DC30-006 Quantum QT-740 & QT-750 Operator Manual Rev G

™
Models QT-740 and QT-750

Fixed/Elevating
Float-Top
Radiographic Tables
Operator’s Manual
Manual Part No. DC30-006 Revision G

This manual is copyrighted and all rights are reserved. No portion of this document
may be copied, photocopied, reproduced, translated, or reduced to any electronic
medium or machine readable form without prior consent in writing from Quantum
Medical Imaging, LLC. (QMI)
Copyright© 2009 QMI
Quantum Medical Imaging, LLC Made in U.S.A.

2002-B Orville Drive North
Ronkonkoma, New York 11779 USA
Phone: (631) 567-5800
Fax: (631) 567-5074
E-mail: info@qmiteam.com
www.quantummedical.net
Revision History
REVISION DATE TYPE OF MODIFICATION

A 12/08/00 Initial Release.
B 3/14/01 Incorporated ECO 0245
C 5/17/01 Added UL mark
D 4/30/04 Incorporated ECO 1359
E 5/2/06 Incorporated ECO 1583
F 9/16/09 Incorporate ECO 2123, 2173, 2199, and updated

CE mark
G 10/27/09 Incorporate ECO 2011, 2092
Page Page Page

Number Rev Number Rev Number Rev
i - iv G
1-1 thru 1-6 G

2-1 thru 2-4 G
3-1 thru 3-14 G
4-1 thru 4-4 G
5-1 thru 5-8 G
Models QT-740 & QT-750 - Operator’s Manual Revision G

Quantum Medical Imaging, LLC i
Revision History
THIS PAGE INTENTIONALLY LEFT BLANK
Revision G Models QT-740 & QT-750 - Operator’s Manual

ii Quantum Medical Imaging, LLC
Table of Contents
Table of Contents
Chapter 1, Safety Notices 1-1
Chapter 2, General Information 2-1
Chapter 3, Operation 3-1
Chapter 4, User Maintenance 4-1
Chapter 5, Warranty Information 5-1

Quantum Medical Imaging, LLC iii
Table of Contents

iv Quantum Medical Imaging, LLC
Chapter
1
SAFETY NOTICES
1-1
1-2
Chapter 1 Safety Notices
GENERAL SAFETY INFORMATION

Follow the safety instructions in this manual and all warnings and cautions printed on
the warning labels. This manual, along with system components’ manuals, must be
read and understood before using the system. Below is a definition of the warning
signs used throughout this document:
WARNING Indicates injury or death is possible if the

instructions are not obeyed.
Indicates that damage to equipment is possible
CAUTION if the instructions are not obeyed.
NOTE Indicates essential information that should be

read to avoid incorrect operation.
WARNING
Quantum Medical Imaging, LLC disclaims all responsibility from any injury
resulting from improper application of this equipment.
This equipment is sold to be used exclusively under the prescribed direc-
tion of a person who is licensed by law to operate equipment of this nature.
This equipment must be used in accordance with all safety procedures
described in this manual and must not be used for purposes other than
those described herein.
Quantum Medical Imaging, LLC cannot assume responsibility for any mal-
functioning of this equipment resulting from improper operation, mainte-
nance, or repair, or from damage or modification of its components.
X-RAY PROTECTION
X-rays are hazardous to both patient and operator unless established safe
exposure factors and operating instructions are observed.
It is important that everyone having anything to do with x-radiation be
properly trained and fully acquainted with the recommendations of the
National Council on Radiation Protection and Measurements as published

Quantum Medical Imaging, LLC 1-3
in NCRP Reports available from NCRP Publications, 7910 Woodmont Ave-

