIRONMENTAL FACTORS
5.1 The unit shall be capable of being stored continuously in ambient temperature
of 0-50deg C and relative humidity of 15-90%
5.2 Thu unit shall be capable of operating in ambient temperature of 20-30 deg C
and relative humidity of less than 70%
5.3 Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility or should comply with 89/366/EEC;
EMC-directive.
6 POWER SUPPLY
6.1 Power input to be 220-240 VAC, 50/60 Hz fitted with Indian plug
6.2 Resettable over current breaker shall be fitted for protection
6.3 Voltage corrector/stabilizer of appropriate ratings meeting ISI Specifications.
(Input 160-260 V and output 220-240 V and 50 Hz)
6.4 Suitable UPS with maintenance free batteries for minimum one-hour back-up
should be supplied with the system.
8 DOCUMENTATION
8.1 User/Technical/Maintenance manuals to be supplied in English.
8.2 Certificate of calibration and inspection.
8.3 List of Equipments available for providing calibration and routine maintenance
support as per manufacturer documentation in service / technical manual.
8.4 List of important spare parts and accessories with their part number and
costing.
8.5 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job descriptin of the hospital technician and
company service engineer should be clearly spelt out.
177
8.6 Compliance Report to be submitted in a tabulated and point wise manner clearly
mentioning the page/para number of original catalogue/data sheet. Any point, if
not substantiated with authenticated catalogue/manual, will not be considered.
178
4. CYSTORESECTOSCOPE - FOR CHILDREN
A. Sheath with obturater with fixed irrigation channel with stopcock with
distal end insulated Size 11.5 Fr. ( One each) With instrument port capacity 5
Fr.
B. Adaptor (Bridge) ( one)
For examination with out instrument port
C. Working element with passive cutting action ( one)
D. Accessories
a. Electrodes
1. Coagulating electrode for resectoscope with telescope of 2.7 mm, angled
90 ° retrograde, Sickle shaped with distal ball – 6 No.s
2. Cutting electrode for resectoscope with telescope of 2.7mm.- 3 No.s
NOTE
1) The supplied instruments should have warranty period of 3 years
2) Annual Maintenance Contract facility to be provided after completion of
warranty period of 3 years
3). Supplier company will have to give training to doctors and staff of
Operation Theatre , regarding the handling and maintenance of the
instrument.
4) Supplier should have local service station to provide immediate repairs
of any Break down of the instruments and to provide the spare parts
and disposables articles, as and when required by the users of supplied
instruments.
5). The instrument should not be refurbished one and it should be fresh
supply from original manufacturer of the instruments
6) All the above instruments and equipments must be having relevant CE
certification as well as IEC certification., applicable to medical
instruments and
7). All eligible companies should be OEM and should have ISO 9001
certification or en 46001 certification. Additionally instruments should
have been tested in accordance with IEC 601-1 international. Apart
from this, companies having their own service centers in India will be
highly preferred.
179
4. Bronchoscope Sheath
Should have attachment (Channels) for anaesthesia ( Ventilation) and instruments and
optical prism light.
A. Bronchoscope sheath , size 6 , outer diameter 8.2 mm , inner diameter 7.5 mm ,
length :30 cm ( one )
B Bronchoscope sheath , size 5 , outer diameter 7.8 mm , inner diameter 7.1 mm ,
length :30 cm ( one )
C. Bronchoscope sheath , size 4.5 outer diameter 7.3 mm , inner diameter 6.6 mm ,
length :30 cm ( one )
D. Bronchoscope sheath , size 4 outer diameter 6.7mm ,inner diameter 6mm ,
length :30 cm ( one )
E. Bronchoscope sheath , size 3.7 outer diameter 6.4 mm , inner diameter 5.7 mm ,
length :30 cm ( one )
F. Bronchoscope sheath , size 3.5 outer diameter 6.4 mm , inner diameter 5.7 mm ,
length :30 cm ( one )
G. Bronchoscope sheath , size 4.0 outer diameter 6.7 mm , inner diameter 6.4 mm ,
length :26 cm ( one )
H. Bronchoscope sheath, size 3.7outer diameter 6.4 mm ,inner diameter 6.4 mm ,
length :26 cm (one)
I Bronchoscope sheath , size 3.5 outer diameter 5.7 mm , inner diameter 5.0 mm ,
length :26 cm (one)
J. Bronchoscope sheath , size 3.0 outer diameter 5.0 mm , inner diameter 4.3 mm ,
length :26 cm ( one )
K Bronchoscope sheath , size 3.5 outer diameter 5.7 mm ,inner diameter 5.0 mm ,
length :18.5cm( one )
L Bronchoscope sheath , size 3.0outer diameter 5.0 mm ,inner diameter 4.3 mm ,
length :18.5m (one)
M. Bronchoscope sheath , size 2.5 outer diameter 4.2 mm ,inner diameter 3.5 mm ,
length :18.5m ( one )
5. Optical forceps ( compatible with above mentioned telescopes and bronchoscope
sheaths)
A. Optical alligator forceps , 2x2 teeth , with spring action handle , for controlled
removal of flat foreign bodies ( such as coins) ;(two)
B. Optical forceps, with spring action handle for controlled removal of soft foreign
bodies ( such as peanuts) : ( two)
C. Optical alligator forceps, with forced controlled handle , for removal of hard
foreign bodies ( two)
6. Forceps( one each)
A. Forceps alligator, grasping , double action jaw , sheath diameter 1.5 mm ,
working length: 35 cm
B. Forceps alligator, grasping , double action jaw , sheath diameter 1.5 mm ,
working length: 35 cm , pointed serrated for coins and foreign bodies.
