Autoclave Getidy

CONTENTS
Sheet for rapid use....................................................................................... .............................. ..Enclosure

Chap.1-Guarantee
1.1-Guarantee................................................................................... .................................. Page04
1.2-Certificate of guarantee............................................................ ...................................... Page04
Chap.2-Introduction....................................................................................... .............................. ...Page05
2.1-Reference standards..................................................................... .............................. ...Page05
2.2-Staff requirements......................................................................... .............................. ..Page05
2.3-Using and storing the manul......................................................... ................................ ...Page05
2.4-Reading the manual:symbols and conventions............................... ................................ ..Page05
2.5-How to obtain a new copy of the manual......................................... ................................ ..Page06
Chap.3-Safety................................................................................................................................Page 07
3.1-General safety warnings................................................................ ............................... ..Page07
3.2-Intended use............................................................................... ................................ ...Page08
3.3-Safety devices............................................................................ ................................ ...Page09
3.4-Residue risks.............................................................................. ................................ ...Page12
3.5-Safety signs on the unit............................................................... ................................ ....Page13
3.6-Personal protective equipment..................................................... ................................ ...Page13
Chap.4-Receipt and handling........................................................................ ................................ ...Page13
4.1-Weight and dimensions of packing.................................................... .............................. ..Page13
4.2-Receipt and handling.......................................................................................................Page14
4.3-Description of contents....................................................................................................Page14
4.3.1-Optional devices...........................................................................................................Page14
Chap.5-Description of unit................................................................................................................Page15
5.1-Description of unit............................................................................................................Page15
5.1.1-Front elements.............................................................................................................Page15
5.1.2-Rear elements..............................................................................................................Page16
5.1.3-Upper elements............................................................................................................Page17
5.1.4-Description of control panel....................................................................................................Page17
5.2-Overall space required................................................................................................ ....Page18
Page 1 of 62
5.3-Technical date and noise..................................................................................................Page18
5.3.1-Rating plate.................................................................................................................Page20
5.3.2-Noise level...................................................................................................................Page21
5.4-External printer........................................................................................................... . ..Page21
Chap.6-Installation and first start-up.................................................................................................Page22
6.1-Work environment:positioning..........................................................................................Page22
6.2-Installing the unit.............................................................................................................Page23
6.3-Electrical connections.................................................................................................... .Page24
6.4-First start-up...................................................................................................................Page25
6.5-How to use the control panel.............................................................................................Page25
6.6-Tanks:instructions for filling and draining...........................................................................Page26
Chap.7-Operation...........................................................................................................................Page28
7.1-Prepare work before operation........................................................................................ .Page28
7.1.1-Trun on........................................................................................................................Page28
7.1.2-Set time......................................................................................................................Page28
7.1.3-load the material......................................................................................................... .Page28
7.2-Selecting a sterilization cycle...........................................................................................Page29
7.3-Set user-definned.......................................................................................................... .Page30
7.4-Test program.................................................................................................................. Page30
7.4.1-Vacuum test.................................................................................................................Page31
7.4.2-Cleaning......................................................................................................................Page32
7.5-System set......................................................................................................................Page32
7.5.1-Time set...................................................................................................................... Page32
7.5.2-User input....................................................................................................................Page33
7.5.3-Printer set....................................................................................................................Page33
7.6-Record...........................................................................................................................Page34
7.7-Information.....................................................................................................................Page34
7.8-Three times pre-vacuum sterilization process graphic ...................................................... ..Page35
7.9-One times pre-vacuum sterilization process graphic ..........................................................Page36
7.10-Abnormal Exiting.............................................................................................................Page37
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7.11-Some indications on screen....................................................................................... .. ..Page38
Chap.8-Maintenance..................................................................................................................... .Page40
8.1-Safety warnings...............................................................................................................Page40
8.2-Routine maintenance...................................................................................................... .Page40
8.2.1-Periodic maintenance....................................................................................................Page44
8.3-Extraordinary maintence.................................................................................................. Page45
8.3.1-Rusting........................................................................................................................ Page47
Chap.9-Scrapping.......................................................................................................................... Page47
9.1-Scrapping instructions......................................................................................................Page47
9.2-Resale............................................................................................................................Page47
APPENDIX 1..................................................................................................................................Page48
Preparing the instruments for sterilization................................................................................Page48
APPENDIX 2..................................................................................................................................Page49
Packing................................................................................................................................ Page49
APPENDIX 3..................................................................................................................................Page50
Positioning the load............................................................................................................... Page50
APPENDIX 4..................................................................................................................................Page51
Unloading and preserving the sterilized instruments................................................................. Page51
APPENDIX 5..................................................................................................................................Page52
Description of programs..........................................................................................................Page52
APPENDIX 6..................................................................................................................................Page55
Description of tests.................................................................................................................Page55
APPENDIX 7..................................................................................................................................Page57
Validating thecycles................................................................................................................Page57
APPENDIX 8..................................................................................................................................Page58
Quality of process water..........................................................................................................Page58
APPENDIX 9..................................................................................................................................Page59
Troubleshooting......................................................................................................................Page59
APPENDIX 10
Components graph of whole machine ..........................................................................................Page61
APPENDIX 11
Hyhranic Circuit......................................................................................................................Page62
Page 3 of 62
1. Guarantee
1.1 GUARANTEE
Getidy M.I.Co.,ltd. guarantees the quality of its equipment, if used in accordance with the instructions contained in this
manual, according to the conditions indicated in the Certificate of Guarantee (see chap. 1.2).
ATTENTION: the CUSTOMER must fill in all parts of the COUPON in the certificate of guarantee and send
i it to Getidy M.I.Co.,ltd.
The guarantee period starts from the delivery date of the unit to the customer; this date is confirmed by returning the
guarantee slip correctly, duly filled in and signed. In the case of dispute, the date indicated on the purchase invoice, showing
the serial number of the unit, will be considered as valid.
1.2 CERTIFICATE OF GUARANTEE (facsimile)
CERTIFICATE OF GUARANTEE GUARANTEE
Facsimile
The zhejiang getidy medical instrument co.,ltd will
Model:
give one year warranty time under the operator use
Serial Number: the device according the instruction manual,but the
zhejiang getidy medical instrument co.ltd declines
Purchase date: all liability for accidents to people or damage or
Agent Name malfunctions of the unit if the instruction manual is
not be observed,and this after-sales service will be
Add paid.
Tel: Fax:
ZHEJIANG GETIDY MEDICAL INSTRUMENT CO.,LTD
User information Add:NO. 9 Weisan West Road,Hardware Machine
Industrial Area,Tongqin,Wuyi,Zhejiang,China.
Clinic Name Tel:0086-579-87707205 87707499 87707488
Fax:0086-579-87707467 P.C:321201
Add E-mail:getidy@getidy.com
Web:www.Getidy.com
Professiond operator
Tel/Fax/E-Mail:
Agent:
Advice
Page 4 of 62
2. Introduction
2.1 REFERENCE STANDARDS
JQ-A series Steam sterilizer
The saturated steam sterilizer complies with the essential requirements of Council Directives:
Medical devices 93/42/CEE of 14/06/93, class II A - 0197 .
It also complies with the national standards in their harmonized versions:
EN 13060,EN 61010-1,EN 61010-2-041,EN 61326,EN ISO 14971,EN 60601-1-4
Boiler
It also complies with the essential requirements of Council Directives:
Pressure vessels 97/23/CE of 29/05/1997 - Category II-D1- 0197.
The boiler complies with the following standards: EN 13445:2002.
2.2 STAFF REQUIREMENTS

The staff authorized to use and service the equipment must possess the following requirements:
--sufficient general culture to understand the contents of this manual;
--knowledge of the machine and its place of installation;
--knowledge of health, accident prevention and technical regulations.
The main figures who operate and service the unit are shown below.
The OPERATOR is the person who physically uses the unit for the purposes for which it has been designed.
The RESPONSIBLE AUTHORITY is the person or group responsible for the use and ordinary maintenance of the unit and for
operator training.
The responsible authority is legally responsible for the installation, operation and use of the unit.
2.3 USING AND STORING THE MANUAL

This manual is an integral part of the product and must be kept near the unit for quick and easy consultation.
This manual contains instructions for:
--correct installation;
Page 5 of 62
--the safe and efficient operation of the unit;
--continuous and regular maintenance.
The unit must be used according to the procedures contained in the manual and only for the purpose for which it was designed.
The occupational health and safety directives in force in the Country of destination of the unit must be known and applied in
the place of use.
The manual must be kept in a safe and easily accessible place for staff; it must also be handled with care. It is forbidden to
remove, rewrite or modify the contents of this manual in any way.
The drawings and any other documents delivered with the unit may not be divulged to third parties in that Getidy M.I.Co.,ltd.
is the sole owner and reserves all rights to them.
The partial or total photocopying of the text and illustrations is strictly forbidden.
Getidy M.I.Co.,ltd. reserves the right to make modifications or improvements to the manual or equipment without notice and
without being obliged to update previous production and manuals. The information contained in this manual refers to the unit
the characteristics of which are specified in chap. 5.3.1. "Rating plate".
If the unit is resold, it must be delivered to the new owner together with this manual. In this case, the maker must be informed
of the new owner (see chap. 11.2 "Resale").
2.4 READING THE MANUAL: SYMBOLS AND CONVENTIONS

In this manual, symbols are placed beside certain descriptions, notes, etc.. These symbols are used to attract the attention
of readers to a particular note or explanation. Their meaning is explained below:
SYMBOL DESCRIPTION
STRICTLY FORBIDDEN
This symbol means it is strictly forbidden to perform the operation in question.
Non-observance may cause serious harm to the operator or damage to the equipment.
i INFORMATION AND PRECAUTIONS

This symbol refers to general indications and advice.
Page 6 of 62
IMPORTANT SAFETY INFORMATION
This symbol is used to draw the attention of the reader to particularly
important notions for operator safety.
The manual is divided into chapters and sub-chapters; the figures are numbered with the chapter to which they refer, with the
addition of a progressive number. Eg.: Fig. 3.4-1 (figure n°1 relative to chap. 3.4).
2.5 HOW TO OBTAIN A NEW COPY OF THE MANUAL

If the manual is lost or destroyed, ask Getidy M.I.Co.,ltd. for a new copy.
Provide the following information:
- name and model of the unit;
- name and address where the manual should be sent.
Send your request to the following address:
Zhejiang Getidy Medical Instrument Co.,ltd