nue, Suite 800, Bethesda, Maryland 20814-3095 (www.ncrp.com), and of
the International Commission on Radiological Protection (www.icrp.org),
and take adequate steps to protect against injury.
X-ray equipment may cause injury if used improperly. The instructions con-
tained in this manual must be read and followed when operating this unit.
Personal radiation monitoring and protective devices are available. You are
urged to use them to protect against unnecessary x-ray exposure.
REGULATORY COMPLIANCE
This certified Quantum Medical Imaging, LLC medical device has been designed,
manufactured, and calibrated to comply with governing Federal Regulations 21 CFR
Subchapter J and the performance standards attendant thereto. Upon installation, all
certified products require the filing of Form FD-2579 "Report of Assembly of a Diag-
nostic X-ray System" by the assembler (i.e., the installer) with the appropriate agen-
cies; the "Installation Quality Assurance Checklist" must also be completed and
properly distributed upon installation. A copy of each form (pink copy) is provided to
the user. The installation report is completed by the installer and returned to Quan-
tum Medical Imaging, LLC.
Those responsible for the planning of x-ray equipment installations must be thor-
oughly familiar and comply completely with NCRP Report No. 49, "Structural Shielding
Design and Evaluation for Medical Use of X-Rays and Gamma Rays of Energies up to
10 MeV", as revised or replaced in the future. Those authorized to operate, test, par-
ticipate in or supervise the operation of the equipment must be thoroughly familiar
and comply completely with the currently established safe exposure factors and pro-
cedures described in publications such as Subchapter J of Title 21 of the Code of Fed-
eral Regulations, "Diagnostic X-Ray Systems and Their Major Components," and NCRP
Report No. 102, “Medical X-Ray, Electron Beam and Gamma Ray Protection for Ener-
gies Up to 50 MeV—Equipment Design and Use” as revised or replaced in the future.
Scheduled maintenance is essential to the assurance of continued integrity of this
equipment with respect to regulatory compliance. The continuance of certified perfor-
mance to the regulatory standard is incumbent upon the user's diligent conformance
to recommended maintenance instructions.
This product has been classified as Class I, Type B by Underwriters Laboratories, Inc.
Equipment not suitable for use in the presence of a flammable anesthetic mixture
with air or with oxygen or with nitrous oxide.
MEDICAL ELECTRICAL EQUIPMENT

WITH RESPECT TO ELECTRIC SHOCK, FIRE,
MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH
UL 60601-1 AND CAN/CSA C22.2 NO. 601.1
98UA

1-4 Quantum Medical Imaging, LLC
EU Authorized Representative:
Medizintechnik Berlin GmbH
Altentreptower, Strasse 59
12683 Berlin - Germany
Phone: +49-302-82 4726
Fax: +49-302-82 6382
E-mail: Medizintechnik.Berlin.GmbH@t-online.de
The following symbols may be used for marking on this equipment or equipment doc-
umentation:
Earth (ground) Type B Equipment
Protective Earth (ground) Attention, consult accompanying

documents
Dangerous Voltage Enable tabletop float (releases

transverse and longitudinal locks)
Enable Tabletop Up Motion Enable Tabletop Down Motion
ASSOCIATED DOCUMENTS
This Operator’s Manual is incomplete without QT-740 & QT-750 Fixed/Elevating Float-
Top Radiographic Tables Service Manual, document number DC30-007.


Chapter
2
GENERAL
INFORMATION
2-1
2-2
Chapter 2 General Information
OVERVIEW
This manual provides information for installing, operating, and maintaining Quantum
Medical Imaging’s Fixed (Model QT-740) and Elevating (Model QT-750) Radiographic
Tables (hereinafter referred to as the radiographic table). It is imperative that all
NOTE safety procedures described in this manual be strictly adhered to in order to ensure
the safety of both patient and user.
The user should
read this man- The key features of Model QT-740 and QT-750 radiographic tables are as follows:
ual in its en-
tirety prior to • Large Tabletop area (85 inches long x 35.55 inches wide) provides ample
using this equip- examination platform
ment. It should
be kept in a • Four-way floating tabletop permits 30.5 inches of longitudinal travel and 10
location near inches of lateral travel for full radiographic coverage
the equipment
and readily ac- • Foot pedal controls for table float-top motions (foot pedal inhibit switch
cessible to the deactivates foot pedals to prevent inadvertent tabletop motion)
those that oper-
ate it.
• Float Handle Assembly with FLOAT push button control is provided for
operator convenience
• Small patient-to-film plane distance provides improved radiography with
minimal magnification
• Accepts all types of image receptors (buckies, grids, and stationary grid
cabinets)
• Patient handgrips are standard accessory
• AC line cord, fitted with hospital-grade plug, plugs into a 115VAC, 50/60 Hz
receptacle (optionally field wired). Also configurable for 230 VAC, 50/60 Hz
power input.
• The Image Receptor Cabinet is equipped with electric locks ensuring precise
film receptor alignment
In addition, the Model QT-750 provides:
• Heavy-duty lift mechanism allows for patient loads of up to 650 lbs.* (weight
must be centered over table base)
• Variable height tabletop, lowers to 21 inches and raises to 32.5 inches (11.5
inches total vertical travel)
• Foot pedal and hand controls for table up/down motions
• Obstruction sensors disable tabletop down motion in the event an
obstruction is detected below tabletop
* 600 lbs. capacity when table is equipped with QT-FCD (Fixed Digital Image
Receptor) option; 550 lbs. capacity when equipped when table is equipped with
QT-DDS (Digital Drawer Slide) option.
INTENDED USE
The Fixed Float-top (Model QT-740) and Elevating Float-top (Model QT-750)
Radiographic Tables are intended for use as a patient support device during the
performance of radiographic examinations.

