Quantum Q-Rad Operator’s Manual

Q-Rad System

Operator’s Manual

Manual Part No. DC30-091 Revision F

The original release of this manual dated 2011-02-24 (February 24, 2011) was drafted in the
English language by Quantum Medical Imaging, LLC.

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 © 2012 QMI

Quantum Medical Imaging, LLC
Division of Carestream

2002-B Orville Drive North
Ronkonkoma, NY 11779-7661 USA
Phone: [phone]
Fax: [phone]
E-mail: [email protected]
www.quantummedical.net

Made in U.S.A.

Revision History

Revision Date Type Of Modification

A 2011-02-24 Initial Release

B 2011-11-02 Added DX-D DR configuration

C 2011-08-30 Added QG-DIG-DRX integration option

D 2012-01-30 Incorporated ECO 2568, 2609

E 2012-02-10 Renamed Operator Manual, changed EU Representative

F 2012-05-09 Updated per IEC 60601-1: 2005, IEC 60601-1-3,

IEC 60601-2-54

Page

Number Rev

i thru iv F

1-1 thru 1-14 F

2-1 thru 2-18 F

Page

Number Rev

Page

Number Rev

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Revision History

REVISIO
N

A 2011-02-24--- Initial Release

B 2011-10-27All Various

DATE PAGES NOTES

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Table of Contents

Chapter 1: Safety Notices

General Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Warnings, Cautions, Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Regulatory Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5

Classification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-6

Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-6

Intended Operator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7

Training. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7

Applicable Standards. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7

Accompanying Documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7

Environmental Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-8

Electromagnetic Compatibility

(EN 60601-1-2:2007/IEC 60601-1-2:2007) . . . . . . . . . . . . . . . . . . . . . .1-8

Abbreviation Definition. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-13

Chapter 2: General Information

Instructions for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4

Component Weights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Generators (Cabinet) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Generators (Control Panel) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Tables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Tube Supports. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Upright Cassette Holders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Heat Dissipation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

Generators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

X-Ray Tube. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

Tables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

Tube Supports. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

Upright Cassette Holders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

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Table of Contents

System Operating Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

Transport and Non-Operating Environment. . . . . . . . . . . . . . . . . . . . . .2-7

System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8

Q-Rad Floor-Mounted System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8

Q-Rad “DRX Series” Integrated Radiography System . . . . . . . . . . . . . . .2-9

Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11

General Application Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11

Cleaning, Preventive Inspection and Maintenance . . . . . . . . . . . . . . . . . .2-11

Instructions for Disposal of Waste Equipment . . . . . . . . . . . . . . . . . . .2-11

Labeling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12

Power Disconnection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17

Detachable Parts and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-18

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Chapter

C

HAPTER

1: S

AFETY

N

1

OTICES

1-1

1-2

Chapter 1 Safety Notices

General Safety Information

This product has been designed to meet stringent safety standards. All medical
electrical equipment requires proper installation, operation, and maintenance
(particularly with regard to safety).

It is vital that the user read, understand, note, and where applicable, strictly observe
all Warnings, Cautions, Notes and Safety markings within this document and on the
equipment, and that the user strictly follow all safety directions in this manual to help
ensure the safety of users and patients.

Every reasonable precaution has been taken during manufacture to safeguard the
health and safety of persons who will operate this equipment. The following
precautions must be observed at all times.

Warnings, Cautions, Notes

The following samples show how warnings, cautions, and notes appear in this
document. The text explains their intended use.

Indicates injury or death is possible if the instructions

Warning

Caution

Note

The purpose of safety icons, such as those shown below, is to indicate at a glance the
type of caution, warning or danger.

Warning Ionizing radiation: indicates the possibility of

Warning Dangerous voltage: indicates the presence of high

Warning Warning, hot surface.

are not obeyed. Instructs users to refer to
documentation if displayed without warning text.

Indicates that damage to equipment is possible if the
instructions are not obeyed.

Notes provide advice and highlight unusual points. A
note is not intended as an instruction.

increased levels of radiation.

voltage.

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Chapter 1 Safety Notices

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 direc­tion 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. In the United States, Federal law restricts this
device to sale, distribution, and use by or on order of a licensed physician.

Quantum Medical Imaging, LLC cannot assume responsibility for any mal­functioning of this equipment resulting from improper operation, mainte­nance, or repair, or from damage or modification of its components.

Failure to observe these warnings may cause serious injuries.

WARNING

X-rays are hazardous to both patient and operator unless established safe
exposure factors and operating instructions are observed.

Only qualified and authorized personnel shall operate this system. In this
context, qualified means those legally permitted to operate this equipment
in the jurisdiction in which the equipment is being used, and authorized
means those authorized by the authority controlling the use of the equip­ment. Full use must be made of all radiation protection features, devices,
systems, procedures and accessories.