Address:N O. 9 Weisan West Road,Hardware Machine Industrial Area,
Tongqin,Wuyi,Zhejiang,China.
Tel:0086-(0)579-87707499 Fax:0086-(0)579-87707467
E-mail:Getidy@Getidy.com
3.Safety
3.1 GENERAL SAFETY WARNINGS
Before using the equipment, read the safety information carefully. Non-observance could cause accidents
or damage to the machine.
--Before using the unit, operators must have perfectly understood the meanings and functions of all the controls.
--Operators must be aware of and know how to apply the safety regulations governing the use of the unit.
Page 7 of 62
--Operators must know and correctly interpret all the indications contained in this manual and those applied to the unit.
--Operators must not perform operations on their own initiative or operations that are not part of their job.
--The responsible authority is responsible for the professional training of operators.
--In the event of malfunctions or potentially dangerous situations, operators MUST immediately report the situation to the responsible
authority.
--It is strictly forbidden to use or neutralize the safety devices.
--Make sure the unit is powered at the correct voltage.
--Make sure the unit is earthed and conforms to the standards applicable in the country of installation.
--Never dismantle the unit.
-- Do not remove the outer safety guard. Even if the unit is not in operation, its cooling fan is always on if power supply to the
machine is connected. Danger of injury to hands (see chap. 3.4 "Residue risks").
--The high voltages inside the unit are dangerous.
--If it is not possible to disconnect the power supply, disconnect the mains supply.If this is distant or not visible by the person carrying
out the maintenance work, place the sign, "Work in progress" on the mains switch after it has been turned "OFF".
--Keep the area around the unit clean and dry.
--Do not use solvents on the label.
--Do not remove the label on the unit. If necessary, ask for a new one.
--Clean the unit with a damp cloth after checking that the power lead is not connected (before using the unit again, remove any traces
of moisture).
--Do not pour water onto the unit or any other liquids that could cause short circuits or corrosion.
--Do not touch the unit with wet hands or if it is wet; always follow the precautions required for the use of electrical equipment.
--The unit was not designed for use in the presence of gas or explosive vapours.
--Do not submit the unit to excessive mechanical stress such as impacts or strong vibrations.
--Do not lean over or stand in front of the door when opening it as there is a risk of scalding from escaping steam (see chap. 3.4.
"Residue risks").
--The used water in the discharge tank may, if not properly sterilized, contain contaminated residues: wear latex safety gloves
while draining (see chap. 6.6 "Tanks: instructions for filling and emptying" and chap. 3.4. "Residue risks").
--Before transporting the machine, drain both water tanks. Use the supplied drain tube and follow the instructions for draining
(see chap. 6.6 "Tanks: filling and emptying" ).
3.2 INTENDED USE

JQ-A series Steam sterilizer: a unit designed and developed for the sterilization of instruments, present in
medical, dental, veterinary or podology surgeries, that can be sterilized by steam between 121 °C and 134 °C .
Page 8 of 62
The unit is for professional use only and may only be used by qualified persons. The unit must only be used for the purpose it
was designed for.
i The manufacturer cannot be held responsible for any breakage, damage or malfunctioning
of the unit if the machine has not been used correctly, been used inappropriately or not
adequately maintained.
3.3 SAFETY DEVICES
Electrical safety
Description Effect
Double-pole thermal safety switch for protecting

Disconnects main electrical power supply.
the device against short-circuits.
Protection of the electronic board against

short-circuits: both the transformer and the Disconnects one or more low-voltage circuits.
entire low- voltage circuit are self-protected.
Page 9 of 62
Thermal protection
Description Effect
The electronic board, the vacuum pump and the vibration
Temporary cut-off to permit cooling.
pump are all protected by a thermostat.
Thermal protection of the unit: the device is blocked if Alarm message and use of the machine is prevented due to
made to work under conditions that do not fall within unsuitable environmental parameters.
the ambient temperature range.
Resettable safety thermostat, complying with PED
97/23/CE standards, for protecting the steam generator Disconnection of power supply to the steam generator.
from over-heating
Resettable safety thermostat, for protecting the heating Disconnection of power supply to the resistances.
resistance of the chamber
Safety valve, complying with the PED 97/23/CE standards, Discharge of steam and re-balancing of pressure to
for protecting the unit from over-pressure. safety values.
Mechanical safety devices
Description Effect
Door safety micro-switch: ensures that the door closes Message indicating wrong door position.
correctly.
Door lock micro-switch: shows the correct position of the

Indication that the door is not locked.
locking system.
Page 10 of 62
Door lock: electro-mechanical device that prevents the Prevents the door from being opened while the unit is in
door from being opened accidentally. operation.
Extractor tool. Used to avoid Prevents burns while removing the trays containing the
touching the inner parts sterilized instruments.
of the unit.
Control devices
Description Effect
Pressure levelling: restores the system to its normal Automatic pressure re-balancing inside the
pressure values, in the event of manual stops or alarms sterilization chamber.
and/or arnings during the cycle.
System for evaluating process parameters, In the event of faults during the cycle, the program in progress
managed entirely by the microprocessor. is stopped immediately and alarms are generated.
Constant monitoring of the device: the components of the Generation of alarm messages and/or warnings in
autoclave are constantly monitored during operation. the event of faults.
It is forbidden to remove, modify, tamper with or in any way neutralize the safety devices.
i Getidy M.I.Co.,ltd. declines all liability for accidents to people or damage or malfunctions
of the unit if the above instruction is not observed.
Page 11 of 62
Periodically check the safety systems (see chap. 10 "Maintenance").
3.4 RESIDUE RISKS

During the normal work cycle, the operator is exposed to certain risks that cannot be completely eliminated due to the nature
of the unit.
-- Danger of burns.
1. When the sterilizer finishes the sterilization cycle and the door is opened to remove the sterilized instruments, the
inner parts of the boiler and door are still very hot. Do not touch these directly in order to avoid getting burnt (Fig. 3.4-1). Use
the relative extractor tool (chap. 3.3 "Safety devices").
2. When opening the door, do not stand over or in front of it as you may be scalded by the steam (Fig. 3.4-2).
Fig. 3.4-1 Fig. 3.4-2

NO! NO!
-- Danger of contamination.
The water used in the discharge tank may, if not properly sterilized, contain contaminated residues: wear latex safety gloves
when draining (chap. 3.5).
-- Danger of injury to hands . Even if the unit is not in operation, its cooling fan is always on if power supply to the machine
is connected (see chap. 3.5). Do not remove the outer safety guard before disconnecting power supply.
Page 12 of 62
3.5 SAFETY SIGNS ON THE UNIT
ATTENTION: when the pressure of inside chamber over than 2.60Bar,the safe
valve will working to leak the high temperature steam.
ATTENTION: Hot surface.
These signs must not be removed, covered or damaged.
3.6 PERSONAL PROTECTIVE EQUIPMENT (PPE)

Latex safety gloves.
4. Receipt and handling

4.1 WEIGHT AND DIMENSIONS OF PACKAGING
Overall dimensions of packaging

A=575mm
B=555mm
C=665mm
A
Total weight of packaging
JQ-A-18 JQ-A-23
C
B 62KG 64KG
Fig. 4.1-1
Page 13 of 62
4.2 RECEIPT AND HANDLING
On receipt of the machine, check that the packaging is intact (keep it for future despatches).
Open the packaging and check that:
--the supply corresponds to the technical specifications (chap. 4.3 "Description of contents");
--there is no evident damage.
If any damage or missing parts are discovered, inform the hauler, wholesaler or Getidy M.I.Co.,ltd. immediately, providing all
details.
Handle the packed unit as described in chap. 6.1. "Work environment: positioning" (Fig. 6.1-1).
4.3 DESCRIPTION OF CONTENTS
Description Specifications Quantity

JQ-A Series Steam sterilizer 18 / 23 litre autoclave 1
Trays Trays in Stainless steel 3
Tray carrier Support with 5 compartments in stainless steel 3
Extractor pincer Pincers for extracting trays 1
Water drainage tube Transparent PVC tube with quick fit attachment 1
Power lead Cable with VDE socket - L = 1.5 m 1
Instructions manual This manual 1
Fuse 10A 2
Sealing of door 1
Getidy CD software of open sterilizer record. 1
4.3.1 Optional devices
Page 14 of 62
Description Specifications Quantity
Mini-printer Printing device external to the unit 1
External memory U Disk(1GB) 1

5.Description of unit
5.1 DESCRIPTION OF UNIT
i JQ-A series Autoclave:

totally automatic steam sterilizer for sterilizing instruments both loose and packed in bags.
5.1.1 Front elements
1.Control panel.
Used to set, visualize and control all the functions of the
unit and to print useful information. The functions of the 2
various buttons are explained in chap. 5.1.4 "Description
of control panel" and chap. 6.5 "How to use the control
panel".
2. Handle for opening the door.

The safety lock is located inside.
3
3. Port for "U Disk" . 4
4. ON-OFF button. 6
1
5. Connector for draining used-water. 5
6. Connector for draining clean-water. Fig. 5.1.1-1

Page 15 of 62
9
Devices on the front of the unit with the door open 8

7. Door cover.
8 . Sealing of door..
9. Air filter.
10. Closing mechanism with electromagnetic pin and
internal safety micro-switch.
7
10
Fig. 5.1.1-2
5.1.2 Rear elements

1. Feeder socket(power filter).
2. Fuse fitting.
3. Connection for min-printer. 6
4. Connector for deflation.
5. Safety valve.
6. Radiator. 5
2
Fig. 5.1.2-1
1 3 4
Page 16 of 62
5.1.3 Upper elements
1. Manual filling inlet for distilled water.
2. Tank, situated inside the unit, under the 1
object-storage compartment. 2
Fig. 5.1.3-1
5.1.4 Description of control panel
1.LCD graphic display (240x160 dots).
Includes a control bar, always present, that refers directly to
the 3-button pushbutton panel situated beneath it.
2. Select button.
3. UP button. 1
2
4. DOWN button.
3
5. START or STOP button. 4
To use the control panel correctly, read chap. 6.5 "How to use
the control panel".
5
Fig. 5.1.4-1
Page 17 of 62
5.2 OVERALL SPACE REQUIRED
200
660
R
34
0
460
450
115 410 50 40 260
575 300 580 5