Chapter 2 General Information
MAIN COMPONENTS
See Figure 2-1. The radiographic table contains:
1 Patient Handgrips
2 Tabletop
3 Image Receptor Lock Release Switch
4 Control Handle: FLOAT Push Button Switch
5 Control Handle: UP/DOWN Rocker Switch (Model QT-750 only)
6 Foot Pedal(s) - Float (Model QT-740)
Float, Up and Down (Model QT-750)
7 Table Base
8 Foot Pedal/FLOAT Push Button Inhibit Switch
9 Emergency Shut-off Switch (Model QT-750 only)
1 2 3 4 5
8 6
Figure 2-1. Radiographic Table Main Components

Chapter
3
OPERATION
3-1
3-2
Chapter 3 Operation
OVERVIEW
To provide precise patient positioning, Models QT-740 and QT-750 radiographic
tables feature a table top that "floats" in four directions; transversely (forward
and backward) and longitudinally (left and right). Model QT-750 has the addi-
tional capability of table top elevation (i.e., the table top can be raised and low-
ered to facilitate easy transfer of the patient onto and off of the table top).
TABLE CONTROLS
WARNING! All movable assemblies and parts of
this equipment must be operated with reasonable
care. Manufacturer’s equipment recommenda-
tions described in this manual must be observed.
WARNING! To avoid damage to the table, any

load on table top should be distributed as evenly
as possible over the support surface. Do not seat
patient at extreme ends of table top when table
top is not centered. Patients weighing more than
approximately 300 lbs. (136 kg) should only be
transferred on or off the table from front side - in
the center.
WARNING! Do not allow patient to place his/her

hands along the side or below the table rail.
Injury to the patient’s hands and/or fingers is
possible.
TABLE TOP FLOAT MOTION (ALL MODELS)

Models QT-740 and QT-750 both feature a "floating" table top. With the "float-
ing" table top function activated, both transverse and longitudinal positioning of
the patient is enabled. To operate the float-top function, proceed as follows:
WARNING! When transferring a patient on or off

the table top, always make sure the table top is
locked. If necessary, the Foot Pedal Disable
Switch may be activated to prevent unintended
activation of the FLOAT Foot Pedal control.

Chapter 3 Operation
1. Position the patient on the table with his or her hands situated along the side
of their body, or with the hands grasping the patient handles (see Figure
3-1). Be sure that the hands remain above the table top.
Figure 3-1. Patient Positioned on Table Top

2. Press the FLOAT Foot Pedal or the FLOAT push button on the Table Control
Handle to enable transverse and longitudinal motion of the table top (see Fig-
ures 3-2 through 3-4).
FLOAT Foot Pedal
Figure 3-2. Model QT-740 FLOAT Foot Pedal Control

Chapter 3 Operation
3. Releasing the FLOAT Foot Pedal or the FLOAT push button (located on the
Table Control Handle) immediately activates the table top locks, thereby
inhibiting table top "float" motion.
FLOAT Foot Pedals
Figure 3-3. Model QT-750 - FLOAT Foot Pedal Controls
TABLE TOP FLOAT

ENABLE PUSH BUTTON
MODEL QT-740 MODEL QT-750
Figure 3-4. Table Control Handle FLOAT Push Button Switch

Chapter 3 Operation
FOOT PEDAL/CONTROL HANDLE DISABLE SWITCH (ALL MODELS)