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
in NCRP Reports available from NCRP Publications, 7910 Woodmont Ave­nue, 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.

WARNING

X-ray equipment may cause injury if used improperly. The instructions con­tained 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.

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Chapter 1 Safety Notices

WARNING

Exterior surfaces of the X-ray Tube can rise in temperature to levels where
the operator or patient could suffer burns. Avoid contact with the tube
housing.

WARNING

Changes, additions or maintenance to the equipment carried out by per­sons without appropriate qualifications and training and/or using unap­proved spare parts may lead to serious risk of injury and damage to the
equipment as well as making the warranty void.

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
Diagnostic X-ray System” by the assembler (i.e., the installer) with the appropriate
agencies; 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
Quantum Medical Imaging, LLC.

Those responsible for the planning of x-ray equipment installations must be
thoroughly 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, participate in or supervise the operation of the equipment must be
thoroughly familiar and comply completely with the currently established safe
exposure factors and procedures described in publications such as Subchapter J of
Title 21 of the Code of Federal Regulations, “Diagnostic X-Ray Systems and Their
Major Components,” and NCRP Report No. 102, “Medical X-Ray, Electron Beam and
Gamma Ray Protection for Energies Up to 50 MeV—Equipment Design and Use” as
revised or replaced in the future.

This equipment must only be used in rooms that comply with all applicable laws or
regulations that have the force of law, concerning electrical safety for this type of
equipment.

Scheduled maintenance is essential to the assurance of continued integrity of this
equipment with respect to regulatory compliance. The continuance of certified
performance to the regulatory standard is incumbent upon the user's diligent
conformance to recommended maintenance instructions.

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Chapter 1 Safety Notices

N

Complies with EC Directive 93/42/EEC for Medical Devices,
FDA Center for Devices and Radiological Health (CDRH) - Title 21 CFR Subchapter J

EU Authorized Representative:

Carestream Health France
1, rue Galilée
93192 NOISY-LE-GRAND CEDEX
France

Classification

This product has been classified as Class I, Type B. This equipment is not suitable
for use in the presence of a flammable anesthetic mixture with air or with oxygen
or with nitrous oxide. Protection against Harmful Ingress of Water (Ordinary),
enclosed equipment without protection against ingress of liquids.

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

The following symbols may be used for marking on this equipment or equipment
documentation:

Non-ionizing Radiation Consult operating instructions

Earth (ground) Dangerous Voltage

Protective Earth (ground) Type B Equipment

Connection point for the
neutral conductor on
PERMANENTLY INSTALLED
EQUIPMENT

Alternating current

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Chapter 1 Safety Notices

Compatibility

The equipment described in this manual must only be used in combination with
other equipment or components if these are expressly recognized by Quantum
Medical Imaging, LLC as compatible.

Intended Operator

This equipment is intended to be installed, used and operated only in accordance
with the safety procedures given within this manual for the purpose for which it
was designed. Before attempting to work with this equipment, read, understand,
note and strictly observe all warnings, cautions and safety markings on the
equipment.

Users include those persons who actually handle the equipment and those who
have authority over the equipment.

Training

Users of this equipment shall have received adequate training on its safe and
effective use before attempting to work with the equipment. Training
requirements may vary from country to country. The User shall make sure that
training is received in accordance with local laws or regulations that have the
force of law.

Applicable Standards

The Q-Rad Radiographic System complies with:

• IEC 60601-1: 2005

• IEC 60601-1-2: 2007

• IEC 60601-1-3: 2008

• IEC 60601-1-6:2010

• IEC 62366: 2007

Accompanying Documentation

The documentation consists of a System Operator’s manual (this document),
System Service manual (DC30-109) and related documentation, depending on
system configuration, as shown in Chapter 2, GENERAL INFORMATION, Table
2-1. The documentation shall be kept with the system for easy reference.

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Chapter 1 Safety Notices

Environmental Protection

This equipment contains certain materials and chemical compounds incidental to the
manufacture of electrical and electronic equipment, and improper “end-of-life”
disposal of such equipment can result in environmental contamination. Therefore, this
equipment should not be disposed of as ordinary household waste, but should instead
be delivered to a designated electrical and electronic waste disposal or recycling
center. For further information on disposing of electrical and electronic waste, contact
the cognizant authority within the jurisdiction.

Electromagnetic Compatibility (EN 60601-1-2:2007/IEC 60601-1-2:2007)

The Q-Rad Radiographic System is intended for use in the electromagnetic
environment specified below. As such, Q-Rad Radiographic System must be installed
and put into service according to the information provided in the accompanying
Service Manual. Unauthorized changes to this product Do not make any modifications

Portable and mobile RF communications equipment can affect medical electrical
equipment. It is therefore recommended that the operation of equipment of this type
such as mobile telephones, cordless microphones and other similar mobile radio
equipment be restricted from the vicinity of this device.