460
580 880
Overall dimensions of the machine with door closed

JQ-A-18 JQ-A-23
L =460mm
H =450 mm
D = 580mm
Overall dimensions of the machine with door Opened
JQ-A-18 JQ-A-23
L =660 mm
H =450 mm
D = 880mm
Weight of the machine
JQ-A-18 JQ-A-23
Empty: 48 kg. Maximum weight with full tank and maximum Empty: 50 kg. Maximum weight with full tank and maximum
load: 57 kg. load: 62 kg.
5.3 TECHNICAL DATA AND NOISE
Page 18 of 62
CHARACTERISTICS JQ-A-18 JQ-A-23 CHARACTERISTICS JQ-A-18 JQ-A-23
Power supply voltage 220V 10% Chamber capacity 18 litres 23 litres
Mains frequency 50- 60Hz Usable space of chamber 190x145x285mm 190x145x385 mm
Power output 1500W Operation control Microprocessor Microprocessor
Absorbed current 10A Capacity of clean-water tank 4L 4L
Sterilization cycles 8 sterilization cycles Capacity of Used-water tank 3.5L 3.5L
Vacuum test Dimensions of Diameter:250mm Diameter:250mm
Test cycles Bowie & Dick test Depth:350mm Depth:450mm
sterilization chamber
Helix test
Range of environmental --Indoor use
Weight for support area
conditions in which the unit --Altitude up to 2000 m (full tank and chamber 3.07 kg/ 3.21 kg/
was designed to operate. --Temperature: +5~+40 °C with maximum weight)
--Max. relative humidity 85%
*Note: in this manual, the word "pressure" always refers to "relative pressure".
**Usable space
This is the internal capacity of the sterilization chamber available for material to sterilize (fig. 5.3-1).
Usable space 18 litres=7.85litres Usable space 23 litres=10.60litres
Fig. 5.3-1
285 190 385 190
145
145
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5.3.1 Rating plate
The rating plate (Fig. 5.3.1-1) lists the main data and characteristics of the unit, the information required to identify it when
ordering spare parts and/or when requesting information.
JQ-A-18 23
200812999 2008-12
Fig. 5.3.1-1
The label of the unit contains symbols the meaning of which is shown below.
Symbol Description
"SERIAL NUMBER"
SN The symbol must be accompanied by the manufacturer's serial number.The serial number
must be adjacent to the symbol.
"PRODUCTION DATE
The symbol must be accompanied by the year.
The year must be composed of 4 digits.
"WARNING, READ THE INSTRUCTIONS MANUAL"
Page 20 of 62
5.3.2 Noise level
The unit has been designed and built to reduce noise to less than 50 dB(A).
5.4 EXTERNAL PRINTER

The unit is set in such a way that the data regarding the sterilization cycle in progress is always printed, as well as the type of
cycle selected, the phase of the cycle, the temperature and pressure values, and the split and total work times in minutes.
When each cycle is completed, the printer also produces a summary report of the result of the cycle and the total time taken,
regardless of whether the cycle was successful or not and regardless of whether it was stopped manually or an alarm was
generated. The function of printing the summary report can be excluded if desired (chap. 7.5.3 "printer set").
--The printer only works if paper is inserted.
--If no roll of paper is inserted, the printer does not work.
--The red POW LED is always on while the printer is working.
--The green SEL LED flash indicates a problem, e.g.: the paper has
finished, the cover is incorrectly closed, etc..
--Press the OPEN button open the cover, feeds the paper.
--Press the LF button the paper out automatically,press again stop.
Use rolls of thermal printer paper with the following characteristics:

width: 55 - 56 mm
maximum diameter: 40 mm . External printer
Do not expose thermal printer paper, both before and after use, to direct sunlight, heat or
humidity.
Avoid direct contact with materials in polyvinyl, as well as solvents and various derivatives
(filing envelopes in PVC, acrylics and paper treated with ammonia vapours).
Rolls should be kept in a dry place with humidity of no more than 70% and direct temperature
lower than 35 ° centigrade.
Page 21 of 62
6.Installation and first start-up
6.1 WORK ENVIRONMENT: POSITIONING
The unit is packed as follows: covered with a hood in polyethylene with blisters, protected by totally recyclable mouldings in
foamed polyethylene, and placed inside a corrugated cardboard box, certified for transportation by sea.
Lift the unit with care and do not turn it upside down.
The packaging and the equipment are fragile, handle with care. Transport as fragile. THE HANDLES
ON THE PACKAGING (1 of Fig. 6.1-1) MUST ONLY BE USED FOR VERTICAL LIFTING. Keep in a dry and
protected place. The packaging must be kept for the whole guarantee period.
i NOTE : keep the original packaging and use it to transport the unit.The use of different packaging may damage
the product during transport.
The unit must be removed from its packaging using the straps provided for the purpose: this operation must be carried out by
two people at the same time (Fig. 6.1-2):
--Remove the upper protecting piece(s);
--Two people must then lift the unit out, keeping it in a horizontal position all the time;
--Place the unit on the work surface and then remove the straps by lifting it up slightly.
1
ATTENTION: follow the indications
shown in figure 6.1-2.
--The unit should be installed inside a laboratory,

which is accessible only to authorised personnel.
Fig. 6.1-1
--Position the unit on a flat and horizontal surface (Fig. 6.1-3). Fig. 6.1-2
Page 22 of 62
--It is recommended to assemble the distance - screws ( supplied) as described in the pictures ( a , b ) in order to assure the
correct distance between the back wall (Fig. 6.1-3).
--Do not place the unit near sources of steam or where it could be splashed by water, which could damage the internal electronic
circuitry.
--Do not install the unit where there is poor air circulation (Fig. 6.1-4).
--Do not place the unit near sources of heat (Fig. 6.1-4).
--The area where the unit is placed must be lit in accordance with standard UNI 12464-1.
--Acceptable environmental conditions:
temperature from 5 to 40 °C --- max.humidity 85% without condensation ---- max.altitude 2000 m.
Fig. 6.1-3 Fig. 6.1-4
10cm
6.2 INSTALLING THE UNIT

Installation is a fundamental operation for the subsequent use and correct functioning of the unit.
ATTENTION: the unit MUST be installed by specialised technicians.

After installing the unit, always fill out the installation sheet and update the service booklet,
completing the space for installation with the respective date and signature.
This unit has been designed for use in a normal environment (see chap. 5.3 "Technical data"); it is necessary, however, to
follow the instructions given below.
-- Install the unit so that the power lead does not kink or become squashed but has a free run to the socket.
Page 23 of 62
--The unit must be placed so that the plug is accessible.
--Place the unit at a height that will allow the user to inspect the entire sterilization chamber and clean it with ease.
--Do not place trays, newspapers, containers of liquids, etc. on the unit: the ventilation grilles must not be blocked.
--Do not lean on the door when it is open.
--When emptying the discharge tank directly into the waste pipes, position the unit at a height above the drain.
ATTENTION: Once installed and connected to an electrical power point,

the unit is ready to use.
6.3 ELECTRICAL CONNECTIONS
ATTENTION: Electrical connections must be made by specialised technicians.
--Check that the power supply voltage indicated on the rear label (Fig. 5.3.1-1) corresponds to that available at the point of
installation.
--The unit must be connected with an overload cut-out switch to a system fitted with an adequate earth system that conforms
to the standards applicable in the country of installation.
--The system must be connected according to current standards.
--Max. variation in mains voltage: +/- 10%.
-- A differential switch featuring the following characteristics must be installed upstream of the power socket of the unit:
differential sensitivity: 0.03 A; nominal current: 10 A.
--Connect the supplied cable to the rear of the unit.
--Position the unit so that the plug is accessible.
Do not allow the lead to bend tightly and do not place any object on it.
Do not use extension leads.
Only use the original lead.

ONLY USE ORIGINAL SPARE PARTS.
If the unit does not function correctly, please refer to Appendix 9 "Troubleshooting" of this manual for possible causes. For
further information or repairs, please contact your supplier or the technical department of Getidy M.I.Co.,ltd.
Page 24 of 62
WARNING: The unit conforms to the electrical safety requirements of the Standards Institute and comes supplied
with a double-pole plug that ensures the unit is earthed.
A fundamental safety requirements is to check that the electrical system is adequately earthed and that the capacity
of the system and the sockets are suitable for the power of the unit indicated on the label (see chap. 5.3.1 "Rating
plate"). Have the system checked by qualified personnel.
Getidy M.I.Co.,ltd. DECLINES ALL LIABILITY IF THE ABOVE IS NOT OBSERVED.
6.4 FIRST START-UP

The unit is packed with the door closed.
--Take out the equipment from the sterilization chamber and remove the packaging.
--Connect the unit to the power socket following the safety instructions described in chap. 6.3 "Electrical connections".
--Switch on the unit using the ON-OFF switch (4 of Fig. 5.1.1-1).
--After the welcome message, the message "Please add Distill water " appears, that disappears after a few seconds.For
filling, read the instructions in chap. 6.6 "Tanks: instructions for filling and emptying".
1
6.5 HOW TO USE THE CONTROL PANEL
The JQ-A series steam sterilizer is complete with an LCD graphic 2
user interface (1 of Fig.6.5-1),with the 4-button pushbutton 3
panel situated beneath it (2-3-4-5 Fig.6.5-1).
The four buttons on the pushbutton panel (2-3-4-5 of Fig.6.5-1) 4
are used to perform all the programming,use and maintenance 5
functions of the unit.
Fig.6.5-1
Page 25 of 62
6.6 TANKS: INSTRUCTIONS FOR FILLING AND DRAINING
The unit features two separate tanks : one for the clean water required for the cycles, and one for the used water that is
collected at the end of the cycles. Both tanks are connected with drain valves.
Filling with distilled water for the first time
1.Switch on the unit with the ON-OFF button.The following message will appear on and flash the display.
PROMPT PROMPT
134.0°C
03min
134.0°C
03min
1
1times 1times
2
! Please add distill water. ! Please stop add distill
water.
HELP Press KEY. HELP Press KEY.
USB PRINTER USB PRINTER

10-12-2008 12:56:30 00001 02/50
Fig. 6.6-1 10-12-2008 12:56:30 00001 02/50 Fig. 6.6-2
2.Lift the upper cover (1 of Fig. 6.6-3) and manually pour distilled
water in through the inlet (2 of Fig. 6.6-3), observing the amounts
indicated in chap. 5.3 "Technical data".
Fig. 6.6-3
WARNING: only use good quality clean water
(Appendix 8 "Quality of process water").
3. Once filling is complete, that can also be confirmed by the level indicator (2 of Fig. 6.6-3) situated next to the inlet, the
following screen appears on the display: please add distill water! will disappear.
Subsequently, when the unit is in use, each time the water reaches the MIN level, the message "please add distill water " will
reappear and it will not be possible to perform any work cycles or tests until the tank has been filled.
Page 26 of 62
Adding distill water
1. When clean water tank is full,t he following screen appears on the display: please stop add distill water! (Fig.6.6-2).and
make a sound di three times.
2. Fill the clean water tank with distill water, using the respective inlet (2 of Fig. 6.6-3).
WARNING : always use good quality clean water (Appendix 8 "Quality of process water").
WARNING: before transporting the unit, drain both water tanks .Use the supplied tube.To empty the clean water tank,
fit the end of the tube with the connector into the connector at the bottom of the front panel (5-6 of Fig. 5.1.1-1 ), and
the other end into an empty container.To empty the used water tank, follow the instructions given below.
Emptying used water PROMPT

134.0°C
If the used water tank is full, the following message appears 03min
on and flash the LCD display of the control panel(Fig.6.6-4). 1times
1.To empty the used water tank:
Please discharge waste
! water.
ATTENTION: DANGER OF CONTAMINATION. The used
water in the discharge tank may, if not properly sterilized, HELP Press KEY.
contain contaminated residues; wear latex safety gloves USB PRINTER
when draining (chap. 3.4 "Residual risks"). Fig.6.6-4
10-12-2008 12:56:30 00001 02/50
NEVER REUTILISE USED WATER.