To prevent accidental activation of both the Foot Pedal controls (i.e., FLOAT Foot
Pedal on Model QT-740 and FLOAT, UP, and DOWN Foot Pedals on Model
QT-750) and the Control Handle push buttons, a Foot Pedal/Control Handle Dis-
able Switch is provided. This switch is located below the front table rail on the
left end of the table (see Figure 3-5). Pressing the switch until the switch light is
illuminated disables all Foot Pedal and Control Handle functions. Pressing the
switch until the Foot Pedal/Control Handle Disable Switch light is not illuminated
restores normal operation of both the Foot Pedal and Control Handle switches.
.
FOOT PEDAL/
CONTROL HANDLE
PUSH BUTTON
DISABLE SWITCH
Figure 3-5. Foot Pedal/Control Handle Disable Switch Location

Chapter 3 Operation
ELEVATING MOTION (MODEL QT-750 ONLY)

On Model QT-750 radiographic tables, the elevation function allows the table top
NOTE
to be lowered down to as low as 21 inches (533.4 mm) from floor, up to a work-
ing height of 32.5 inches (825.5 mm). To operate the table top elevation func-
The Model QT-
750 table is tion, proceed as follows:
equipped with
Obstruction WARNING! For safety purposes on Model
Sensors, which QT-750 tables, an Emergency Stop Switch (see
detect the Figure 3-6) when activated immediately removes
presence of an
obstruction power from the table top up/down motor. Rotat-
below the table ing the Emergency Stop Switch knob 1/4-turn
top when the counter-clockwise releases the Emergency Stop
table top is Switch and restores up/down motor power.
being driven
downward.
This feature is
only designed
to avoid dam-
age to the
table and is not
intended as a
safeguard
against per-
sonal injury.
EMERGENCY STOP
SWITCH
(MODEL QT-750 ONLY)
Figure 3-6. Emergency Stop Switch Location
IMPORTANT! On Model QT-750 tables equipped

with Digital Receptor Drawer Slide Option (QT-
DDS): Table top up or down motion is disabled
when the digital receptor drawer slide is
extended out from under the table top. Push
receptor in fully to enable up or down motion.

Chapter 3 Operation
DOWN PEDAL UP PEDAL
Figure 3-7. Model QT-750 - Up/Down Foot Pedal Controls
PRESS HERE TO ENABLE

TABLE TOP UP MOTION
PRESS HERE TO ENABLE

TABLE TOP DOWN MOTION
Figure 3-8. Model QT-750 - Control Handle Table Top Up/Down Rocker Switch
LOWERING THE TABLE TOP
1. It is recommended that the table top be centered before lowering
it (refer to table top Float Motion operation described in preced-
ing paragraph).
2. Press the DOWN Foot Pedal (see Figure 3-7) or, on the Control
Handle (see Figure 3-8), press the Table Top Rocker Switch
toward the down arrow to lower the table top to the desired
height.
3. Transfer patient onto table top.

Chapter 3 Operation
4. Ensure patient is positioned with his or her hands situated along

the side of their body, or with the hands grasping the patient
handles (see Figure 3-1). Be sure patient’s hands remain above
the table top.
RAISING THE TABLE TOP
1. Press the UP Foot Pedal (see Figure 3-7) or, on the Control Han-
dle (see Figure 3-8), press the Table Top Rocker Switch toward
the up arrow to raise the table top to the desired height.
2. Proceed with examination.
IMAGE RECEPTOR CABINET LOCK
The Image Receptor Cabinet rides on four linear ball-bearings mounted to adjust-
able brackets attached to either side of the cabinet. These bearings travel on the
hardened and polished steel shafts of the Receptor Cabinet Carriage. An electro-
magnet on the underside of the housing "locks" the cabinet into place until the
LOCK RELEASE switch is depressed, thereby releasing the magnet’s hold and
allowing free movement of the cabinet (see Figure 3-9).
LOCK RELEASE
SWITCH
Figure 3-9. Image Receptor Cabinet LOCK RELEASE Switch

CASSETTE TRAY OPERATION
The radiographic table is equipped with either a Midwest or Poersch cassette tray,
depending on the system ordered. The following paragraphs describe the operat-
ing instructions for each. Additional information is contained in the cassette tray
manufacturer’s documentation, which is provided with the table.