C. Forceps alligator , grasping double action jaw, sheath diasmeter 1.5 mm ,
working length 35 cm , pointed for peanuts and soft foreign bodies.
D. Biopsy Forceps 35 Cm
7. Sponge holder:
Spring handle, working length 35 cm ( one)
8. Rigid suction tube with rubber tip( one each)
A Rigid suction tube, straight length 35 cm, diameter: 3 mm
B Rigid suction tube, straight length 25 cm. diameter: 3 mm
9. Foreign body basket with rigid handle, working length 35 cm
10. Telescope bridge for fixed position between telescope and bronchoscope.
Compatible with above mentioned telescopes and bronchoscope sheaths ( Three)
11. Prosmatic light deflection with connection for fiber optic light cable, autoclave( Two)
12. Glass Window Plug ( Two)
13. Rubber Telescope Guide for use with telescopes or optical forceps (Two)
14. FLUVOG Adaptor with sliding glass window plug, sealing cap, notched lens and keyhole
opening , moveable ( two)
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15. Injection canula only. Leur lock outer diameter – 3.5 mm , for use with bronchoscope
tubes ( for positive pressure assisted ventilation ( (two) Injection canula only. Leur lock
outer diameter – 2.7 mm , for use with bronchoscope tubes ( for positive pressure
assisted ventilation ( (Two)
16. Instrument guide for suction catheter (Two)
17. Adaptor from bronchoscope to any type of pediatric respiration equipment ( Two)
18. Sealing plig for venti;ation attachment of bronchoscopes( Two)
19. Adjustable magnifier, swing – away type, autoclave (One)
20. Fiber optic light cable size 3.5mm, length 180 cm (Two)
21. Cold light fountain twin bulb Halogen 150 watts Power supply
220 VAC, 50 Hz. ( One)
Note
1. The supplied instruments should have warranty period of 3 years.
2. Annual maintenance contract (AMC) facility to be provided after completion of warranty
period of 3 years.
3. Supplier company will have to give training to the doctors and the staff of operation
theatre, regarding the handling and maintenance of the instrument on site.
4. Supplier should have local service station to provide immediate repairs of any
breakdown of the instruments and to provide the spare parts and disposables articles ,
as and when required by the users of the supplied instruments.
5. All theabove instruments and equipments must be having relevant CE certification as
well as IEC certification , applicable to Medical Instruments and equipments.
6. All eligible companies should be an OEM ANS SHOULD ALSO HAVE iso 9001 certification
or EN 46001 certification . Additionally instruments should have been tested in
accordance with IEC 601 -1 international.
Apart from the companies having their own service centers in India will be highly
preferred.
181
7. All eligible companies should be OEM and should have ISO 9001 certification or
en 46001 certification. Additionally instruments should have been tested in
accordance with IEC 601-1 international. Apart from this, companies having
their own service centers in India will be highly preferred.
