Quantum Q DRT Manual
Quantum Q DRT Manual
Quantum Q DRT Manual
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)
SAFETY NOTICES
GENERAL SAFETY INFORMATION ............................................................ v
WARNINGS, CAUTIONS, NOTES............................................................... v
REGULATORY COMPLIANCE ...................................................................vii
COMPATIBILITY ..............................................................................vii
INTENDED OPERATOR .....................................................................vii
TRAINING ...................................................................................... viii
ACCOMPANYING DOCUMENTATION ................................................. viii
ENVIRONMENTAL PROTECTION ............................................................ viii
ABBREVIATION DEFINITION .................................................................. ix
WARRANTY INFORMATION
WARRANTY STATEMENT ........................................................................ xi
WARRANTY STATEMENT (Continued) ..................................................... xiii
WARRANTY EXCLUSIONS ...................................................................... xiii
BUYER’S REMEDIES ..............................................................................xiv
WARRANTY RETURN PROCEDURE .........................................................xiv
EQUIPMENT IN TRANSIT .......................................................................xiv
VOIDING WARRANTY..............................................................................xv
CHAPTER 1 - INTRODUCTION
OVERVIEW .......................................................................................... 1-3
KEY FEATURES .............................................................................. 1-3
Intended Use ................................................................................. 1-3
MAIN COMPONENTS ............................................................................ 1-4
Q-DRT DETECTOR TRAY CHARACTERISTICS ......................................... 1-5
CHAPTER 2 - SPECIFICATIONS
PRODUCT SPECIFICATIONS ................................................................. 2-3
General Specifications .................................................................... 2-3
Design .................................................................................... 2-3
Physical Characteristics .................................................................. 2-3
ENVIRONMENTAL SPECIFICATIONS ................................................ 2-4
System Operating Environment ................................................. 2-4
Non-Operating Environment ..................................................... 2-4
COMPATIBILITY STATEMENT ............................................................... 2-4
CHAPTER 4 - OPERATION
OPERATION OF Q-DRT ROTATING TRAYS ............................................ 4-3
OPERATION OF Q-DRT ROTATING TRAYS MOUNTED TO
VERTICAL WALL STANDS ............................................................... 4-3
Q-DRT ROTATING PORTABLE DETECTOR
TRAY OPERATION ................................................................... 4-3
OPERATION OF Q-DRT ROTATING TRAYS MOUNTED TO
RADIOGRAPHIC TABLES ................................................................. 4-6
IMAGING IN PORTRAIT ORIENTATION ..................................... 4-6
CHANGING DETECTOR ORIENTATION TO LANDSCAPE ............... 4-8
OPTIONAL REMOVABLE GRID OPERATION ...................................... 4-9
CHAPTER 5 - MAINTENANCE
OVERVIEW .......................................................................................... 5-3
USER MAINTENANCE ..................................................................... 5-3
PLANNED MAINTENANCE ............................................................... 5-3
REPLACEMENT PARTS AND ORDERING INFORMATION .................... 5-3
ORDERING INFORMATION ............................................................. 5-4
Removal and Replacement Procedure for Phenolic Panel
(Wall Stands Only) ................................................................... 5-7
Removal and Replacement of Detent Bumpers
(Rotary Models Only) ............................................................... 5-8
Removal and Replacement of the Sliding Tray Latch
(Rotary Models Only) ............................................................... 5-9
Removal and Replacement of the Chin Rest
(Wall Stands Only .................................................................. 5-10
Removal and Replacement of Push/Pull Catch .......................... 5-12
Removal and Replacement of Receptor Lock Micro Switch
(Table Models Only) ............................................................... 5-13
The purpose of safety icons, such as those shown below, is to indicate at a glance the
type of caution, warning or danger.
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 mal-
functioning of this equipment resulting from improper operation, mainte-
nance, 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 equip-
ment. 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 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, man-
ufactured, and calibrated to comply with governing Federal Regulations 21 CFR Sub-
chapter 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 Quantum
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.
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 perfor-
mance to the regulatory standard is incumbent upon the user's diligent conformance
to recommended maintenance instructions.
The following symbols may be used for marking on this equipment and/or equipment
documentation:
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 equip-
ment.
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 require-
ments 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.
ACCOMPANYING DOCUMENTATION
The documentation consists of an Installation & Operation manual (this docu-
ment) and related documentation:
• Service Manual P/N DC30-007: Contains technical and service documentation
for radiographic tables, into which this product may be installed
• Service Manual P/N DC30-040: Contains technical and service documentation
for casette holders, into which this product may be installed
The documentation shall be kept with the system for easy reference.
ENVIRONMENTAL PROTECTION
This equipment may contain 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 cen-
ter. For further information on disposing of electrical and electronic waste, contact the
cognizant authority within the jurisdiction.
ABBREVIATION DEFINITION
The following abbreviations and acronyms may be found in this document. Their def-
inition is explained below.
DR Digital Receptor
hPa Hectopascal
kg Kilograms
mm Millimeters
in. Inch(es)
lb Pound(s)
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 commenced
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 component pur-
chased.
WARRANTY CARD
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.
INTRODUCTION
1-1
1-2
Chapter 1 Introduction
OVERVIEW
This document is intended to assist users in the safe and effective operation of the
equipment described herein. Pay special attention to all the information described in
the Safety section (refer to SAFETY NOTICES).
This manual is written for trained users of the Q-DRT Series rotating X-ray image
detector trays for portable digital detector panels, hereinafter referred to as the Q-
DRT Trays, and for authorized field service personnel. Quantum Medical Imaging, LLC
assumes no liability for use of this document if any unauthorized changes to the con-
tent or format have been made.