Use of accessories, transducers and cables other than those specified in the
accompanying documents, may result in increased emissions or decreased immunity
of the equipment.

Guidance and manufacturer's declaration - electromagnetic emissions

The Q-Rad Radiographic System is intended for use in the electromagnetic environment spec­ified below. The customer or the user of the Q-Rad Radiographic System should assure that it
is used in such an environment.

Emissions test Compliance Electromagnetic environment -

guidance

RF emissions
CISPR 11

Group 1 The Q-Rad Radiographic System

uses RF energy only for their internal
functions. Therefore, the RF emis­sions are very low and are not likely
to cause any interference in nearby
electronic equipment.

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Chapter 1 Safety Notices

Guidance and manufacturer's declaration - electromagnetic emissions

RF emissions
CISPR 11

Harmonic emissions
IEC 61000-3-2

Voltage fluctuations/
flicker emissions
IEC 61000-3-3

Class A The Q-Rad Radiographic System is

suitable for use in all establishments

Class A

Complies

other than domestic and those
directly connected to the public low­voltage power supply network that
supplies buildings used for domestic
purposes.

Guidance and manufacturer's declaration - electromagnetic immunity

The Q-Rad Radiographic System is intended for use in the electromagnetic environment specified below. The
customer or the user of the Q-Rad Radiographic System should assure that it is used in such an environment.

Immunity test IEC 60601

test level

Electrostatic
discharge (ESD)
IEC 61000-4-2

±6 kV contact
±8 kV air

Compliance

level

±6 kV contact
±8 kV air

Electromagnetic environment

- guidance

Floors should be wood, con­crete or ceramic tile. If floors are
covered with synthetic material,
the relative humidity should be
at least 30 %.

Electrical fast
transient/burst
IEC 61000-4-4

Surge
IEC 61000-4-5

±2 kV for power supply
lines
±1 kV for input/output
lines

±1 kV differential mode
±2 kV common mode

±2 kV for power supply
lines
±1 kV for input/output
lines

±1 kV differential mode
±2 kV common mode

Mains power quality should be
that of a typical commercial or
hospital environment.

Mains power quality should be
that of a typical commercial or
hospital environment.

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Chapter 1 Safety Notices

Guidance and manufacturer's declaration - electromagnetic immunity

Voltage dips,
short interruption,
and voltage
variations on power
supply
input lines
IEC 60601-4-11

Power frequency
(50/60 Hz)
IEC 61000-4-8

NOTE: U

is the A.C. mains voltage prior to application of the test level.

T

< 5 % U

T

(>95 % dip in UT)
for 0.5 cycle

< 5 % U

T

(>95 % dip in UT)
for 0.5 cycle

Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the Q-Rad Radiographic Sys-

40 % U

T

(60 % dip in UT)
for 5 cycles

70 % U

T

(30 % dip in UT)
< 5 % U

T

(> 95 % dip in UT)
for 5 s

40 % U

T

(60 % dip in UT)
for 5 cycles

70 % U

T

(30 % dip in UT)
< 5 % U

T

(> 95 % dip in UT)
for 5 s

tem requires continued opera­tion during power mains
interruptions, it is recommended
that the Q-Rad Radiographic
System be powered from an
uninterruptible power supply or
battery.

3 A/m 3 A/m Power frequency magnetic

fields should be at levels char­acteristic of a typical location in
a typical commercial or hospital
environment

Guidance and manufacturer's declaration - electromagnetic immunity

The Q-Rad Radiographic System is intended for use in the electromagnetic environment specified
below. The customer or the user of the Q-Rad Radiographic System Q-Rad Radiographic System
should assure that it is used in such an environment.

Immunity test IEC 60601

test level

Compliance

level

Electromagnetic environment -

guidance

Portable and mobile RF communications
equipment should be used no closer to any
part of the Q-Rad Radiographic System,
including cables, than the recommended
separation distance calculated from the
equation applicable to the frequency of the
transmitter.

Recommended separation distance

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Chapter 1 Safety Notices

Pd 2,1

Pd 2,1

Pd 3,2

Guidance and manufacturer's declaration - electromagnetic immunity

Conducted RF
IEC 61000-4-6

Radiated RF
IEC 61000-4-3

3 Vrms
150 kHz to 80
MHz

3 V/m
80 MHz to 2,5
GHz

3 Vrms

3 V/m

, 80 MHz to 800 MHz

, 800 MHz to 2,5 GHz

where P is the maximum output power rat­ing of the transmitter in watts (W) accord­ing to the transmitter manufacturer and d
is the recommended separation distance in
metres (m).