18. PATIENT WARMING DEVICE FOR O.Ts (Adults & Paed.) THERMAL
MATTRESS
Should be suitable for intra operative applications
Should consists of active warming arm-cum shoulder section pair of leg segments and
1 double segments to cover the entire body
Size double segment : (60-62)cm X(80-85) cm Arm & shoulder section : (35-40) cm X
(175-180) cm
Leg segment : (80-85) cm
Each double segment & arm cum shoulder segment should have two temperature
sensors each for precise temperature control
Double segment & arm cum shoulder segment should be divided in two sections
capable of being switched ON and OFF independently depending upon the nature of
surgery and condition of patient
Should have a control unit to regulate warmth to every area precisely by use of
carbon fibers
Control unit should be capable of warming at least three segments at a time
Should offer precise digital temperature control with selectable temperature range of
30 to 42 degree C in steps of 0.5 degree C
Control panel should display intended and actual temperature
Should have safety features such as automatic check. Precise temperature control
between warming system and patient, auto stop on detecting any problem
Should have non latex anti-bacterially coated , blood and fluid resistant covers
Covers should be washable and replaceable
The control unit should be light weight not more than 2.5 kg, small in size
(200X120X230mm approx) and easily attachable to IV rod/OT table with fixing claw
Should have low energy consumption and noiseless operation
182
Resuscitation. This unit fulfils basic need of resuscitation and hence life-saving
action can be taken without delay
2. TECHNICAL SPECIFICATIONS
Should be available of :-
Power Source230 +/- 10% volts, 50Hz. Control Method Proportionate Power Control
Light Source
60Watts bulb to Examine babies. Power Consumption 850 Watts minimum.
Acrylic Tray with Foam mattress. Trays & structure fabrication in Stainless steel. IV pole
& Facility to take X-ray. Head up / down facility (continuous variable). 2 Drawer storage
cabinets mounted on heavy duty castors
3. STOP WATCH
Additional facility provided to note down timings during monitoring various vital signs
of baby e.g. Temp, Heart Rate and Respiration Rate.
4. ALARMS :
Skin + 1 C HI Air + 1.5 CHI Skin - 1 C LO Air - 3 CLO Skin > 38 C OVER Air > 39 COVER
Skin / Air Sensor Failure FAIL Heating Failure POWER FAILURE Audio-visual HEAT OFF
Resolution : 0.1 C SAFETY CUTOFF Accuracy : 0.1 C Skin > 38 C Skin > 39 C
5. RESUSCITATION FACILITY
To monitor pressure of Oxygen delivered to baby through Manual Resuscitator bag.
OXYGEN ADMINISTRATION: Oxygen Flow Control facility with Flow meter (0 to 15 Lt /
min), Oxygen Pressure adjustment valve, Humidifier Bottle, Facility to keep Oxygen
Cylinder, Connecting Hose for wall outlet. Silicon Autoclavable Resuscitation Bag with 00
and 01 size of masks. SLOW SUCTION: This is a specially designed electrically operated
slow suction. Apart from others, it is non-motorized slow suction. The Suction pressure
can be adjusted as per requirement ( 0 - 110 mm Hg ) . LARYNGOSCOPE: with Penlight
Handle & 0 and 1 Miller Blades.
8. RESUSCITATION CRIB
Should be Provides the Mobile aid needed for airway management and mounted on
mobile crib for easy manoevouring and fast access during resuscitation and also
available following functions:- Slow Suction ,Oxygen Flow control with Humidication
,Inline Manometer to monitor pressure delivered to baby during Bag-n-Mask
resuscitation. The mobility allows use of the Resuscitation Crib on multiple warmers or
incubators for use in Labour, Delivery or Neonatal Intensive Care areas.
183
9. SERVO CONTROL SYSTEM TO MAINTAIN AN OPTIMUM SKIN
TEMPERATURE
Should be available this system to detects minute variation in skin temperature with a
precision temperature with a precision temperature probe attached to the infant’s
abdomen and maintains an optimum environmental temperature by calculating an
accurate balance between the infant’s skin temperature and cradle temperature.
Heating box is swivel type to take X-ray. Full cradle length Heaters to avoid cold and hot
zone in cradle, and this system provides uniform heat over entire mattress. Spark proof
Quartz or Ceramic Heating System. 600watt Quartz infrared Radiant Heater provides
optimal environment.
12. CPAP
Complete solution to all difficulties faced in Bag - n - mask type resuscitation. Peak
Inspiratory Pressure (PIP) control valve to adjust the maximum Inspiratory pressure delivered to
baby. Positive End Expiratory Pressure ( PEEP ) control valve to maintain minimum positive
pressure at the end of expiration to keep the lungs inflated. Overall control over system by
setting Maximum Pressure Relief to the system.
Inspection by consignee.