2.Take an empty container,insert the transparent tube supplied with the unit into the connector at the bottom of the front panel
(5 of Fig. 5.1.1-1). At the end of the drainage operation, remove the tube from the connector by pressing on the clip.
WARNING: This operation is fundamental for the correct operation of the unit.
ATTENTION:If the autoclave working,the distill water in clean tank not enough or the used
tank are full,this time the cycle also can keep on until the cycle end,but next time before the
cycle the operator must clear all alarms,befor working.
Page 27 of 62
Maximum load
Never exceed the max. load specified in Appendix 5 "Description of Programs".
--Always observe the maximum load, established and checked by Getidy M.I.Co.,ltd., for each solid material to sterilize.
--The maximum internal load of the unit is shown in Appendix 5.
--The unit is tested and only provides the indicated performance levels if the internal load does not exceed the above values
for the maximum full load.
7. Operation
7.1 Prepare work before operation
Before beginning to operate the unit, carefully read all the warnings indicated in this manual,
especially chap. 3 "Safety".
NEVER LIFT the upper cover that covers the object-storage compartment and the water inlet
during the sterilization cycle.
7.1.1 Trun on.After pressing the switch ON-OFF

then fill with the distiller water as chap 6.6.
7.1.2 set time. According the chap 7.5.1 setup the
information of Year-month-day and hour-minute
-second .According thechap 7.5.2 setup the
user information .
7.1.3 load the material
Before starting the selected cycle,load the

material to sterilize into the unit:
--open the door.(Fig.7.1.3-1) Fig.7.1.3-1
Page 28 of 62
--Place the trays with the material to sterilize inside the unit.
In order to load the material to sterilize correctly,read all the instructions given in Appendix 1 reparing the
instruments for sterilization Appendix 2 Packaging and Appendix 3 Arranging the load .
--Close the door:pull the handle towards you while pushing the door in,and then turn the handle back toward the unit.
--Select the cycle type following the instructions give in chap7.2.
7.2 SELECTING A STERILIZATION CYCLE PROGRAM PROGRAM LIST

Press the button Select on the control panel,the Fig.7.2-1
will been show on the screen, then the light cursor will located at 1. Prompt 134 !"# 03m-1Times
the Program List .press the START and STOP the Fig.7. Program List 2. Solid 134 !"# 04m-1Times
2-2 will been show on screen,select the revelant program according User-Definned 3.Hollow 134 !"# 04m-3Times
the instruments by button Up or Down press the Test Program 4.Sanguinary134 !"# 18m-3Times
button START and STOP to confirme and Exit.this time the System Set
Operation. 121- !" 20m-1Times
5.Solid Operation.
screen also show Fig.7.2-1 but the light cursor located at Exit
press the button,the screen will show Fig.7.2-3.press the button
Record
HELP Press KEY. 6.Hollow 121 !"# 20m-3Times
HELP Press KEY.
START and STOP the machine will working. Information 7.Glass 121 !"# 20m-1Times
Exit 8.Tampon 121 !"# 30m-3Times
PROMPT Fig.7.2-1 Fig.7.2-2

134.0°C i ATTENTION
03min
1times 1.The program Name which be shown on the screen just selected by the user. And
also change according the selection by the user.
! Press ! START " 2. Everytime when the user switch the ON-OFF the program name which show
Operation.
on the autoclave are same as last time.
HELP Press KEY.
USB PRINTER
10-12-2008 12:56:30 00010 10/50 Fig.7.2-3
Page 29 of 62
7.3 SET USED-DEFINNED
Press the button Select on the control panel,the Fig.7.2-1 will been show on the screen,
User-Definned then the light cursor will located at the Program List ,use the button Up or Down
let the light cursor located at the User -Definned ,press the button START and STOP
Temperature 134 !" the screen will show the Fig.7.3-1.use the Select select the four items Temperature
Sterilization drying Time Vacuum Times And each item the relevant parameter
Sterilization 04 min can be increase by the button Up and reduce by the button Down .
Drying Time
Operation.
04 min i Attention:
1.temperature: have two kinds temperature can be selected:134 or 121 .
Vcuum Times
HELP Press 3 times
KEY. 2.Sterilization: the Min time is ---4 minuters.
3.Drying time: the Min one is :4 minuters Max time :60Minuters.
Fig.7.3-1 4.Vacuum times: have two kinds temperature can be selected : 1 times and
3 times.
7.4 TEST PROGRAM
Test Program
B&D Test Press the button Select on the control panel,the Fig.7.2-1 will been show on the screen,
then the light cursor will located at the Program List ,use the button Up or Down
Helix Test let the light cursor located at the Test Program press the button START and STOP
Vacuum Test the screen will show the Fig.7.4-1.Use the button Up or Down select one between
the B&D Test and Helix Test program,press the button START and STOP confirme
Operation.
Cleaning and Exit,then press the button START and STOP and two times the B&D Test or
HELP Press KEY. Helix Test will be operated.
Page 30 of 62
7.4.1 Vacuum Test
Press the button Select on the control panel,the Fig.7.2-1 will been show on the screen, then the light cursor will located
at the Program List ,use the button UP or DOWN let the light cursor located at the Test Program press the
button START and STOP the screen will show the Fig.7.4-1.Use the button UP or DOWN select the
Vacuum Test,press the button START and STOP the Fig 7.4.1-1 will show on screen.press the button UP ( just
mean YES ) the Fig.7.4.1-2 will show on screen.
The Fig.7.4.1-2 means the bigining of the first step of vacuum test.Vacuum time: 5 minuters.
After 5 minuters later the Fig.7.4.1-3 will show on the screen.the machine will record the pressure P1 .The Fig.7.4.1-3
means the bigining of the second step of vacuum test.this step will keep 5 minuters.
5 times later, the Fig.7.4.1-4 will show on the screen,the machine will record the pressure P2 ,the Fig.7.4.1-4 means the
beginning of the third step of vacuum test.This step will keep 10 minuters.
10 minuters later,the Fig.7.4.1-5 will show on the screen,the machine will record the pressure P3 ,the Fig.7.4.1-5 means
the whole vacuum test are finished,the autoclave value system will judge the vacuum test is ok or not. If ok the Fig.7.4.1-6 will
show on the screen,if not pass the Fig.7.4.1-7 will show on the screen.
Vacuum Test Vacuum Test Vacuum Test Vacuum Test Vacuum Test
YES NO Vcauum-Operation Record Record Record
05:00 05:00 10:00 00:00

-0.000bar -0.890bar -0.890bar -0.890bar
P1 -0.890bar P1 -0.890bar P1 -0.890bar
P2 -0.888bar P2 -0.888bar
P3 -0.885bar
Fig.7.4.1-1 Fig.7.4.1-2 Fig.7.4.1-3 Fig.7.4.1-4 Fig.7.4.1-5 Fig.7.4.1-6
Vacuum Test
ATTENTION: the VACUUM TEST can only be activated
with the machine cold, i.e. WITHIN 3 MINUTES FROM
SWITCHING ON THE UNIT.
Fig.7.4.1-7
Page 31 of 62
7.4.2 Cleaning
Press the button Select on the control panel,the Fig.7.2-1 will been
show on the screen, then the light cursor will located at the Program List YES NO Cleaning-Program
use the button UP or DOWN let the light cursor located at the
Test Program press the button START and STOP the screen 04:00
will show the Fig.7.4-1.Use the button UP or DOWN select Last Time
the Cleaning,press the button START and STOP the Fig 7.4.2-1 00-00-2000
will show on screen. 00:00:00
(1)Press the button UP ( just mean YES ) the Fig.7.4.2-2 will show
on screen.working time: 4 min.
(2)Press the button Down ( just mean NO ) means cancel and
exit. Fig.7.4.2-1 Fig.7.4.2-2
(3) Last Time....... means last time when you use this program.
System Set
7.5 System Set Time Set
Press the button Select on the control panel,the Fig.7.2-1 will been show on the screen,use User input
the button Up or Down let the light cursor located at the system Set press the button Printer set
Operation.
START and STOP ,the Fig.7.5-1 will show on the screen.use the button Up or Down
Exit
Select and setup the three items: Time set User input Printer Set .
Fig.7.5-1
7.5.1 Time Set Time Set