Field strengths from fixed RF transmitters,
as determined by an electromagnetic site

a

survey

ance level in each frequency range.
Interference may occur in the vicinity of
equipment marked with the following sym­bol:

, should be less than the compli-

b

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.

a

Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) tele­phones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot
be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF
transmitters, an electromagnetic site survey should be considered. If the measured field strength in
the location in which the Q-Rad Radiographic System is used exceeds the applicable RF compliance
level above, the Q-Rad Radiographic System should be observed to verify normal operation. If abnor­mal performance is observed, additional measures may be necessary, such as re-orienting or relocat­ing the Q-Rad Radiographic System.

b

Over the frequency range 150 kHz to 80 kHz, field strengths should be less than 3 V/m.

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Chapter 1 Safety Notices

Pd 2,1

Pd 2,1

Pd 3,2

Recommended separation distances between

portable and mobile RF communications equipment and the

Q-Rad Radiographic System

The Q-Rad Radiographic System is intended for use in an electromagnetic environment in which radi­ated RF disturbances are controlled. The customer or the user of the Q-Rad Radiographic System Q­Rad Radiographic System can help prevent electromagnetic interference by maintaining a minimum dis­tance between portable and mobile RF communications equipment (transmitters) and the Q-Rad Radio­graphic System as recommended below, according to the maximum output power of the communications
equipment.

Rated maximum output power

of transmitter

W

0,01 0,12 0,12 0,23

0,1 0,38 0,38 0,73

1 1,2 1,2 2,3

10 3,8 3,8 7,3

100 12 12 23

For transmitters rated at a maximum output power not listed above, the recommended separation dis­tance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter,
where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.

NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.

Separation distance according to frequency of transmitter

m

150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz

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Chapter 1 Safety Notices

Abbreviation Definition

The following abbreviations and acronyms may be found in this document. Their
definition is explained below.

AEC Automatic Exposure Control

Btu British Thermal Unit

CR Computed Radiography

dDistance

DR Digital Radiography

HF High Frequency

hPa Hecto-Pascal

hr Hour

kg Kilogram

kHz Kilohertz

KVA Kilovolt-Ampere

lb Pound

m Meter

MHz Megahertz

mm Millimeter

OCP Operator Control Panel

P Power (max.)

RF Radio Frequency

VVolt

WWatt

WEEE Waste Electrical and Electronic Equipment

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Chapter

C

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ENERAL

I

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2

2-1

2-2

Chapter 2 General Information

Instructions for Use

The instructions for using Quantum’s Q-Rad Radiographic System, including an explanation of the function
of controls, displays and signals, and the sequence of operation, are contained in each of the system
component user’s manual indicated in Tabl e 2- 1.

WARNING: This equipment must be operated with reasonable care.
Manufacturer’s equipment recommendations described in this manual mus t
be observed.

WARNING: Use a focal spot-to-film distance as large as possible in order to
keep the absorbed dose to the patient as low as reasonably achievable.

WARNING: During each exposure, the individual operating the X-ray
machine must exit the radiographic operatory and stand behind a leaded
wall.

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Chapter 2 General Information

Overview

This chapter describes the configurations of the Q-Rad Radiographic System, which typically includes
Quantum Medical Imaging HF Series X-ray Generators, radiographic tables, free-standing tube support,
upright cassette holder, collimator, X-ray tube, ion chamber (when equipped with AEC option), and image
receptor.

Detailed instructions for successful integration of the compatible Quantum components are published in
the Service Manuals for each of the various system components.

Table 2-1. Q-Rad System Components User/Service Documents

Component Type Model(s) User Manual P/N Service Manual

P/N

X-ray Generator,
Single-phase, non­Stored Energy

X-ray Generator,
Single-phase, Stored
Energy

X-ray Generator,
Three-phase

TechVision Supple­mentary Generator
Control Panel

Radiographic Table,
Elevating Tabletop

Radiographic Table,
Non-Elevating Table­top

QG-25, QG-25-5,
QG-32, QG-32-5,
QG-40, and QG-40-5

QG-20-SE, QG-32-SE,
QG-40-SE, QG-50-SE

QG-32-2, QG-32-3,
QG-40-2, QG-40-3,
QG-50, QG-50-2,
QG-65, and QG-80

QG-TV-Q, QG-TV-IP-Q,
QG-TV-F, QG-TV-IP-F, QG­TV-C, QG-TV-IP-C

QT-750 DC30-006 DC30-007

QT-740 DC30-006 DC30-007

Odyssey - DC30-010
Quest - DC30-015
Q-Vision - DC30-101

Odyssey - DC30-010
Quest - DC30-015
Q-Vision - DC30-101

Odyssey - DC30-010
Quest - DC30-015
Q-Vision - DC30-101

DC30-048 (Quantum
non-integrated systems,
DC30-120 (Q-Vision
non-integrated sys­tems)
DC30-126 (Carestream
integrated systems)