Chapter 3 Operation
Loading Cassette Tray (Midwest Type)

To load a film cassette into a "Midwest" type cassette tray, proceed as fol-
lows:
1. Float the table top fully back.
2. Pull cassette tray from receptor using tray handle (see Figure
3-10).
3. Pull back on front cassette grip to open both grips.
4. Position slide guides ("L" brackets seated in channels) to cassette
size using indicators on cassette tray (press center brass button
to allow movement).
5. Insert cassette into tray (back end first).
6. Lock cassette into tray.
7. Push front grip against cassette.
8. While pushing front grip against cassette, turn cassette lock han-
dle to lock position.
9. Push tray into receptor. The cassette is now in exposure position.
SLIDE GUIDES
CASSETTE GRIP
LOCK HANDLE
TRAY HANDLE
Figure 3-10. Midwest Cassette Film Tray

Chapter 3 Operation
Loading Cassette Tray (Poersch Type)

To load a film cassette into a "Poersch" type cassette tray, proceed as fol-
lows:
2. Pull cassette tray from receptor using tray handle (see Figure
3-11).
3. Place thumb under lip of clamp handle. Lift handle to release.
4. Grasp handle and slide clamp back for inserting cassette.
5. Insert cassette into tray (back end first). Center it using center-
ing label.
6. Slide clamp forward pushing clamp firmly against cassette.
7. While pushing clamp against cassette, press clamp handle down.
CLAMP HANDLE
TRAY HANDLE
Figure 3-11. Poersch Cassette Film Tray

Chapter 3 Operation
DIGITAL DRAWER SLIDE OPTION (QT-DDS) OPERATION

The following paragraphs describe operating instructions for the QT-DDS Digital
Drawer Slide option. For instructions pertaining to operation of the digital imag-
ing system, refer to the Digital Receptor manufacturer’s documentation provided
with the digital imaging system.
Digital Receptor (Stored)
RECEPTOR
LOCK HANDLE
Figure 3-12. Digital Image Receptor - Stored Position
WARNING! Keep fingers away from area between

top of receptor and table top when pushing in
receptor; fingers may get caught.
Lift up on the Receptor Lock Handle and push the receptor forward until
the receptor is fully withdrawn below the table top as shown in Figure
3-12.

Chapter 3 Operation
Digital Receptor (Extended)
RECEPTOR
LOCK HANDLE
Figure 3-13. Digital Image Receptor - Extended Position
WARNING! Do not apply a load of more than 32

lbs. (14.5 kg) on the image receptor when it is in
the extended position; the unit may be collapse.
WARNING! On Model QT-750 tables equipped

with Digital Receptor Drawer Slide Option
(QT-DDS): Table top up or down motion is dis-
abled when the digital receptor drawer slide is
extended out from under the table top. Push
receptor in fully to enable up or down motion.
Lift up on the Receptor Lock Handle and pull the receptor forward until
the receptor is fully extended as shown in Figure 3-13.
Digital Receptor Lateral (Left-to-Right) Motion
Lift up on the Receptor Lock Handle and slide the digital left or right until
the desired lateral receptor position is attained. Release the Receptor
Lock Handle to lock the receptor in its current position.

Chapter 3 Operation
CXDI-50G DIGITAL RECEPTOR CABINET OPTION (TYPE RT-DOK50-T) OPERATION

Quantum offers an optional, motorized, rotating receptor tray for use with a
Canon CXDI-50G digital receptor used in QT-740 and QT-750 X-ray table applica-
tions. The RT-DOK50-T option provides a rotating tray that allows the X-ray Tech-
nician to change receptor orientation without removing the receptor from the
tray.
Detailed instructions for operation of the RT-DOK50-T is available in User and
Installation manual, Hoorn-Holland document number L05001L manual-01A.wpd
(shipped with the X-ray table).
CXDI-50G DIGITAL RECEPTOR CABINET OPTION (TYPES Q-DRT-CT AND
Q-DRT-CT-R)
Quantum offers rotating and non-rotating receptor tray models for Canon CXDI-
50G digital receptors used in QT-740 and QT-750 X-ray table applications. The
non-rotating version (Q-DRT-CT) provides a tray capable of receiving the
CXDI-50G receptor in portrait or landscape orientation (changed manually), while
the rotating version (Q-DRT-CT-R) provides a rotating tray that allows the X-ray
Technician to change receptor orientation without removing the receptor from the
tray.
Detailed instructions for operation of the Q-DRT-CT and Q-DRT-CT-R are available
in document DC30-093 (shipped with the X-ray table).