When the screen show the Fig.7.5-1,Select the item Time Set and press the button START and
STOP the screen will show the Fig.7.5.1-1.use the button Select to Select the Element : D-M-Y H-M-S
D(day)-M(month)-Y(year)-H(hour)-M(minuter)-S(second) . Use the button Up or Down 10 12 08 12 56 30
to adjust the Number. After setup press the button START and STOP confirme and exit.
Fig.7.5.1-1
Page 32 of 62
7.5.2 User input
Password Password Password
When the screen show the Fig.5-1,Select the item
User input press the button START and STOP OK OK
the screen will show the Fig.7.5.2-1. Press ABCDEFGHIJKLM ABCDEFGHIJKLM ABCDEFGHIJKLM
the button Down the light scroll will locate on NOPQRSTUVWXYZ- NOPQRSTUVWXYZ- NOPQRSTUVWXYZ-
A .Press the button Select six times,means 0123456789 0123456789 0123456789
the password is six A . Then the screen will show Now,input name Now,input name
as Fig.7.5.2-2.Use the button Up or Down XXXXXXXXXXXXXXXX XXXXXXXXXXXXXXXX
move the light scroll from A to 9.press the button save Cancel
Select Select the each item in turn until it's end,
then press the button START and STOP the Fig.7.5.2-1 Fig.7.5.2-2 Fig.7.5.2-3
Fig.7.5.2-3 will show on screen. Press the button Up
the system will save the information,press the button Down the system will cancel the information which been input.
ATTENTION The letter which made up of theclinic name not over than 16.
i ATTENTION Chap7.7 Information (Fig.7.7-1).In this item,if the Use name not be set up befor,
here the use name will be empty.The printer paper of sterilizer record also the same.
7.5.3 Printer set
when the screen show the Fig.7.5-1,Select the item Printer set press START and
STOP the Fig.7.5.3-1 will show on the screen.press the button Up Select
the ON or OFF .
Printer Set
(1)ON means the external printer and the autoclave connection been Opened. 1. OFF
(2) OFF means the external printer and the autoclave connection been Closed.
After Select the ON or OFF,then press START and STOP confirme and exit.
Fig.7.5.3-1
Page 33 of 62
7.6 Record No=01
when press the button Select the Fig.7.2-1 will show on the screen.
Use the Up or Down let the light cursor located on the item GETIDY MEDICAL Download?
Record press START and STOP ,the Fig.7.6-1 will show on the Ver. 2.0 All Prt USB
screen.Press the UP or Down check each record (No=1 .No=50) User name
...............
if the screen show the Record No=1,you want to download this record,press the
button START/STOP ,the Fig.7.6-2 will show on the screen.
NO
1. All means download the all records before, this operation just press the
button Select .download it.
2. Prt means just print the near sterilizer record use the external printer.
Press the Up print it. Fig.7.6-1 Fig.7.6-2
3. USB means download the near sterilizer record into the USB.press the Down download it.
4. No means don t print the record or don t download the record to USB.press the button START and STOP is ok.
Attention:
(1)the autoclave can stock memory Maxium 50 times,if over than 50 times And not be download,the No=1
i will be delete automatically,and the NO=2 will Turn into NO=1.No=3 will Turn into No=2 by tune.
(2)Pls check the information of record quantity which have been stocked in autoclave at the light corner
of screen.For example : 10/50 means the autoclave have 10 pcs memory stocked. (Fig.7.2-3).
7.7 Information
when press the button Select the Fig.7.2-1 will show on the screen. Use the Up Information
or Down let the light cursor located on the item Information press START and
STOP ,the Fig.7.7-1 will show on the screen. Total number
00001
(1) Total number means the Total use times after the autoclave been installed.
(2) User name The name of clinic,if the uer not setup this one,the screen will no User name
information been showed. ???????????????????
(3) Serial number the Serial numbe of this autoclave. Serial number
2008 12 10 999
Fig.7.7-1
Page 34 of 62
7.8 Three pre-vacuum sterilization process graphic
Example: Sanguinary 134 -18min-3times
Fig.7.8-1 Fig.7.8-2 Fig.7.8-3 Fig.7.8-4 Fig.7.8-5
Sanguinary Sanguinary Sanguinary Sanguinary Sanguinary
18min-3times 18min-3times 18min-3times 18min-3times 18min-3times
134°C-2.1bar 134°C-2.1bar 134°C-2.1bar 134°C-2.1bar 134°C-2.1bar
09:55 04:00
00:07 03:15 09:53 10:53 15:02
59.1 65.5 131.5 102.5 106.5
-0.178bar -0.800bar 1.856bar -0.020bar -0.730bar
57.4 65.4 131.4 102.4 105.4
1 TIMES VACUUM 1 TIMES PRESSURE 2 TIMES VACUUM 2 TIMES VACUUM 2 TIMES PRESSURE
STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT
The first time The first time Exhaust steam The second times The second times
beginingof beginingof until 0.000bar. beginingof beginingof
pre-vacuum. rise pressure. pre-vacuum. rise pressure.

Sanguinary Sanguinary Sanguinary Sanguinary Sanguinary
04:00 18:00
19:52 20:52 24:57 30:23 48:18
131.5 115.5 103.1 135.2 135.5
1.856bar -0.020bar -0.710bar 2.120bar 2.133bar
131.4 109.4 103.0 135.1 135.4
3 TIMES VACUUM 3 TIMES VACUUM 3 TIMES PRESSURE STERILIZING EXHAUSTING
Exhaust steam The third times The third times beginingof After sterilization,
until 0.000bar. beginingof beginingof sterilization. start to exhaust
pre-vacuum. rise pressure. until 0.000bar.
Page 35 of 62
Sanguinary Sanguinary Sanguinary Sanguinary
18min-3times
134°C-2.1bar
18min-3times
134°C-2.1bar
18min-3times
134°C-2.1bar
18min-3times
134°C-2.1bar
END
10-12-2008
18:00 02:59 00:59 14:02:45
49:18 64:21 66:21 67:20 067min
115.2 81.5 77.9 65.2
00002 times
-0.002bar -0.889bar -0.003bar -0.002bar
103.0 78.5 76.7 65.0
DRYING DRYING DRYING USB PRINTER
STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT
Beginningof Temporality vacuum Vacuum pump stop, Readin to U disk or The sterilization
drying,vcauum value is maximal. start to balance with external printer, cycle is over,operator
pump operate. atmosphere. Wait for 30 second. can open door.
7.9 One pre-vacuum sterilization process graphic
Example: Prompt 134 -03min-1times
PROMPT PROMPT PROMPT PROMPT PROMPT
09:39 03:00
00:21 02:40 08:58 09:58 14:20
33.5 47.5 131.5 101.5 135.5
-0.281bar - 0.800bar 1.830bar 0.005bar 2.160bar
33.4 47.4 131.4 101.4 135.4
1 TIMES VACUUM 1 TIMES PRESSURE 1 TIMES PRESSURE 1 TIMES PRESSURE STERILIZING
The first time The first time Exhaust steam The second times Beginningof
b eginningof beginningof until 0.000bar. beginning of sterilization.
pre-vcauum. rise pressure. rise pressure.
.
Page 36 of 62
Fig.7.9-6 Fig.7.9-7 Fig.7.9-8 Fig.7.9-9
PROMPT PROMPT PROMPT
03min-1times
134°C-2.1bar
03min-1times
134°C-2.1bar
03min-1times
134°C-2.1bar
END
10-12-2008
09:00 13:37:15
17:20 18:20 27:20 027min
135.4
00002 times
2.150bar 115.5 66.5
135.3
0.005bar 0.005bar
107.4 66.4
EXHAUSTING DRYING USB PRINTER
STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT STOP:PRESS 3 S EXIT
After sterilization, Beginning of Readin to U disk or The sterilization

start to exhaust drying,vacuum external printer, cycle is over,operator
until 0.000bar. pump operate. Wait for 30 second. can open door.
7.10 Abnormal Exiting

If the User want to stop the working when the device are working,
Abnormal Exiting!
press the button START and STOP three seconds.the device
will stop Abnormally. The Fig.7.10-1 will show on the screen.the 00
Vacuum-Operation
Solenoid Valve which connect the air will open automatically for <134>
balance the pressure in and outside of the chamber. 04:00
00:24 -0.000bar
When the Fig.7.10-1 show on the screen,press the button START
and STOP again,the Fig.7.10-1 will became to Fig.7.10-2. 42.3
-0.286bar
41.5
The vacuum pump will working 4 mins to absorb the water steam 0902-3403-94110516
Wait for....
inside the chamber. 0000-0004-28000000
0812-1300-00000013
Fig.7.10-1 Fig.7.10-2
ATTENTION:When the screen show the Fig.7.10-2,
please do not press the button START and STOP again and wait 4 mins,let the vacuum pump absorb
the water steam inside the chamber.If the operator press the START and STOP before the vacuum
pump stop,the water steam will hurt people when open the door!
Page 37 of 62
7.11 Some indications on screen
Fig.7.11-1 Fig.7.11-2
PROMPT When the door opened,press the PROMPT When the screen show open the door
134.0°C
button START and STOP 134.0°C
before working ,the operator press the
03min
1times
the screen willshow this graphic. 03min
1times
button START and STOP ,will
please open the door.
! Please close the door. ! Please open the door.

10-12-2008 12:56:30 00001 02/50 10-12-2008 12:56:30 00001 02/50
Fig.7.11-3 Fig.7.11-4
PROMPT This indication meams press the PROMPT If the operator want start thecycle,you
134.0°C
button START and STOP 134.0°C
must open the door before working.
03min
1times
then working. 03min
1times
! Open the door before ! Press ! START "

working. Operation.
10-12-2008 12:56:30 00001 02/50 10-12-2008 12:56:30 00001 02/50
ATTENTION:If the autoclave are not working over than 40 seconds and no button be
pressed,the screen will be dark.Touch any button the screen will light again,this kind
of function for protecting the LCD screen and save electricity.
Page 38 of 62
WARNING: when the autoclave is turned off,be sure that the door is either open(a)or completely closed (b).
It is important to avoid the situation shown in c, which is closing the door with handle not completely hooked.
a b c
ATTENTION:DANGER OF BURNS. When the unit finishes the sterilization cycle and the door is opened to remove
the sterilized instruments, the inner parts of the boiler and door are still very hot.These must not be touched directly
in order to avoid getting burnt (chap.3.4 "Residual risks").Use the relative extractor tool.
ATTENTION: DANGER OF BURNS. Do not lean over or stand in front of the door when opening it as there is a risk
of scalding from escaping steam (chap. 3.4 "Residual risks").Use the relative extractor tool.
If the sterilization cycle has not been successful,an error message will be displayed indicating the cause of the problem
(Appendix 9 "Troubleshooting").
ATTENTION : A safety pin automatically locks the door when the cycle starts.The pin only returns to its seat
at the end of the cycle. Attempting to open the door with the door safety device applied may seriously damage
the closing system.Always wait for the end of cycle signal on the LCD display before opening the door.
In the event of an alarm, the door can only be opened after having given consent by means of the respective
button (see 7.6).
Page 39 of 62
8.Maintenance
8.1 SAFETY WARNINGS
Before performing any maintenance operations,carefully read the following safety instructions and,
especially, chap. 3 "safety".
WARNING: when replacing components that directly or indirectly affect safety ,it is essential to only use
ORIGINAL SPARE PARTS.
DANGER: HIGH INTERNAL VOLTAGE.