Q-Vision/Odyssey ­DC30-011
Quest - DC30-063

Q-Vision/Odyssey ­DC30-011
Quest - DC30-063

Q-Vision/Odyssey ­DC30-011
Quest - DC30-063

DC30-049

Radiographic Table,
Non-Elevating Table­top

Tube Support, Floor/
Wall Mounted

Tube Support, Free­Standing (Floor)
Mounted

QT-730 DC30-003 DC30-003

QS-500 DC30-034 DC30-005

QS-550 DC30-034 DC30-009

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Chapter 2 General Information

Table 2-1. Q-Rad System Components User/Service Documents

Component Type Model(s) User Manual P/N Service Manual

P/N

Radiographic Upright
Cassette Holder,

Collimator, Manual Progeny, MC150

Collimator, Automatic Progeny, Linear II

Collimator, Program­mable

X-ray tube Toshiba E7239X, E7242X,

DX-D 500

Digital DRX Series
Integration Software
(QG-DIG-DRX)
(Optional)

n

Q-Rad

QW-420, QW-420-S, QW­420-D, QW-400

Huestis, 150MC
Ralco R108

Progeny, Linear IV

Huestis, CM-32211-QMI CM-21-002 CM-21-002

E7252X, E7254X, E7869X

Varian RAD-14, RAD-60,
RAD-92

Dunlee DA 1092, DA 1036

QG-DIG-DRX DC30-123 DC30-123

DC30-039 DC30-040

00-02-1078
CM-21-001
MTR108

00-02-1559
00-02-1517

Refer to data sheet pro­vided with tube

00-02-1078
CM-21-001
MTR108

00-02-1559
00-02-1517

Refer to data sheet
provided with tube

Dose Area Product
(DAP) meter
(Optional)

Vacutec VacuDAP OEM DAP-std-fl-

tw_BA011.3.doc

DAP-std-fl­tw_BA011.3.doc

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Chapter 2 General Information

Component Weights

Generators (Cabinet)

Single-Phase,
non-Stored Energy (SE) units: 135.2 kg (298.0 lb)

32, 40, and 50 kW,
SE units: 195.5 kg (431.0 lb)

Three-Phase units: 172.4 kg (380.0 lb)

Generators (Control Panel)

Odyssey (without pedestal): 2.3 kg (5.0 lb)
Odyssey (with pedestal): 11.3 kg (25.0 lb)
Quest (without pedestal): 1.8 kg (4.0 lb)
Quest (with pedestal): 10.9 kg (24.0 lb)
Q-Vision: 5.9 kg (13.0 lb)
TechVision Option: 4.3 kg (9.5 lb)

without internal High Speed Starter (HSS)

176.0 kg (388.0 lb)
with internal High Speed Starter (HSS)

Tables

Model QT-730: 79.4 kg (175.0 lb)
Model QT-740: 158.8 kg (350.0 lb)
Model QT-750: 226.8 kg (500.0 lb)

Tube Supports

Model QS-550: 272.2 kg (600.0 lb)
Model QS-500: 230.4 kg (508.0 lb)

Upright Cassette Holders

Model QW-420: 102.1 kg (225.0 lb)
Model QW-420-S: 102.1 kg (225.0 lb)
Model QW-420-D: 90.7 kg (200.0 lb)
Model QW-400: 45.4 kg (100.0 lb)

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Heat Dissipation

Generators

Cabinet Typical Heat Output: 3600 BTU per hour
Control Panel Typical Heat Output: 130 BTU per hour

X-Ray Tube

Max. Heat Output (600 khu tube): 2000 BTU per hour

Tables

QT-730 Typical Heat Output: 40 BTU per hour (from receptor)
QT-750 Typical Heat Output: 400 BTU per hour
QT-740 Typical Heat Output: 100 BTU per hour

Tube Supports

QS-500/QS-550: 200 BTU per hour

Upright Cassette Holders

Typical Heat Output: 50 BTU per hour

Chapter 2 General Information

NOTE: The above calculations are typical, based upon average usage. Air

circulation around the electronic cabinets must be provided. This
includes the sides, back, front, and top of cabinet.

System Operating Environment

Ambient Temperature: 10–40 °C (50–104 °F)
Relative Humidity: 15–75 %
Atmospheric Pressure: 700–1060 hPa

Transport and Non-Operating Environment

Ambient Temperature: -25 to +55 °C (-13 to 131 °F)
Relative Humidity: 5–95 %
Atmospheric Pressure: 500–1060 hPa

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Chapter 2 General Information

System Configuration

The Quantum Q-Rad System consists of a combination of integrated radiographic components, typically
including an X-ray generator, X-ray tube and tube support, collimator, radiographic table, and an upright
cassette holder. Different types of image receptors may be utilized with the Q-Rad System, including
computed radiography (CR) receptors, as well as conventional analog film cassettes.