184
EQUIPMENT RADIOLOGY -13
1. IITV system
with image memory 9” triple field full wave rectified x-ray generator electronically
operated control unit with touch control below mentioned specification fluoroscopy MA
0.3 to 5ma KV 40 to 100KV auto dose rate control 40 to 100kv fluoroscopy timer digital
fluoroscopic timer with auto exposure cut off after pulsed fluoroscopic is provided
Radiography KV 40 to 100KV MAs 01 to 200 mAs digital display fluoroscopy KV, mA, timer
& radiography mAs, image orientation horizontal and vertical image reversal is performed
both from control panel and monitor image rotation +/- 270 deg image rotation is also
performed both from control panel and monitor tube used imported fully lead linked
double focus stationary anode x-ray tube small focus 0.6mm x 0.6mm for fluoroscopy large
focus 1.8mm x 1.8mm for radiography sleek designed tube head power input single phase
230 volts, 15 Amps specification of IITV latest series 9” image intensifier with high
resolution input phosphor screen with thin metal input high gain more than 180 center
resolution 52 lines/cm TV camera CCD camera single unit type with low input high
resolution CCD specially designed to operate with image Monitor 17” monitor high
resolution type 15 MHZ frequency response with image reversal capabilities Trolley mobile
trolley height 130cm swivel type with lock C-Arm stand the C-arm stand in ruggedly
designed with all movements self balanced easy maneuverability manual locking wheels are
connected through chain prote tive cable guard for floor wheels focus II distance 900mm
motorized up-down travel 430mm horizontal travel 220mm orbital range 125deg. Panning
+12.05deg detachable cassette holder for 8”x10” of 10”x12” film Image memory system
resolution 512x512 pixel, pixels depth 250 grey levels (8bit) sampling rate 12.5MHz video
bandwidth (-3db) 4.5MHz video in/out CCIR standard (625 lines / 50 Hz) acquisition time
real time (1/25th of a second) averaging facility 2/4/8/16 frames real time (1/25 th of a 1)
sweep reversal black & white Power input 230v ac, 50Hz +/- 10% FS-10-PC memory 32
image memory with In built computer transfer facility to store the image hence very high
numbers of images can be stored the dual monitor is supplied along with the system 1 st
monitor display last image hold and 2 monitor display memory images 4/8/16/32/64/256
nd
185
Requirement for a sturdy, fully digital ultrasound system for
whole body scanning with latest state of art technology and
softwares for fast, accurate and wide ranging applications in a multi
specialty 250 bedded hospital with 100-150 patients work load per
day.
186
11. Large image storage facility through 80 GB (or expandable)
for raw data storage in main machine or in additional PC for
recall and reanalysis, non perishable on switching off.
12. Extensive raw and post processing application softwares for
measurements /calculations/trend/graph/for general radiology/
abdominal/ vascular/ chest/obg/ortho/ msk/small parts/fetal
echo Cardiography etc. to provide details. (Full details should
be provided.)
PERIPHERALS:
1. Inbuilt CD read/write.
2. Compatible laser (toner based) printer-scanner-copier.
3. DICOM/Teleradiology/Pacs compatible image management
software including PNDT and system (PC based work station)
4. Proper user manual, text books and references for software
applications.
187
Final image quality, ergonomics of the machine usage , fast
performance matrix, highest frequency achievable, 2D /3D/4D, reporting
softwares, pre and post prog will have to be demonstrated on TEC on
phantoms and patients before final purchase.
188
3.TECHNICAL SPECIFICATIONS FOR COLOR DOPPLER
ECHOCARDIOGRAPHY SYSTEM
189
3.6 Steerable PW/CW in all Phased Array probes.
3.7 High definition acoustic zoom for enlarging sections of 2D and Color flow
images with
more acoustic information for greater clarity and detail while maintaining
an optimal frame rate.
3.8 Modes - 2D, M-Mode, Steerable PW/CW Doppler, Color Doppler, and High
Definition Color flow with capability of automatically picking up color flow
as a function of focal depth
3.9 Monitor should be 15" or more, high resolution color Monitor.
Tilt and Swivel monitor should be able to view in all angles and all light
conditions.
3.1 Color Flow Imaging for
0 a) Increased lateral & spatial resolution.
b) Detection of even subtle areas of turbulence, displaying a more
physiological blood flow appearance without loss of frame rate.
c) Color flow with capability of automatically picking up color flow as a
function of
focal depth
3.1 Tissue Colorization (B-Color) for improved contrast resolution
1
3.1 Application software for Adult, Pediatric, Fetal and Peripheral Vascular and
2 Transesophageal applications. (All application package should be built into
the system)
3.1 Cine loop memory- more than 120MB of memory.
3 a. High Frame rate review for better clarity of playback images study in
slow motion.
b. Quad loop with memory for pre and post image comparison of any
procedure.
c. Memory- 256 frames or more in quad loop. M Mode & Doppler Scroll
Memory-40 seconds or more.
d. Frame grabber facility for post analysis.