WARNING:DISCONNECT THE POWER SUPPLY BEFORE STARTING WORK. Non-observance may cause
serious injury to people and seriously damage the unit.
ALL MAINTENANCE OPERATIONS MAY ONLY BE PERFORMED BY THE RESPONSIBLE AUTHORITY OR BY THE
TECHNICIANS AUTHORISED BY THE ASSISTANCE SERVICE OF GETIDY M.I.Co.,ltd.
--Observe the intervals prescribed or shown in this manual.Activates memorandum messages to assist the user in performing
both the ordinary and the extraordinary maintenance operations.
-- It is forbidden to eliminate the safety devices installed on the machine (see chap. 3.3 "Safety devices").
-- Check them at regular intervals.
-- If an effective danger situation arises, press the ON-OFF button (4 of Fig. 5.1.1-1) immediately.
-- Unauthorised people must stay at a safe distance from the machine during maintenance operations.
After maintenance and before starting the unit, the responsible authority must make sure that work has been done
correctly, that the safety devices are active and that no-one is already working the unit.
8 .2 ROUTINE MAINTENANCE
Just like all electric units, this unit must be correctly used,serviced and checked at regular intervals.These precautions will
ensure the unit works continuously, safely and effectively.
To prevent operator hazards, the unit must be subject to regular checks and servicing by the technical assistance service.
--To maintain the unit in good working order, periodically clean all the external parts using a soft damp cloth and normal,neutral
detergent (do not use corrosive or abrasive products).
--Do not use abrasive cloths, pads or metal brushes (or anything abrasive) to clean the metal.
Page 40 of 62
--Before starting each cycle, clean the door seals carefully using a damp cloth.
--The formation of white stains on the base of the chamber shows that the demineralised water used is of poor quality.
Maintenance programme
FREQUENCY OPERATION
Cleaning of the door seal.
DAII.Y General cleaning of the external surfaces.
General cleaning of the internal surfaces.
WEEKLY Cleaning of the sterilization chamber.
Cleaning of the trays and the support.
ANNUALY Maintenance of the safety valve.
EVERY 500 CYCLES Replacement of the bacteriological filter.
EVERY 500 CYCLESReplacement of the seals.
AFTER 10 YEARS Request a structural check of the chamber.
WHEN NECESSARYA Djustment of the closing mechanism.
Cleaning the sterilization chamber, accessories, door and seal.

WARNING: DISCONNECT THE POWER SUPPLY BEFORE STARTING WORK. Non-observance may cause
serious injury to people and may seriously damage the unit.
Sterilization chamber
Clean the sterilization chamber thoroughly (Fig.8.2-1),after having removed the tray support,using a non-abrasive damp cloth.
To dampen the cloth, use only and exclusively distilled or demineralised water. Follow the same procedure for cleaning the
trays and their support. Cleaning the sterilization chamber is important for eliminating deposits that could compromise the
good working order of the machine.To dismount the tray support:
remove the support from the chamber (Fig. 8.2-2), taking care not to damage the probe at the bottom of the chamber. After
Page 41 of 62
cleaning, perform the above operation in reverse order.
Fig.8.2-1
Fig.8.2-2
Do NOT use disinfecting substances to clean the chamber.
Seal and door Fig.8.2-3
Clean the seal and door with a damp cloth(Fig.8.2-3),dampened with

water or vinegar to eliminate traces of lime-scale.Cleaning should be
carried out to remove any impurities that could cause a lack of pressure
in the sterilization chamber and possible cuts in the seal.
WARNING: do not allow residues of lime-scale or dirt to

accumulate on the seal, since these can damage orbreak
it over time.
Page 42 of 62
To maintain the unit in good working order,periodically clean all the external parts using a soft cloth and normal neutral
detergents or just water (do not use abrasive products).
Do NOT wash the unit with direct sprays or high-pressure jets or water ,since any infiltration into the electrical
components could prejudice the working of the machine and the safety systems.
Emptying and cleaning the tanks
WARNING: DISCONNECT POWER SUPPLY. Non-observance may cause serious injury topeople or may
seriously damage the unit.
WARNING: if the unit is not used for more than three days, both tanks should be emptied to prevent deposits
from forming.
1. Empty the clean water tank: fit the end of the tube with the connector into the connector at the bottom of the front of the unit
(6 of Fig. 5.1.1-1) and the other end into an empty container.
2. Empty the internal tank for collecting used water: fit the end of the transparent tube into the connector at the bottom of the
front of the unit (5 of Fig. 5.1.1-1) and the other end into an empty container.
3. At the end of the draining operation, remove the tube from the connector by pressing on the clip.
4. Remove the cover in order to access the tanks:
--unscrew the 6 screws (Fig. 8.2-4); --lift the cover by 45 ° (Fig. 8.2-5) and pull it towards you (Fig. 8.2-6).
Fig. 8.2-4 Fig. 8.2-5 Fig. 8.2-6
Page 43 of 62
5.Carefully clean the tanks with the sponge supplied and water,using it on the spongy side and not on the abrasive side.Clean
with care, paying particular attention to any dirt that may have deposited in the corners.
6. Rinse thoroughly and empty the water used for this operation.
7.Run a sterilization cycle without loading the unit.
WARNING : while performing all cleaning operations, be careful not to damage the floating sensors situated
in the tanks.
8.2.1 Periodic maintenance
WARNING: DISCONNECT POWER SUPPLY BEFORE STARTING WORK. Non-observance may cause serious
injury to people or may seriously damage the unit.
Servicing the safety valve

WARNING: HIGH TEMPERATURE. Only perform this operation when the machine is cold.
1.Access the safety valve mounted at the rear of the machine.
2.Turn the plug located on the upper part of the valve anti-clockwise until it reaches the end of the thread and turns loose.
3.Return the plug to its original position,screw it back on and repeat the operation from the beginning at least a couple of times.
WARNING: this operation ensures the safety valve works correctly over time. Make sure the plug is properly
closed afterwards.
Adjusting the closing mechanism
The closing mechanism of the unit occasionally requires adjusting due to normal settling of mechanical parts and wear on the
seal gasket.This is particularly important as a poor seal may prevent the pressure from increasing to the level set for the
selected program and therefore jeopardise the result of the cycle.Proceed as follows
1. Open the door. Always work with the unit cold.
Page 44 of 62
2.Fit the extraction and adjustment lever between the door gasket and the guard,holding it with its widest part.Slip the tip into
the nut in the middle of the door gasket.
3.Turn the adjustment pin anticlockwise, looking at the door gasket, by 1/8 of a turn (to close).
4.Check that the door closes properly. If the handle is too hard to close, turn a little in the opposite direction (clockwise).
5.Carry out a test cycle to check it is correctly adjusted.
Resetting the safety thermostat

WARNING: the safety thermostat can only be reset by the responsible authority.
To reset the safety thermostat, proceed as follows:
1. Wait for about 10 minutes for the machine to cool down.
2. Unscrew the black protruding cap (the bottom right at the rear of the machine) .
3. Press the red button inside the hole with a pointed object (such as a screwdriver).
4. Screw the black cap on. The machine has now been reset.
After resetting the safety thermostat, reconnect power supply, restart the cycle and make sure the fault has been eliminated.
WARNING: if the fault persists, switch off the unit and call the Technical Assistance Service. Do not reset the
thermostat again. PERFORM THIS OPERATION JUST ONCE.
8.3 EXTRAORDINARY MAINTENANCE

Any jobs not mentioned above are considered as extraordinary maintenance. In these cases, contact specialists authorised
by Getidy M,I.Co.,ltd.
i The Air filter and the gasket are components that are not covered by the guarantee.
Service maintenance
After 1000 cycles or after two years from installation,This can only be performed by specialists authorised by Getidy M,I.Co.,ltd.
Page 45 of 62
WARNING:extraordinary maintenance must only be performed by specialists authorised
by Getidy M,I.Co.,ltd.
Replacing the Air filter
-- Unscrew the Air filter (9 of Fig. 5.1.1-2) by turning it anticlockwise;

--Screw on the new filter by turning it clockwise until it is tight.
Replancing the door sealing
-- Grip the lip of the sealing with two fingers and remove it;
--Clean the seat of the seal with a cloth soaked in alcohol;
--Fit the new seal into the seat located in the door and distribute it evenly around the circumference by applying the same
pressure on the entire gasket with your fingers.Then lift up the lip of the gasket tomake s ure no points have been badly fitted;
--Switch on the autoclave,close the door making sure the correct closing force is required; if necessary,adjust the closing force
with the relative adjustment wrench.
Cleaning the draining water filter
If necessary, cleaning the the draining water filter.Unscrew

the filter as showed in the picture and clean it with water.
Take care that the screw or other object fall down into the
Solenoid valve.( Fig.8.3-1 )
Power fuse
The fuse on the internal card is of the type: 5x20 ,10A.
Fig.8.3-1
Page 46 of 62
8.3.1 Rusting
The unit is made from materials that make it impossible for rust to form on the instruments to sterilize.
The formation of rust on the surfaces of the unit or instruments is caused by the introduction of rusty instruments,even if
made from stainless steel, or of instruments in normal steel that cause galvanisation to take place.
The introduction of a single instrument with a rust stain is often sufficient to form and develop rust on the instruments and in
the unit itself.
WARNING: DISCONNECT POWER SUPPLY BEFORE STARTING WORK.Non-observance may cause serious
If rust forms in the unit,clean the walls of the sterilization chamber and the tray holder using special products for stainless steel,
as described previously in the paragraph "Cleaning the sterilization chamber, accessories,door and gasket".
WARNING: do not use metal sponges or brushes.Use a damp soft cloth to remove dirt stains.
9. Scrapping
9.1 SCRAPPING INSTRUCTIONS
The JQ-A series unit has been manufactured using ferrous materials, electrical components and plastics. To scrap the unit,
separate the various components according to the material they are made of in order to simplify reuse or differentiated disposal.
No particular operations are required after scrapping.
Do not dump the unit.
Take it to a disposal company.
Always comply with the current laws governing the scrapping of material in the country of use.
9.2 RESALE
If the unit is sold,hand over all the technical documentation to the new purchaser,inform him/her about any repair work carried
out and how to use and service the machine. Also inform Getidty.M.I.Co.ltd.of the sale and provide it with data about the new
purchaser.
Page 47 of 62
APPENDIX 1 Preparing the instruments for sterilization
A correct sterilization depends on the processes described below being carried out correctly; these are al lequally important
and, therefore, care must be taken while performing them.
1. Preparing the instruments to sterilize; 2. Packing; 3. Loading; 4. Sterilization;
5. Preserving the sterilized instruments; 6. Routine maintenance of the unit.
All the objects must be decontaminated and carefully cleaned and dried before being sterilized. In the case of instruments
with parts that are joined to each other, divide the parts or open them as wide apart as possible.
In the case of overalls or other reusable fabrics, these must be washed and dried after use and before sterilization,to remove
organic material and lengthen the "life" of the fabric, restoring it with its natural watercontent (i.e. degree of humidity).
The objectives of the initial decontamination procedure are as follows:

a) inactivating bacterial proliferation; b) preventing mutual contamination while handling instruments;
c) preventing any products present on the instrument from drying up; d) protecting personnel
Decontamination is carried out using detergents and, generally, solutions that are active against HIV, HBV and HCV,or by
washing at 93 °C for ten minutes in thermo-disinfectors. Observe the indications given in thetechnical data sheets of the
products used.
The instruments are cleaned so as to eliminate blood, saliva,dentin and organic substances in general, that may damage the
materials to be sterilized or even the sterilizer itself.The use of ultrasound baths isrecommended,which offer numerous
advantages with respect to traditional cleaning methods, such as efficacy,speed and delicacy on the object being cleaned;
always follow the recommendations provided by the respective manufacturers. In general, after ultrasound cleaning with
detergent and/or disinfectant,rinsing the instrument is recommended, in that the disinfectant may take on corrosive chara-
cteristics as a result of the heat.
Always clean the solution carefully to avoid residues of moisture.Once dry, the instruments to be sterilized in the unit must be
appropriately packaged, whereas those to be cold sterilized must be immersed in the appropriate chemical solution (glutara-
ldehyde, paracetic acid, etc.).
Checking the instruments to be used is also important: ensure that devices with the following characteristics are not subject
to sterilization:
- breaks
- stains
- rust
- mono-use devices that cannot be reused
Page 48 of 62
APPENDIX 2 Packaging
The correct packaging of the materials is essential in ensuring that sterility is maintained.Packaging of the instruments is done
so as to maintain the materials sterile until the time of their use.
The way in which the sterilized instruments are packaged, and then stocked, determines the state of preservation of sterilization.
The following can be used as containers: metal containers with lids or perforated bottoms with filters in paper, pouches in paper
or polypropylene,Medical Grade paper or trays that are perforated or with grilles.
Pouches in paper-polypropylene are excellent packaging systems for steam sterilizing small sets of surgical instruments or
individual instruments.
Use materials that comply with EN868-1 for packaging the materials to sterilize.
Do not re-sterilize the pouches in paper-polypropylene and the Medical Grade,in that they undergo a substantial
change in their structural characteristics and would no longer guarantee the characteristics of "protective barrier".
For packaging, observe the following recommendations (for pouches in paper-polypropylene):

1. Contents must not exceed ¾ of the volume of the pouch
2. The instruments must be positioned so that they can be extracted by their handle
3. The sealing strip on the pouch must be continuous with a height of at least 6mm (UNI EN 868-3).
Each package prepared must at least indicate the date of sterilization, the type of cycle performed and the date in which the
preservation of sterility expires; this latter value must be established considering the length of preservation of sterility as
indicated by the manufacturer of the packaging material,the internal procedure used and the stocking conditions of the
sterilized material itself.
Instruments packaged in individual pouches have a life (in terms of sterility) of 30 days, those in double pouches of 60, if
kept in closed cabinets.These values are,in any case,to be considered indicative,in that the date of preservation is influenced
by various factors,such as the environmental microbic level,the granulometry of environmental dusts (that act as carriers of
micro-organisms),as well as the temperature, pressure and ambient humidity parameters and the degree of handling of the
sterilized material.
Packaging methods that make it possible to avoid partial withdrawals and that allow for mono-patient use are optimum.
Page 49 of 62
APPENDIX 3 Positioning the load
The way in which the load to sterilize is arranged is also considerably important to the sterilization process.Always observe
the maximum load indicated in this manual,a value that has been tested by the manufacturer and that is therefore valid.
- Always use the tray supports, to facilitate the circulation of steam.

-Do not load trays that are not being used.
-Load the unused trays in an upside down position, to avoid any accumulation of water in the boiler.
-Where it is necessary to sterilize loose instruments, it is advisable to cover the tray with sheets of Tray Paper to avoid any
direct contact of the instruments with the tray.
-Ensure that instruments of different materials are separated and placed on different trays.
-For improved sterilization,open instruments such as pincers,scissors,or other composite instruments.
-Position the instruments sufficiently distant from one another that they remain separate for the whole sterilization cycle.
-Do not stack instruments on the tray: overloading could compromise sterilization.
-Mirrors should be placed glass side down.
-Do not stack the trays on top of each other,but use the tray support.It is necessary to leave a space between each tray to allow
for the circulation of steam during the sterilization phase and then to facilitate drying.
-Place a chemical sterilization indicator on each tray.
- Tubes
After the tubes have been cleaned normally, rinse them using water without pyrogene.
Place them on the tray so that the two ends are open and so that they do not bend or twist.
- Packages
Place the packages upwards, next to each other, do not allow them to come into contact with the sides of the chamber.
- Material in pouches
When sterilizing material in pouches, do not overlap the pouches on the trays (Fig. A3-1).
Place the pouch with the transparent side face down (in contact with the tray) and with the paper face up (Fig. A3-2).
Instruments must be put into separate pouches.
Page 50 of 62
After following the instructions above, put the tray holder and trays into the sterilization chamber.
WARNING: insert the tray support and the trays, paying particular attention not to damage the door gasket.
APPENDIX 4 Unloading and preserving sterilized instruments

The material is at the greatest risk of contamination while it is still hot,because the barrier capabilities of the packaging
materials are much lower in the presence of residual humidity,compared to an ambient temperature situation.The materials,
therefore,should not be stacked once they have been extracted, in order to favour the dispersion of heat.
Wait for the material to drop to room temperature before stocking it: before stocking, make sure that the packages are
intactand check the chemical colour change;if the package is broken or torn,the load can only be used immediately,in that
preservation of sterility cannot be guaranteed.
The indicative times for preserving the material are shown below, considering that the material itself is kept in closed cabinets
away from light, heat and humidity.
Type of material Suggested time (in days)
Combination of paper-polypropylene 30 (single) - 60 (double)
Metal containers, with standard-grade filters 28/30

Medical Grade with double orthogonal layer 28/30
Page 51 of 62
The material should be stocked in sealed cabinets, 30 cm away from the floor and 5 cm from the ceiling; if this is not possible,
protect the material in nylon bags.
We emphasize the fact that the times indicated in the table above are indicative, in that the preservation of
i sterility depends on numerous factors, such as the ambient microbic level, the size of the dust particles, the
ambient conditions of temperature, pressure and humidity, as well as the degree of handling of the sterilized
materials themselves.
APPENDIX 5 Description of programs
134 -03m-1times
PROGRAM LIST
Vacuum times
1. Prompt 134 !"# 03m-1Times
2. Solid 134 !"# 04m-1Times Sterilization time
3.Hollow 134 !"# 04m-3Times Sterilization temperature
4.Sanguinary134 !"# 18m-3Times
121- !" 20m-1Times
5.Solid Operation.
6.Hollow 121 !"# 20m-3Times
HELP Press KEY. JQ-A-18 JQ-A-23
7.Glass 121 !"# 20m-1Times
8.Tampon 121 !"# 30m-3Times Maximum load: Solid 4.5kg 6.0kg
Porous 1.5kg 2.0kg
Page 52 of 62
P
V1 1st vacuum
P1 1st pressure rise
STS STE V2 2nd vacuum
P3 DS Pre-Vacuum
P1 P2 P2 2nd pressure rise
V3 3rd vacuum
DE P3 3rd pressure rise
STS Start of sterilization period
V1 V2 V3 Sterilization
t STE End of sterilization period
Pre-Vacuum Drying
DS Start of drying phase
Pre-Heating Sterilization Drying
DE End of drying phase
The individual sterilization cycles are now described below: due to their all being class B, they can sterilize all kinds of load,
be it porous, solid or hollow.In all cases, the recommendations given by the manufacturer regarding sterilization
methods and times should be followed.
Program 6 Hollow (121 -20m-3times)
This program is used to sterilize objects that are sensitive to temperature, as well as rubber,some articles in plastic in open
trays, or appropriate perforated trays.
Hollow instruments and dental instruments such as tubes and similar objects can also be sterilized,after making sure that
they have previously been cleaned, disinfected and rinsed. The objects indicated above can also be sterilized without the use
of pouches.
This program is particularly suited for sterilizing products in pouches (both single and double pouches),products that will
have to be kept sterile for a long period of time.
The length of this cycle depends on the weight of the load, on the type of load and on the temperature in the chamber upon
start-up of the cycle.
Page 53 of 62
Program 8 Tampon(121 -30m-3times)
This program is specialized in the instruments of cotton,fabrics wich also sensitive to temperature,in open trays or appropriate
perforated trays.
Hollow instruments and dental instruments such as cotton and similar objects can also be sterilized,after making sure that
they have previously been cleaned,disinfected and rinsed. The objects indicated above can also be sterilized without the use
of pouches.
This program is particularly suited for sterilizing products in pouches,products that will have to be kept sterile for a long
period of time.
The length of this cycle depends on the weight of the load,on the type of load and on the temperature in the chamber upon
Program 3 Hollow(134 -04m-3times)
This program can be used both to sterilize solid instruments in open trays or using the specific perforated trays.Loads arranged
both in single and in double pouches can be sterilized.
they have previously been cleaned,disinfected and rinsed. The objects indicated above can also be sterilized without the use
of pouches.
This program is particularly suited for sterilizing products in pouches,products that will have to be kept sterile for a long
period of time.
The length of this cycle depends on the weight of the load,on the type of load and on the temperature in the chamber upon
Program 4 Sanguinary(134 -18m-3times)
This program is used to sterilize instruments suspected to have been contaminated by prions.The program makes it possible
to sterilize articles, packed in single or in double pouches, in open trays or in specific perforated trays.
they have previously been cleaned, disinfected and rinsed.
The objects indicated above can also be sterilized without the use of pouches.
This program is particularly suited for sterilizing boxes of products in pouches, products that will have to be kept sterile for a
long period of time.
The length of the cycle depends on the weight of the load, on the type of load and on the temperature in the chamber upon
Page 54 of 62
APPENDIX 6 Description of Tests
It is important to periodically verify the performance of the unit by performing the appropriate tests; JQ-A series can
perform three different ones:
--B&D test -- Vacuum test -- Helix test
The frequency at which these tests should The parameters of the respective cycles are as follows:
be performed is indicated below:
Parameter cycles Vacuum Test B&D Test Helix Test
Vcauum Test Monthly Temperature ---------- 135.5 135.5
B&D Test Daily Pressure -0.880bar 2.16bar 2.16bar