Q-Rad Floor-Mounted System

The Q-Rad Floor-Mounted system is configured around either a free-standing,
floor-mounted tube support (Model QS-550) or a wall/ceiling mounted tube support (Model QS-500).
Because the free-standing version does not require wall attachment for support, it provides enhanced
freedom of movement in the patient vicinity for the operator.

Recumbent examinations are accomplished utilizing an elevating (Model QT-750) or the
non-elevating (Model QT-740 and QT-730) radiologic tables. Standing (weight-bearing) examinations
are performed using an upright, non-tilting (Model QW-420 Series) chest stand (cassette holder).

The X-ray generator is available in various power output and operator control panel types, with the
typical configuration including a 80 kW output generator with an Odyssey operator control.

Table 2-2. Q-Rad Floor Mounted System

COMPONENT COMPONENT

COMPONENT MODEL#

DESIGNATION

GENERATOR QG1 SINGLE-PHASE: QG-25-1, QG-32-1, QG-40-1

STORED ENERGY
QG-40-SE, QG-50-SE
THREE-PHASE
QG-40-3, QG-50-3, QG-65-3, QG-80-3

GENERATOR
CONTROL PANEL

SUPPLEMENTAL
GENERATOR
CONTROL PANEL
(TECHVISION)

TABLE QT1 QT-730, QT-740, QT-750

TUBE SUPPORT QS1 QS-500, QS-550

WALL STAND QW1 QW-420, QW-420-D, QW-420-S, QW-400

OCP1 QUEST SERIES

QG-400, QG-500
ODYSSEY SERIES
QG-5000, QG-6500, QG-8000
Q-VISION SERIES
QGV-65, QGV-80

OCP2 QG-TV-IP-F

: QG-20-SE, QG-32-SE,

: QG-32-2, QG-32-3, QG-40-2,

: QG-200, QG-250, QG-320,

: QG-3200, QG-4000,

: QGV-32, QGV-40, QGV-50,

X-RAY TUBE TU1 TOSHIBA

E7869X
VARI A N
DUNLEE

: E7239X, E7242X, E7252X, E7254X,

: RAD-14, RAD-60, RAD-92

: DA 1092, DA 1036

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Table 2-2. Q-Rad Floor Mounted System

COMPONENT COMPONENT

COMPONENT MODEL#

DESIGNATION

COLLIMATOR QC1 PROGENY

LINEAR II, LINEAR IV
RALCO
HUESTIS

DAP QD1 VacuDAP-OEM DISPLAY + ION CHAMBER,

VacuDAP ION CHAMBER

ION CHAMBER IN1 AID

IMAGE
RECEPTOR

RC1 GRID CABINET

: ICX 1153

BUCKY CABINET
KLB10-08013

: MC150, MC150 PINNACLE,

: R 108/464 DHHS

: 150MC (MANUAL), CM 32211-QM1

: R50-17GC

: PROGENY KLB10-08011,

Q-Rad “DRX Series” Integrated Radiography System

The Q-Rad DRX Series Integrated Digital Radiography (DR) System combines the Q-Rad System’s HF
Series X-ray Generator and Carestream DRX-1 Digital Imaging Systems by way of a common user
interface (QG-DIG-DRX Software) running on the Carestream DRX-1 Digital Imaging System’s
Workstation computer.

When QG-DIG-DRX Software is implemented, all user interaction (except PREP and EXPOSE) with the
HF Series X-ray Generator is accomplished via the Digital Imaging System’s touchscreen computer,
thereby eliminating the need for a separate generator Operator Control Panel.

The Q-Rad DRX Series Integrated System consists of either a fixed DR Detector, and/or a Portable DR
Detector, and a Workstation Computer. The DR System is connected to the Quantum X-Ray Generator
by way of a software interface module.