Chapter
4
USER
MAINTENANCE
4-1
4-2
Chapter 4 User Maintenance
OVERVIEW
This chapter is designed to assist the system user in maintaining the smooth opera-
tion of the table. The user is responsible for performing certain routine maintenance
and inspection procedures. Aside from routine maintenance, any abnormal noise,
vibration, or unusual performance should be investigated by a qualified service repre-
sentative. Preventive maintenance or any repair service should be performed only by
qualified service personnel.
WARNING! Failure to follow manufacturer’s or

service personnel’s recommendations may result
in serious injury.
USER MAINTENANCE
User maintenance consists of the following activities, which should be performed
on a daily basis:
• Visually inspect the table for wear and cleanliness
• Clean the tabletop, cassette tray, and exterior painted surfaces of the table
• Disinfect the table top surface after each use in accordancew with facility
requirements.
Cleaning
The system user is responsible for the basic cleanliness of the equipment. On
a regular basis, the table surface should be wiped clean. Painted metal sur-
faces should be cleaned using a clean cloth slightly moistened in warm soapy
water (use mild soap). Wipe with a clean wet cloth, then dry. Never use
abrasive polish on this equipment.
WARNING! Always disconnect the equipment

from the main power supply prior to any cleaning.
On 115 VAC systems, the power supply cord is the
power disconnect device. On 230 VAC systems,
the power disconnect is the main disconnect (or
power cable) on systems wired directly to facility
power.
To remove the cassette tray from the Receptor Cabinet for cleaning, proceed
as follows:
Midwest Trays
2. Pull the cassette tray out by the handle until it stops.
3. Grasp both sides of the tray with your right hand placed near the table
and your left hand towards the tray front.

Chapter 4 User Maintenance
4. Locate the spring-loaded lever on the right side of the tray bottom. A
spring-loaded plate covers this hole. Press the lever with your right index
finger, lift the cassette tray up slightly and pull the tray away from the
Receptor Cabinet.
Poersch Trays
2. Pull the cassette tray out by the handle until it stops.
3. Grasp the left side of the tray with your left hand.
4. Locate the square block at the back right side of the cassette tray. A
spring-loaded plate is on the front side of the block. While pressing the
plate, pull the tray out from the Receptor Cabinet.
CXDI-50G Digital Receptor CabinetOption (Type RT-DOK50-T)
Maintenance instructions for the Hoorn-Holland digital receptor tray (Quan-
tum option RT-DOK50-T) is described in detail in document User and Installa-
tion manual, Hoorn-Holland document number L05001L manual-01A.wpd
(shipped with the X-ray table).
Quantum Q-DRT-CT/Q-DRT-CT-R Trays for Canon CXDI-50G Digital
Receptors
Maintenance instructions for the Q-DRT-CT and Q-DRT-CT-R digital receptor
trays are described in detail in document DC30-093 (shipped with the X-ray
Table).

Chapter
5
WARRANTY
INFORMATION
5-1
5-2
Chapter 5 Warranty Information
WARRANTY STATEMENT
Quantum Medical Imaging, LLC (herein after known as “QMI”) warrants to the buyer
that any new product manufactured by QMI will be free from defects in material and
workmanship, and will substantially conform to the applicable specifications in effect
on the date of shipment when subjected to normal, proper and its intended use by
properly trained personnel. QMI shall be the sole judge in determining whether said
equipment or component is defective by reason of manufacture.
All QMI products shall be so warranted for a period of 12 months from the date of
original installation, such date to be evidenced by means of a completed Warranty
Card returned to QMI within 30 days of installation. In no case shall the warranty
extend beyond 15 months from the date of shipment. If the attached warranty card
is not so returned to QMI, then the warranty period will be deemed to have com-
menced on the date of shipment (the invoice date) and extend for a period of twelve
months. The buyer should submit only one such card per system or major compo-
nent purchased.
WARRANTY CARD

Clip or Copy Warranty Card on reverse side and submit to QMI
See Reverse Side for Warranty Card

WARRANTY STATEMENT (Continued)