3.1 Various maps for pre and post processing.
4
3.1 ECG trigger facility.
5
3.1 User defined system and application presets for multi-user department.
6
3.1 Minimum 4.8 GB optical disc drive for image storage and retrieval.
7 (standard with system)
3.1 Dedicated integrated dynamic stress echo package for flexible user
8 defined protocols with stacked sub loops facility and contrast stress
protocol.
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2 editing of complete patient studies.
3.2 Facility of Real time perfusion studies
3
3.2 SYSTEM PERIPHERALS should include
4 a. CD Writer with calculation facility on playback.
b. Color Video Printer.
c. B/W Thermal Printer.
3.2 Colour M-Mode
5
* Acoustic densitometry is unique nomenclature of Philips Medical System and
hence is not being used.
S.N System Configuration Accessories, spares and consumables
.
4.1 Color Doppler System with all application packages
Quad loop for serial studies with High frame rate review.
Harmonic imaging capability in all modes. (Tissue, Contrast, Anglo)
Integrated Stress Echo Package Digital Storage and Retrieval- 01
4.2 1.0-3.0 MHz Adult Cardiac probe Electronics Phased Array probe.- 01 ea
4.3 3.0-11.0 MHz Electronics Phased Array Probe for Vascular applications- 01
ea
4.4 Multiplane TEE Probe- (Optional)
4-8 MHz for Adult as well as Paediatric echocardiography.
4.5 5.0-10 MHz Electronic phased array probe for Paediatric cardiology.
(OPTIONAL
4.6 DVD/CD Recorder with 100 CDs and 100 DVDs
4.7 Color Printer. -01
4.8 B/W Video Thermal Printer -01
4.9 Colour Print Paper- 500 sheets
4.1 B/W Thermal Paper - 10 rolls
0
4.1 ECG Cable - 02
1
4.1 MO Disc - 10
2
The system should contains all the above accessories in Integrated or as
separate accessories..
S.N Environmental factors
.
5.1 The unit shall be capable of operating continuously in ambient
temperature of 300 C and relative humidity of 80%
5.2 Pre Requsites should be clearly spelt out in terms of room requirements..
S.N Power supply
191
.
6.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
6.2 Resettable overcurrent breaker shall be fitted for protection
6.3 Suitable Servo controlled Stabilizer/CVT
6.4 UPS of suitable rating conforming to IS-302 shall be supplied . Servo
stabilizer is not required if the UPS has voltage correction facility.
S.N Standards and safety
.
7.1 Should be FDA or CE approaved product
7.2 Electrical safety conforms to standards for electrical safety IEC-60601 / IS-
13450
7.3 The product shall comply to IEC 60601-2-37 ed1: Medical Electrical
Equipment - Part 2-37: Particular Requirements for the Safety of Ultrasonic
Medical Diagnostic and Monitoring Equipment
7.4 Type of protection againstelectric shocks -- Class I
Degree of protection against
electric shocks for ultrasound probes Type "BF"
For ECG electrodes Type 'CF"
7.5 The manufacturer should have ISO certification for quality standards.
S.N Documentation
.
8.1 User manual in English
8.2 Service manual in English
8.3 List of important spare parts and accessories with their part number and
costing.
8.4 Certificate of calibration and inspection from factory.
8.5 Log book with instruction for daily , weekly, monthly and quarterly
maintenance checklist.
The job description of the hospital technician and company service
engineer should be clearly spelt out
8.6 List of equipments available for calibration and preventive maintenance as
laid down in the Technical/Service Manual.
192
4. TECHNICAL SPECIFICATIONS (GENERAL) FOR THE PROCUREMENT
OF 500 MA DIAGNOSTIC X-RAY MACHINE.
193
5.TECHNICAL SPECIFICATIONS 300MA X-RAY MACHINE
X-RAY MACHINE 300mA. 125 KVP Full Wave Solid State Silicon Rectified X-
ray Generator for Radiography suitable for single Tube
Operation as per IS:7620 with latest amendments.
TIMER The exposure timer should be digital & from 0.02 sec to 5
sec.