Table 2-3. Q-Rad System, DRX Series Integration

COMPONENT COMPONENT

DESIGNATION

GENERATOR QG1 SINGLE-PHASE

STORED ENERGY
QG-40-SE, QG-50-SE
THREE-PHASE
QG-40-3, QG-50-3, QG-65-3, QG-80-3

GENERATOR CON­TROL PANEL

SUPPLEMENTAL
GENERATOR CON­TROL PANEL (TECH­VISION)

TABLE QT1 QT-730, QT-740, QT-750

OCP1 Q-CONNECT (WITH DRX-1 WORKSTATION)

QG-DIG-DRX

OCP2 QG-TV-IP-C, QG-TV-IP-F

COMPONENT MODEL#

: QG-32-1, QG-40-1

: QG-32-SE,

: QG-32-2, QG-32-3, QG-40-2,

:

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Chapter 2 General Information

Table 2-3. Q-Rad System, DRX Series Integration

COMPONENT COMPONENT

DESIGNATION

TUBE SUPPORT QS1 FLOOR-MOUNTED: QS-500, QS-550

WALL STAND QW1 QW-420, QW-420-D, QW-420-S

X-RAY TUBE TU1 TOSHIBA

E7869X
VARIAN
DUNLEE

COLLIMATOR QC1 PROGENY

LINEAR II, LINEAR IV
RALCO
HUESTIS
(PROGRAMMABLE)

DAP QD1 VacuDAP-OEM DISPLAY + ION CHAMBER,

VacuDAP ION CHAMBER

ION CHAMBER IN1 AID

IMAGE
DETECTOR CABINET

RC1 FIXED DETECTOR

: ICX 1153

Q-FDR-T (TABLE)
PORTABLE DETECTOR
STAND), Q-DRT-T (TABLE)

COMPONENT MODEL#

: E7239X, E7242X, E7252X, E7254X,

: RAD-14, RAD-60, RAD-92

: DA 1092, DA 1036

: MC150, MC150 PINNACLE,

: R 108/464 DHHS

: 150MC (MANUAL), CM-32211-QMI

: Q-FDR (WALL STAND),

: Q-DRT (WALL

DR IMAGING DETEC­TOR/SYSTEM

QR1, QR2 CARESTREAM DRX-1 IMAGING SYSTEM

(PORTABLE, WIRELESS)
CARESTREAM DRX-1 IMAGING SYSTEM
(FIXED, 4343R)

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Chapter 2 General Information

Intended Use

The Quantum Q-Rad System provides diagnostic quality images to aid the physician with diagnosis. The
system can be used to perform radiographic exposures of the skeleton (including skull, spinal column, and
extremities), chest, abdomen, and other body parts. The Q-Rad Radiographic System is not indicated for
use in mammography.

General Application Specification

Patient Population:

Age: Newborn to geriatric
Weight: Up to 294.8 kg (650.0 lb)
Region of Body: Produces images of any bone in the human body,

including the hand, wrist, arm, foot, ankle, knee, leg, or
spine.

Operator Requirements:

Education/Training: This equipment is sold to be used exclusively under the

prescribed direction of a person who is licensed by law
to operate equipment of this nature.

Application:

Location: Professional use only, indoor use only.
Physical Environment: Refer to Q-Rad System operating and non-operating

specifications in this chapter.

Frequency of Use: Intermittent operation, limited primarily by loading

characteristics specific to tube type used in the system.

Mobility: Stationary

Cleaning, Preventive Inspection and Maintenance

Instructions for cleaning, preventive inspection and routine maintenance of Q-Rad Radiographic System,
are included in each of the system component user’s and service manuals indicated in Table 2- 1 .

Instructions for Disposal of Waste Equipment

In the European Union, this symbol indicates that when the last user wishes to
discard this product, it must be sent to appropriate facilities for recovery and
recycling. Contact your local representative for additional information on the
collection and recovery programs available for this product.

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Chapter 2 General Information

REGULATORY

LABEL

CONFIGURATION

LABEL

GENERATOR CABINET

GENERATOR
COMPLIANCE
LABEL

Labeling

Each component of the Q-Rad System has its own rating plate/serial label. The following table provides the
general location of the rating plate/serial label on each of the various types of components that could be
incorporated in a Q-Rad System.

Table 2-4. Q-Rad System Components Labeling Guide

Component Type Model(s) Label Location

Q-Rad System Q-Rad

X-ray Generator Single-phase,

non-Stored Energy
QG-25, QG-25-5,
QG-32, QG-32-5,
QG-40, and QG-40-5

Single-phase, Stored
Energy
QG-20-SE, QG-32-SE,
QG-40-SE, QG-50-SE

Three-phase
QG-32-2, QG-32-3,
QG-40-2, QG-40-3,
QG-50, QG-50-2,
QG-65, and QG-80

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Chapter 2 General Information

compliance label

Table 2-4. Q-Rad System Components Labeling Guide

Component Type Model(s) Label Location

TechVision

Supplementary Gener-

ator Control Panel

Radiographic Table Fixed Non-Float Tabletop

Radiographic Table Non-Elevating Tabletop

QG-TV-F,
QG-TV-IP-F,
QG-TV-C,
QG-TV-IP-C

QT-730

QT-740

Elevating Tabletop
QT-750

Tube Support,

Floor Mounted

QS-500
QS-550

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Chapter 2 General Information