Promptly complete the warranty card and mail or fax it to:
Quantum Medical Imaging, LLC
2002-B Orville Drive North
Ronkonkoma, N.Y. 11779 USA
631 567-5074 fax 631 567-5800 voice
Replacement components furnished by QMI to the Buyer/Dealer during the warranty
period shall be warranted for the remainder of the original product warranty or 90
days, whichever is longer. This warranty extends only to the original purchaser and is
not transferable unless expressly authorized in writing by Quantum Medical Imaging,
LLC.
Products manufactured by parties other than QMI, whereby QMI acts solely as distrib-
utor or reseller, are warranted exclusively by their manufacturers according to each of
their independent warranty terms and conditions.
Warranty consideration can only be given for defective QMI products properly
returned to the factory in accordance with the QMI Returned Materials Procedure
(refer to Dealer Price Book or contact QMI customer service).
WARRANTY EXCLUSIONS
The foregoing warranties are exclusive and in lieu of all other warranties, whether
written, oral, express, implied or statutory. NO IMPLIED WARRANTY OF MERCHANT-
ABILITY OR FITNESS FOR A PARTICULAR PURPOSE SHALL APPLY. Quantum Medical
Imaging, LLC Warranty is exclusive of:
1) Failure of the Buyer/Dealer to prepare the site and operating environment in
accordance with applicable instructions and recommendations of QMI.
2) Failure of Buyer/Dealer to provide the proper incoming power required to support
the equipment in accordance with the requirements of QMI.
3) Modification of QMI products performed by a party other than QMI.
4) Combining products deemed by QMI to be incompatible.
5) Improper or extraordinary use of a product, improper maintenance of the prod-
uct, or failure to comply with any applicable instructions and recommendations of
Quantum Medical Imaging, LLC.
6) Misuse, abuse, tampering, or negligent storage or handling of a product by the
Buyer, its employees, agents, or contractors.
7) Fuses, glassware, high voltage cables and other items deemed by QMI to be
expendable.
Acts of God, fires, floods, power failure or electrical power surges. Strikes, sabotage,
labor disturbances, war, riots, acts of civil or military authority, or other causes beyond
the reasonable control of QMI.
Installation, routine troubleshooting and repair are also excluded from warranty.
Technical service and maintenance is the responsibility of the Dealership selling the
equipment.

The Manufacturer is hereby relieved of all responsibility for damage during shipment
of the product following the freight carrier’s pick-up for transportation to the delivery
point.
BUYER’S REMEDIES
If QMI determines that a product fails to meet any specification during the applicable
warranty period, QMI shall correct any such failure as follows:
A) By repairing, adjusting, or replacing any defective or non-conforming component
or product.
B) By making available any necessary repair or replacement parts or assemblies for
exchange.
Quantum Medical Imaging, LLC shall have the option to furnish either new or rebuilt
replacement parts or assemblies for exchange. All returned parts shall become the
property of Quantum Medical Imaging, LLC upon exchange.
The preceding Paragraphs set forth the Buyer’s sole remedies and QMI’s sole liability
for claims based upon failure of the product to meet any warranty, whether the claim
is on contract, warranty, tort (including negligence and strict liability) or otherwise,
and however instituted.
Upon the expiration of the applicable warranty period, all such liability shall terminate.
In no event shall QMI be liable for special or consequential damages arising out of the
use of or inability to use its equipment, whatsoever.
The warranties and remedies available to the buyer are conditioned upon claims
under this warranty being made in accordance with the aforementioned warranty
statement.
WARRANTY RETURN PROCEDURE
A fully completed Field Returned Material Evaluation Form must be returned with any
defective product or any returned item. All returns must include the Serial Number of
the Equipment and the Specific Part Number written on the Field Returned Material
Evaluation Form. All freight charges resulting from Warranty Returns are the respon-
sibility of the Buyer/Dealer.
EQUIPMENT IN TRANSIT
QMI assumes no responsibility for equipment damaged in transit to or from QMI. To
protect the Buyer/Dealer, the receiver of any equipment should examine all cartons
and crates carefully at the time of delivery. If damage is apparent, make a notation
on the delivery receipt, request an inspection by the freight carrier, and if applicable,
file an appropriate carrier claim. Should concealed damage be detected, immediately
notify the carrier and request an inspection. The purchaser (Buyer/Dealer/Customer)
is fully responsible for the filing of freight damage claims to the freight carrier.
QMI assumes no responsibility for any loss or damage to products once they have
been shipped from our factory. As such, the Buyer/Dealer and Customer remain fully
responsible for payment to QMI for all invoices, according to our standard payment
terms, regardless of freight damage or processing of an insurance claim, by the
dealer or customer.