CONTROL Consisting of On & Off Switches, with Voltmeter, MA meter,
Quick trip-overload circuit breaker (Automatic safety system
to block unwanted exposure factors beyond Tube Rating),
Voltage Compensator, Major & Minor KV selector, Tube
overload indicator provided, Space charge compensator,
technique selector. Digital Display of KVP, & mAs, Anode
braking Device. Electronic overload for protection of tube
H.V. Cables & H.T. Tank. Ready & X-Ray Switch on
Control.
Static balancer 30 KVA capable of converting 3-phase in range 365-400
VAC with 0.2 ohms resistance at 50-60Hz to single phase
230 VAC/50Hz
HV TRANSFORMER Compact Heavy Duty Transformer comprising HV Silicon
Rectifiers, HT Transformer, Filament Transformer, bushings
all immersed in oil.
ACCESSORIES Hand Switch with Flexible long cord enables the operator to
keep away from the Radiation area during exposure.
- Aluminum Filter.
- Light Beam Diaphragm.
POWER SUPPLY 440V + 10% V AC, 50 Hz, Three Phase -
REQUIREMENT
TUBE UNIT One No. 20/40 Rotating Anode Tube (BEL / TOSHIBA or
equivalent) with Dual Focus (Large & Small).
HV CABLE One Pair of 10 meter High Voltage Cables :
Sleevings - Straight.
STAND Floor to Ceiling Stand & with Counter Balanced Tube Head
(Rotatable+180 Degree), 360 Degree Rotatable; mounted on
Floor Ceiling Rails for convenient movements.
It should have all necessary locks.
The column should be light in weight.
Protection for the rope failure should be provided with the
column stand.
TABLE 5 Position Table Hand tilt; 15 Degree trendelenburg to
vertical, Motorised Bucky consisting of 8:1, 103 lines/inch
Imported Grid Size 17 1/4" X 18 7/8"; Stainless Steel Cassette
Tray; Compression Band and Foot Rest.
VERTICAL BUCKY Vertical Bucky Stand with moving Grid of Ratio 8:1, 103
lines/inch. The Bucky moves up & down & are equipped
with stainless steel cassette. This stand is floor-mounted type
& can accommodate cassettes up to 14" X 17".
194
6.TECHNICAL SPECIFICATIONS 100MA X-RAY MACHINE
X – RAY GENERATOR 100mA – 125 KV High frequencies X- Ray Generator with
Rotating Anode X-Ray Tube & 10 KW X-ray Generator.
FREQUENCY 20 kHz & Above
MAX. MA OUTPUT 100 mA
mAs RANGE 1 to 200mAs.
KV RANGE 40 to 125 KVP
195
7.Main Technical Parameter:-
Output 60mA-100kV
Radiographic kv 30 to 100 kV
Fluoro mA 0 - 3 mA
6 KVA 1 Phase
196
Special/optional features:-
197
EQUIPMENT VENTILLATOR-14
1. Equipment Specifications for Ventilator-High End (I.C.U)
1 Description of Function
Serial Name
no
1.1 ICU ventilators provide artificial respiratory support to the critical patients in the
Intensive Care Units.
2 Operational Requirements
Serial Name
no
2.1 Microprocessor Controlled ventilator with integrated facility for
Ventilation monitoring suitable for New born to adult ventilation.
2.2 Demonstration of the equipment is a must.
3. Recomendde for health facilty like distric hospital and medical colleges.
4 Technical Specifications
Serial Name
No
3.1 Standard hinged arm holder for holding the circuit
3.2 Colored TFT screen, 12 Inch or more
3.3 Facility to measure and display
a) End tidal CO2 with capnography.
b) 3 waves- Pressure and Time, Volume and Time and Flow and Time.
c) 3 loops- P-V, F-V, P-F with facility of saving of 3 Loops for reference.
d) Graphic display to have automatic scaling facility for waves
e) Status indicator for Ventilator mode, Battery life, patient data, alarm settings,
clock etc
Trending facility for 72 hours with minimum 5 minutes resolution
for recent 24 hours
3.4 Automatic compliance & Leakage compensation for circuit and ET tube
Following settings for all age groups.