Table 2-4. Q-Rad System Components Labeling Guide

Component Type Model(s) Label Location

Radiographic Upright
Cassette Holder

Collimator, Manual PROGENY MC-150

QW-420,
QW-420-S, QW-420-D
QW-400

HUESTIS 150MC
RALCO R108/484 DHHS

Collimator, Automatic PROGENY Linear II,

Linear IV
HUESTIS CM-32211-QM1

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Chapter 2 General Information

X-RAY TUBE

COMPLIANCE LABEL

LOCATIONS

REAR VIEW

COMPLIANCE

LABEL/DATAPLATE

CABINET (FRONT)

Table 2-4. Q-Rad System Components Labeling Guide

Component Type Model(s) Label Location

X-ray tube

VARI A N:

RAD-14, RAD-60,
RAD-92

TOSHIBA:

DUNLEE:

Digital Image Detector

Cabinet

E7239X, E7242X,
E7252X, E7254X,
E7869X

DA 1092, DA 1036

Q-DRT
Q-DRT-T
Q-FDR
Q-FDR-T

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Chapter 2 General Information

REAR VIEW

COMPLIANCE

LABEL

Table 2-4. Q-Rad System Components Labeling Guide

Component Type Model(s) Label Location

Integration Option Q-Rad DRX Series

(QG-DIG-DRX)

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Chapter 2 General Information

Power Disconnection

Refer to the following table for Q-Rad System component power disconnection methods.

Table 2-5. DX-D 500

n

Q-Rad System Component Power Disconnection Method

Component Type Model Means of Power

Disconnect

X-ray Generator,
Single-phase, non­Stored Energy

X-ray Generator,
Single-phase, Stored
Energy

X-ray Generator, Three­phase

TechVision Supplemen­tary Generator Control
Panel

Radiographic Table,
Non-Elevating Tabletop

Radiographic Table,
Non-Elevating Tabletop

QG-25, QG-25-5,
QG-32, QG-32-5,
QG-40, and QG-40-5

QG-20-SE, QG-32-SE,
QG-40-SE, QG-50-SE

QG-32-2, QG-32-3,
QG-40-2, QG-40-3,
QG-50, QG-50-2,
QG-65, and QG-80

QG-TV-Q, QG-TV-IP-Q,
QG-TV-F, QG-TV-IP-F,
QG-TV-C, QG-TV-IP-C

QT-730 ON/OFF circuit breaker

QT-740 Unplug Line Cord

ON/OFF circuit breaker
CB1 on generator cabinet

ON/OFF circuit breaker
CB1 on generator cabinet

ON/OFF circuit breaker
CB1 on generator cabinet

ON/OFF circuit breaker
CB1 on generator cabinet

CB1 on generator cabinet

Radiographic Table,
Elevating Tabletop

Tube Support, Floor/Wall
Mounted

Tube Support, Free­Standing (Floor)
Mounted

QT-750 Unplug Line Cord

QS-500 ON/OFF circuit breaker

CB1 on generator cabinet

QS-550 ON/OFF circuit breaker

CB1 on generator cabinet

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Chapter 2 General Information

Table 2-5. DX-D 500

n

Q-Rad System Component Power Disconnection Method

Component Type Model Means of Power

Disconnect

Radiographic Upright
Cassette Holder, Non­Tilting

Collimator, Manual Progeny, MC150

Collimator, Automatic Progeny, Linear II

X-ray tube Toshiba E7239X, E7242X,

Dose Area Product
Meter (optional)

QW-420, QW-420-S,
QW-420-D, QW-400

Huestis, 150MC
Ralco, R108

Progeny, Linear IV
Huestis Programmable,
CM-32211-QMI

E7252X, E7254X, E7869X
Varian RAD-14, RAD-60,
RAD-92
Dunlee DA 1092, DA1036

Vacutec Display Unit:
VacuDAP OEM (QD1-2)
Vacutec Ion Chamber: Vac­uDAP OEM (QD1-1)

ON/OFF circuit breaker
CB1 on generator cabinet

ON/OFF circuit breaker
CB1 on generator cabinet

Unplug Line Cord (ACS
Power Supply & Junction
Box)

ON/OFF circuit breaker
CB1 on generator cabinet

Unplug Line Cord

Carestream Digital
Imaging System

DRX-1 Quick Reference Card for

the Carestream DRX-1
System, document 8G8318
Carestream DRX-1 System
Safety and Regulatory
Information with Hardware
User’s Guide, document
7H8166
Carestream DRX-1 System
Battery Charger User’s
Guide, document 8H6193

Detachable Parts and Accessories

Instructions for detachable parts and accessories of Q-Rad Radiographic System are included in each of
the system component user’s manual indicated in Tab le 2 -1 .

<End of Document>

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