VOIDING WARRANTY
Tampering with, or any attempt at installation, maintenance, repair, service, reloca-
tion, or alteration of or to a QMI product, when performed by any person or entity
other than Quantum Medical Imaging, LLC or its Certified Dealer without the written
approval of an Authorized Person at Quantum Medical Imaging, LLC, shall immedi-
ately Void and Cancel all warranties with respect to the affected product.



DC30-006 Quantum QT-740 &amp; QT-750 Operator Manual Rev G

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DC30-006 Quantum QT-740 &amp; QT-750 Operator Manual Rev G

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Models QT-740 and QT-750

Manual Part No. DC30-006 Revision G

Copyright© 2009 QMI

Quantum Medical Imaging, LLC Made in U.S.A.

REVISION DATE TYPE OF MODIFICATION

B 3/14/01 Incorporated ECO 0245

C 5/17/01 Added UL mark

D 4/30/04 Incorporated ECO 1359

E 5/2/06 Incorporated ECO 1583

F 9/16/09 Incorporate ECO 2123, 2173, 2199, and updated

G 10/27/09 Incorporate ECO 2011, 2092

Page Page Page

1-1 thru 1-6 G

Models QT-740 & QT-750 - Operator’s Manual Revision G

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Revision G Models QT-740 & QT-750 - Operator’s Manual

Models QT-740 & QT-750 - Operator’s Manual Revision G

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Revision G Models QT-740 & QT-750 - Operator’s Manual

GENERAL SAFETY INFORMATION

WARNING Indicates injury or death is possible if the

NOTE Indicates essential information that should be

Models QT-740 & QT-750 - Operator’s Manual Revision G

in NCRP Reports available from NCRP Publications, 7910 Woodmont Ave-

MEDICAL ELECTRICAL EQUIPMENT

Revision G Models QT-740 & QT-750 - Operator’s Manual

Earth (ground) Type B Equipment

Protective Earth (ground) Attention, consult accompanying

Dangerous Voltage Enable tabletop float (releases

Enable Tabletop Up Motion Enable Tabletop Down Motion

Models QT-740 & QT-750 - Operator’s Manual Revision G

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Revision G Models QT-740 & QT-750 - Operator’s Manual

Models QT-740 & QT-750 - Operator’s Manual Revision G

Figure 2-1. Radiographic Table Main Components

Revision G Models QT-740 & QT-750 - Operator’s Manual

WARNING! To avoid damage to the table, any

WARNING! Do not allow patient to place his/her

TABLE TOP FLOAT MOTION (ALL MODELS)

WARNING! When transferring a patient on or off

Models QT-740 & QT-750 - Operator’s Manual Revision G

Figure 3-1. Patient Positioned on Table Top

FLOAT Foot Pedal

Figure 3-2. Model QT-740 FLOAT Foot Pedal Control

Revision G Models QT-740 & QT-750 - Operator’s Manual

FLOAT Foot Pedals

Figure 3-3. Model QT-750 - FLOAT Foot Pedal Controls

TABLE TOP FLOAT

MODEL QT-740 MODEL QT-750

Figure 3-4. Table Control Handle FLOAT Push Button Switch

Models QT-740 & QT-750 - Operator’s Manual Revision G

FOOT PEDAL/CONTROL HANDLE DISABLE SWITCH (ALL MODELS)

Figure 3-5. Foot Pedal/Control Handle Disable Switch Location

Revision G Models QT-740 & QT-750 - Operator’s Manual

ELEVATING MOTION (MODEL QT-750 ONLY)

Figure 3-6. Emergency Stop Switch Location

IMPORTANT! On Model QT-750 tables equipped

Models QT-740 & QT-750 - Operator’s Manual Revision G

DOWN PEDAL UP PEDAL

Figure 3-7. Model QT-750 - Up/Down Foot Pedal Controls

PRESS HERE TO ENABLE

PRESS HERE TO ENABLE

DC30-006 Quantum QT-740 & QT-750 Operator Manual Rev G

DC30-006 Quantum QT-740 & QT-750 Operator Manual Rev G