a) Tidal Volume
b) Pressure (insp)
c) Pressure Ramp
d) Respiratory Rate
e) SIMV Respiratory Rate
f) CPAP/PEEP
g) Pressure support
h) FIO2
i) Pause Time
3.5 j) Pressure & Flow Trigger
Monitoring of the following parameters
a) Airway Pressure (Peak & Mean)
b) Tidal volume (Inspired & Expired)
c) Minute volume (Inspired and Expired)
d) Spontaneous Minute Volume
e) Total Frequency
f) FIO2 dynamic
g) Intrinsic PEEP and PEEPi Volume
h) Plateau Pressure
i) Resistance & Compliance
j) Use selector Alarms for all measured & monitored parameters
3.6 Modes of ventilation
a) Volume controlled
b) Pressure Controlled
c) Pressure Support
d) SIMV (Pressure Control and volume control) with pressure support
e) CPAP/PEEP
198
f) Inverse Ratio Ventilation
g) Advanced mode like pressure controlled volume guaranteed
h) Non Invasive ventilation
i) APRV
Apnea /backup ventilation
3.7 Expiratory block should be autoclavable and no routine calibration required
Should have the ability to calculate / Procedure
a. Intrinsic Peep & Intrinsic PEEP Volume
b. Occlusion Pressure
c. Spontaneous Breathing trial
d. Facility to calculate lower and upper inflection point
Nebuliser with capability to deliver particle size of < 3 micron & to
be used in both Off and On line
Automatic Patient Detection facility preferable
3.8 Medical Air Compressor. (Optional)
a) Stand-alone Medical Air compressor
b) Snap fit with the Ventilator module to provide an oil free Medical air.
c) Peak output flow should be minimum 160 LPM.
d) Air quality should comply with ISO compressed air purity class.
e) Medical Air Compressor should automatically activate in the
event of wall air supply loss.
f) Replacement of internal filters should be performed without
removing the compressor
g) Should have washable air filter.
3.9 Technical Specifications for reusable face mask & nasal mask.
3.10 Reusable face & nasal mask with textured dual flap silicone cushion flap for easy fit.
Removable forehead support and pad to match the angle of patient’s forehead
3.11 Stability Selector for easy fit and angle.
Ball & Socket headgear attachments.
Should be autoclavable.
Battery back up for minimum 1 hour
3.12 RS 323C interface for communications with networked devices.
3.13 Automatic patient detection facility preferable.
3.14
4 System Configuration Accessories, spares and consumables
Serial Name
no
6 Power Supply
Serial Name
no
6.1 Power input to be 220-240VAC, 50Hz
6.2 Suitable Servo controlled Stabilizer/CVT
6.3 Resettable overcurrent breaker shall be fitted for protection
Suitable UPS with maintenance free batteries for minimum onehour
6.4 back up should be supplied with the system.
199
Should have local service facility .The service provider should have the necessary
7.7 equipments recommended by the manufacturer to carry out preventive
7.8 maintenance test as per guidelines provided in the service/maintenance manual.
Comprehensive warranty for 5 years and provision of AMC for next 5 years.
Back to back warranty to be taken by the supplier from the principal to supply
spares for a minimum period 10 years.
8 Documentation
Serial Name
no
8.1 Certificate of calibration and inspection from factory.
8.2 List of Equipments available for providing calibration and routine maintenance
support as per manufacturer documentation in service / technical manual.
8.3 User Manual in English
8.4 Service manual in English
8.5 Log book with instructions for daily, weekly, monthly and quarterly maintenance
checklist. The job description of the hospital technician and company service
8.6 engineer should be clearly spelt out.
8.7 List of important spare parts and accessories with their part number and costing.
Compliance Report to be submitted in a tabulated and point wise manner clearly
mentioning the page/para number of original catalogue/data sheet.Any point ,if not
8.8 substantiated with authenticated catalogue/manual, will not be considered.
8.9 Must submit user list and performance report within last 5 years from major
hospitals.
Back to back comprehensive warranty to be taken by the supplier from the principal
to supply spares for minimum 10 years.
2. Equipment Specifications for Transport Monitor
1 Description of Function
Serial Name
no
1.1 Transport Monitor is required to monitor vital parameters of patients during
transportation to and from OT; Emergency;Trauma ambulances etc.
2 Operational Requirements
Serial Name
no
2.1 Transport monitor should be portable and lightweight and should monitor vital
parameters of patients.
2.2 Capability of storage of patient data and printing of patient reports.
2.3 Capability to integrate with the HIS and transfer the data through LAN / Wireless
LAN to any other monitoring room / doctors desk. Should be HL-7 compatible for
transmitting and receiving datato/fro LAN/HIS (OPTIONAL)
2.4 Demonstration of the quoted equipment is a must
3 Technical Specifications
Serial Name
no
3.1 Portable and Light weight preferably <10kg
3.2 12 inch multi color TFT display
3.3 Monitoring parameters: - ECG, respiration, NIBP, SaO2 and temperature
3.4 Digital and 4 waves / traces display
3.5 Monitor should have audible and visual alarms capability. Alarms should have three
distinct audible alarm tones to distinguish alarm levels. Also monitor should permit
automatic viewing of alarming parameter waveform and numeric from any bedside
in alarm as and when connected in a network.