Sterilization ---------- 3’30” 3’30”
Helix Test Daily
Drying ---------- 20’ 20’
Vacuum Test
This test is performed in order to check the performance of the unit, in particular:
- the efficiency of the vacuum pump;
-the seal of the pneumatic circuit. P
The cycle is structured as follows:
1. a vacuum is created up to -0.880 bar t1 t2 t3 t4
2. this pressure is maintained for 5 minutes and then measured
3. pressure is maintained for 10 minutes and then measured t
4. Pressure in Chamber balance with the air pressure,2 min.
®
In compliance with EN13060, the test requires a tightness test of

less than or equal to 1.3 mbar/min during the 10 minutes of test;
if the leakage is greater than this value, the outcome of the test -0.880bar
is negative; the seal of the pneumatic circuit of the device must P2 P3
be checked.
P1
Page 55 of 62
In order to achieve a correct result, the test must be carried out with the unit cold, i.e.within 3
minutes from machine start-up.
Bowie & Dick test
This is a chemical-physical test that is also known as the Brown test: the indicator is a heat-sensitive sheet that is placed in
the middle of a packet made up of various layers of paper and foam rubber.
The B&D test simulates the performance of the unit with regard to P
the sterilization of porous loads, in particular:
--the efficiency of the preliminary vacuum and the penetration of steam
within the pores; STS STE
P3 DS
--the temperature and pressure values of the saturated steam during P1 P2
the sterilization phase.
The packet for the B&D test must be inserted on its own, preferably on the DE
lowest tray, with the label facingup.
After performing the cycle, specifically the 134 cycle, immediately verify
the test. Being careful while handling V1 V2 V3
the packet (it is still hot), remove the indicator sheet and follow the instr- t
Pre-Vacuum Drying
uctions given in the package for evaluating the result of the test.
Pre-Heating Sterilization
Helix test
The Helix test represents a hollow A-type load, i.e. the load with themost critical
characteristics.
The test consists of a tube in polytetrafluoroethylene (PTFE)with a length of 150mm and
internal diameter of 2mm.
The Helix test simulates the performance of the unit with respect to the sterilization of
hollow loads,in particular:
--the efficiency of the preliminary vacuum and the penetration of steam within the pores;
--the temperature and pressure values of the saturated steam during the sterilization phase.
Page 56 of 62
P
WARNING: carry out the Helix test only after a
STS
P3
STE
DS sterilisation cycle.
P1 P2
DE After placing the strip in the capsule, position the tube on the lowest
tray inside the sterilization chamber.
V1 V2 V3
t
At the end of the cycle, take the tube out immediately (with care in
Pre-Vacuum Drying that the load is still hot)and verify the result of the test,referring to the
Pre-Heating Sterilization indications given on the package.
APPENDIX 7 Validating the cycles
With reference to standard EN 13060, the following cycles have been validated:
134 -04m-3times 134 -18m-3times 121 -20m-3times
Dynamic pressure of the
chamber of the sterilizer
Air leakage
Empty chamber
Solid load
Small porous articles
Light porous loads
Full porous loads
Hollow load B
Hollow load A
Multiple packaging
Dryness, solid load
Dryness, porous load
Page 57 of 62
A number of definitions that are of use in understanding the table above follow:
--Solid load: non-porous article, without notches or other characteristics that may hinder the penetration of steam in an equal
or greater amount than those of a hollow load.
--Porous load: material that is capable of absorbing fluids; in particular this regards:
A . a full porous load when the load occupies 95 ±5 % of the usable space.
B . a light porous load when the load occupies 20-25% of the usable space.
C . a small porous load when the load occupies 0.5-5% of the usable space.
--Hollow load A :space open at one end in which 1 L/D 750,where D is the diameter of the cavity and L the length,with L
1500mm,or space open at both ends in which 2 L/D 1500, with L 3000mm and that is not hollow load B.
-- Hollow load B : space open at one end in which 1 L/D 5, where D is the diameter of the cavity and L thelength, with D
5mm, or space open at both ends in which 2 L/D 10, with D 5mm.
APPENDIX 8 Quality of process water Inlet water Condensate

Evaporated residue < 10 mg/l <1 mg/l
With reference to standard EN 13060,the table below Silicon oxide 1 mg/l 0. 1 mg/l
indicates the recommended limit values (maximum)
for contaminating agents, as well as the chemical- Iron 0.2 mg/l 0.1 mg/l
physical characteristics of the water used for condensate Cadmium 0.005 mg/l 0.005 mg/l
and inlet water. Lead 0.005 mg/l 0.05 mg/l
Condensate is produced by the steam that was formed by Heavy metal residues 0.1 mg/l 0.1 mg/l
the empty chamber of the sterilizer. Chlorides 2 mg/l 0.1 mg/l
Phosphates 0.5 mg/l 0.1 mg/l
The use of water for generating steam cont- Conductivity at 20°C 15 µS/cm 3 µS/cm
aining contaminants at higher levels than PH 5-7 5-7
those shown in this table may considerably
shorten the working life of a sterilizer and Appearance colourless,clean,sediment-free
may invalidate the maker's guarantee. Hardness 0.02 mmol/l
Page 58 of 62
APPENDIX 9 Troubleshooting
The table below lists all the alarm messages with the probable causes of faults; whenever your display shows a screen of this type,
before calling the technical assistance service, perform the operations indicated.
Alarm Cause
Temperature sensor
(steam generator)
01 is broken!
Alarm Code Program what kind of phases
the problem happen?
<134>
00:24
42.3 This date just some codes for
-0.286bar problem,the engineers of getidy
41.5 M.I.co.,ltd.,can judge the problem
0902-3403-94110516 according this code.
0000-0004-28000000
0812-1300-00000013
Alarm Code Alarm Cause Solution

00 Abnormal Exiting! According the Chap7.10 Abnormal Exiting operate.
Temperature sensor(steam replaceTemperature sensor(steam generator)

01
generator)is broken!
Page 59 of 62
Alarm Code Alarm Cause Solution
Temperature sensor(Out
02 Chamber) is broken! -Replace Temperature sensor(Out Chamber).
Temperature sensor(In -Replace Temperature sensor(in Chamber).

03 Chamber)is broken!
-Check for any leakages.

04 Sterilization failed! -Reset the safety thermostat. -Check the generator resistance.
--Sterilization over and Exhaust:check the Ev1 opening.part of hydraulic circuit if be

Pressure can not be
05 clogged?.--Drying and balance air:check Ev4 opening.check air filter if not be clogged?
exhausted!
check part of hydraulic circuit if be clogged?
Door is opened in the -Check if the door be closed or not?

06 working! -Check the structure of get door message if necessary chang it..
-Check the integrity of thegenerator resistance.

07 Operation time over! -Reset the safety thermostat. -The generator be clogged,clean it.
08 Pressure over! -Check and if necessary adjust the calibration of pressure sensor.
09 Temperature over! -Check and if necessary adjust the calibration of temperature sensor.
Pressure and Temperature

10 do not match! -Check the any leakages on hydraulic circuit.
11 Electric-lock not moving! -Adjust and if necessary change it.
12 Vacuum process failure! -Check for any leakages from the pneumatic circuit.-check the vacuum pump.
Page 60 of 62
liquor sensor
(side type)
Liquor sensor Heating loop
(stand type)
Ev1
Solenoid Valve
fan (Opened )
Ev6
filter Solenoid Valve

(0~1bar)
Ev3
Solenoid Valve Transformer Ev5
Electromagnetic lock Vcauum pump
(Vacuum pump )
Solenoid Valve
(Drain water)
deflation
Solenoid Valve Solenoid Valve
Steam generator Water pump (Air filiter ) (Water pump )
condenser Ev4 Ev2
safety valve
APPENDIX10 Components graph of
whole machine
fuse To printer
Page 59 of 62
Page 60 of 62 APPENDIX 11 Hyhranlic Circuit
Pressure sensor
Solenoid valve Safety valve
(Opened)
Ev1
Solenoid valve
(drain water)
Ev5
Radiator Solenoid valve

(water pump) Solenoid valve
Ev6 (Air filter)
Ev4
Solenoid valve
(0~1bar) Ev2
Solenoid valve
(Vacuum pump)
Steam Ev3 Air filter

generator
Chamber Vacuum pump
Water pump
Clean water tank
Water discharging
vavle
Used-water tank
Water discharging
vavle

Autoclave Getidy

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Autoclave Getidy

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CONTENTS

Sheet for rapid use....................................................................................... .............................. ..Enclosure

The boiler complies with the following standards: EN 13445:2002.

2.2 STAFF REQUIREMENTS

2.3 USING AND STORING THE MANUAL

2.4 READING THE MANUAL: SYMBOLS AND CONVENTIONS

i INFORMATION AND PRECAUTIONS

2.5 HOW TO OBTAIN A NEW COPY OF THE MANUAL

Send your request to the following address:

Zhejiang Getidy Medical Instrument Co.,ltd

3.2 INTENDED USE

3.3 SAFETY DEVICES

Double-pole thermal safety switch for protecting

Protection of the electronic board against

Mechanical safety devices

Door lock micro-switch: shows the correct position of the

3.4 RESIDUE RISKS

Fig. 3.4-1 Fig. 3.4-2

ATTENTION: Hot surface.

These signs must not be removed, covered or damaged.

3.6 PERSONAL PROTECTIVE EQUIPMENT (PPE)

4. Receipt and handling

Overall dimensions of packaging

4.3 DESCRIPTION OF CONTENTS

Description Specifications Quantity

4.3.1 Optional devices

External memory U Disk(1GB) 1

i JQ-A series Autoclave:

5.1.1 Front elements

2. Handle for opening the door.

6. Connector for draining clean-water. Fig. 5.1.1-1

Devices on the front of the unit with the door open 8

5.1.2 Rear elements

575 300 580 5

Overall dimensions of the machine with door closed

"WARNING, READ THE INSTRUCTIONS MANUAL"

5.4 EXTERNAL PRINTER

Use rolls of thermal printer paper with the following characteristics:

--The unit should be installed inside a laboratory,

6.2 INSTALLING THE UNIT

ATTENTION: the unit MUST be installed by specialised technicians.

ATTENTION: Once installed and connected to an electrical power point,

ATTENTION: Electrical connections must be made by specialised technicians.

Only use the original lead.

6.4 FIRST START-UP

Filling with distilled water for the first time

USB PRINTER USB PRINTER

Emptying used water PROMPT

NEVER REUTILISE USED WATER.

Never exceed the max. load specified in Appendix 5 "Description of Programs".

7.1.1 Trun on.After pressing the switch ON-OFF

7.1.3 load the material

Before starting the selected cycle,load the

--open the door.(Fig.7.1.3-1) Fig.7.1.3-1

7.2 SELECTING A STERILIZATION CYCLE PROGRAM PROGRAM LIST

PROMPT Fig.7.2-1 Fig.7.2-2

7.4 TEST PROGRAM

05:00 05:00 10:00 00:00

Fig.7.4.1-1 Fig.7.4.1-2 Fig.7.4.1-3 Fig.7.4.1-4 Fig.7.4.1-5 Fig.7.4.1-6

7.5.1 Time Set Time Set

Fig.7.8-6 Fig.7.8-7 Fig.7.8-8 Fig.7.8-9 Fig.7.8-10

After sterilization, Beginning of Readin to U disk or The sterilization

7.10 Abnormal Exiting