3.6 Trends should be automatically stored for at least 24 hours in at least one-minute
3.7 intervals. Numeric monitored data trend shall be viewable and recordable in a
patient chart type format in at least 1, 5, 15, 60 minutes intervals.
3.8 Convenient handle for carrying the same
3.9 Able to fix with bed/trolley.
200
NETWORKING AND REMOTE ACCESS (Optional)
1.Remote access of patient data -should have facility of accessing patient data
including waveforms and numeric remotely in Hospital or at Consultants residence
through hardwired LAN connection or through modem.
2.Should also offer viewing station for viewing this data as optional item.
3.Should be upgradeable.
4.Should be able to review DICOM images from PACS. On the bedside or the central
station.
5. Web browsing facility to review each networked monitors data through hospital
LAN via office PC in Hospital LAN network and/or through dial up facility from
remote location.
6. To provide HL 7 compatible server for sending information from the monitoring
network to Hospital Information System, Laboratory information etc for integration
of various information
201
8.2 Service manual in English
8.3 List of important spare parts and accessories with their part number and costing.
8.4 Certificate of Calibration and inspection from the factory
8.5 Log book with instruction for daily, weekly, monthly and quarterly maintenance
checklist.
8.6 The job description of the hospital technician and company service engineer should
be clearly spelt out
8.7 List of Equipments available for providing calibration and routine maintenance
support as per manufacturer documentation in service / technical manual.
Must submit user list and performance report within last 5 years from major
hospitals.
202
patient cable assembly 1no, spo2 sensor 1no, adult NIBP cuff 1mo, disposable
electrodes 30pcs, user manual 1no
203
MESUREMENTS
Peak airway pressure, means airwaypressure, and peep Pplateau by tele-
inspiratory pause
Auto – peep by tele expiratory pause Static compliance Inspiratory resistance
Proximal pressure and flow (in addition toventilator based measurements)
Tidal volume – expiratory
Minute volume – expiratory
Breathing rate – Ti/Ttot FIO2
Trends for 72 hours
Vt, Vmin, RR, pPeak, pMean, peep Pplateau auto peep Cstat, Rinsp
Alarms
Pmin, Pmax, Fio2 min. Fio2 max, Vtmin, max, vminute min, vminute max Patient
disconnect, gas supply power supply, Apnea ventilation, Automatic alarms settings,
Alarms memory, Alarms history
Graphics
Reel time pressure curves with adjustable time scales
Real time flow curves with adjustable time scales
Special Graphics
Pressure/volume loops with adjustable curves scales and freezing and calculation
facilities, flow/volume loops with adjustable curves scales and freezing and
calculation facilities, pressure flow loops with adjustable curves scales and freezing
and calculation facilities
OTHERS
Nebulization / Suction Control / Automatic control and calibration Back-up
ventilation / User’s configuration menu Optional
MDV Screen
Two configuration screens both ventilation and monitoring dedicated screens are
designed to offer a more rational approach of settings. Designed to offer a more rational
approach of settings Further more, to provide an acute analysis, HOURS 4 is easily
equipped with its special ventilation monitor “MDV”
Air Supply Unit for Respirator Horus 4
Humidifier MR 810 with Adult Chamber
Peadiatric chamber
EC humidifier with adult chamber
5. Anaesthesia Ventilator
Power Input : 220V 50Hz
Tidal Volume : 100 to 1200ml
Sigh : 1.5 times Tidal Volume
Type : Volume, time cycled Ventilator electrically operated,
Pneumatic engine I/E Ratio : Variable from 1:1 to 1:3
Safety Pressure : Fixed (60m Bar)
Frequency : 8 to 40 cycles per min.
Pressure indicator : LED bar graph display
Pneumatic requirement : 3-bar pressure
6. Transport Ventilator.
Peak flow rate in CMV-ACMV – 100 L/min
204
Peak flow rate in PS-PEEP - 130 L/min
Gas consumption - 1 L/min
Pneumatic supply - 2.8 to 6 bar
Internal electrical power supply – NiCd batteries pack
Battery life - 10 h
Charging time - 10 h
Mains power supply Input - 230V / 50 Hz
Output - 15V / 6 W
Dimensions (L X H X D) - 250 X 210 X170 mm
Weight - 5.0kgs.
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