KEY FEATURES
It is imperative that all safety procedures described in this manual be strictly
adhered to, in order to ensure the safety of both patient and user. The significant
physical and performance characteristics of the Q-DRT Trays are as follows:
• Q-DRT models to accommodate popular portable 14" x 17" Digital
Receptor (DR) panels, including, Agfa/Varian 4336, Carestream DRX-1
portable wireless, Vatech (Samsung) Xmaru 1417, and Thales 3543.
• All Q-DRT Trays feature a convenient drawer slide for easy installation
and removal of portable detector panel.
• Q-DRT models are compatible with Quantum’s Model QT-740 & QT-750
Radiographic Tables, and QW-420 Wall Stands where 14" x 17" portable
image detectors are used.
• Various options are available for left or right side loading trays on
Quantum QW-420 vertical wall stands, and fixed or elevating, float-top
QT-740 and QT-750 radiographic tables, including rotation of the
cassette holder to accommodate either portrait or landscape exposures.
• Removable grid and ion chamber options are available.
This product is intended to be used and operated only in accordance with the
safety procedures given within this manual for the purpose for which it was
designed. The intended use is given below. Nothing stated in this manual reduces
user's professional responsibilities for sound judgment and best practice.
INTENDED USE
Model Q-DRT Trays are intended for integration with new or existing Quantum
radiographic tables and wallstands, and are to be used during the performance of
radiographic examinations.
Use of the equipment for purposes other than those intended and expressly
stated by the manufacturer, as well as incorrect use or operation, may relieve the
manufacturer or his agent from all or some of the responsibility for resultant non-
compliance, damage or injury.
MAIN COMPONENTS
See Figure 1-1. The Q-DRT Trays contain:
1. Detector tray cover (Wall Stand models only)
2. Phenolic Panel (Wall Stand models only)
3. Sliding drawer (wall stand with left load shown)
4. Drawer slide handle
5. Portable detector locking retainer and spring block
6. Heavy duty drawer slide system
7. Detector tray turntable (rotating models only)
8. Removable grid and ion chamber (optional).
3 1
2
5
6 7
Note:
1. A cable guide for tethered receptors is provided on certain models
(location varies with tray model).
SPECIFICATIONS
2-1
2-2
Chapter 2 Specifications
PRODUCT SPECIFICATIONS
The following are specifications for Q-DRT Trays, which are compatible with
Quantum QW-420 Wall Stands and QT-740 and QT-750 Radiographic Tables.
GENERAL SPECIFICATIONS
Design
ENCLOSURE: Four detector tray models (see Table 1-1)
Material and Finish: Aluminum base with powder coat steel cover.
PHYSICAL CHARACTERISTICS
The following table describes the physical characteristics of four Q-DRT Tray
designs:
Weight
Detector Style Overall Dimensions
(without detector)
Rotating
Table: 584 mm (W) x 559 mm (H) x 73 mm (DP)
Varian 23.0 in. (W) x 22.0 (H) x 2.87 (DP) 18 kg (40 lb)
4336
Wall Stand: 561 mm (W) x 612 mm (H) x 79 mm (DP)
22.1 (W) x 24.1 (H) x 3.1 (DP) 21 kg (48 lb)
Rotating
Table: 584 mm (W) x 559 mm (H) x 73 mm (DP)
Carestream 23.0 in. (W) x 22.0 (H) x 2.87 (DP) 18 kg (40 lb)
DRX-1
Wall Stand: 561 mm (W) x 612 mm (H) x 79 mm (DP)
22.1 (W) x 24.1 (H) x 3.1 (DP) 21 kg (48 lb)
Rotating
Table: 584 mm (W) x 559 mm (H) x 73 mm (DP)
Vatech 23.0 in. (W) x 22.0 (H) x 2.87 (DP) 18 kg (40 lb)
(Samsung)
Wall Stand: 561 mm (W) x 612 mm (H) x 79 mm (DP)
22.1 (W) x 24.1 (H) x 3.1 (DP) 21 kg (48 lb)
Weight
Detector Style Overall Dimensions
(without detector)
Rotating
Table: 584 mm (W) x 559 mm (H) x 73 mm (DP)
Vieworks 23.0 in. (W) x 22.0 (H) x 2.87 (DP) 18 kg (40 lb)
ENVIRONMENTAL SPECIFICATIONS
The following are environmental specifications for Model Q-DRT Image Detec-
tor Tray:
System Operating Environment
Ambient
Temperature: +10 ° C to +40 ° C (+50 ° F to 104 ° F)
Relative
Humidity: 30 to 75%, Non-condensing
Atmospheric
Pressure: 700 hPa to 1060 hPa
Non-Operating Environment
Ambient
Temperature: -18 ° C to +70 ° C (-0.4 ° F to 158 ° F)
Relative Humidity: 20 to 95%, non-condensing
Atmospheric
Pressure: 500 hPa to 1060 hPa
COMPATIBILITY STATEMENT
The Quantum Medical Imaging, LLC Digital Image Detector Trays, marketed under
the Q-DRT designation, are compatible with all Quantum Medical Imaging, LLC Model
QW-420 Series Wall Stands, and Models QT-740 and QT-750 Fixed and Elevating
Radiography Tables.
ASSEMBLY &
INSTALLATION
3-1
3-2
Chapter 3 Assembly & Installation
OVERVIEW
The Model Q-DRT Series Trays for Model QW-420 Wall Stands, and QT-740 and QT-
750 Radiographic Tables are completely installed and tested at the factory prior to
shipment. Therefore, all relevant unpacking, and assembly and installation instruc-
tions for Q-DRT Trays are found in the respective Table or Wall Stand Service Manuals
DC30-007 or DC30-002. Refer to Chapter 4, OPERATION, of this manual for details as
to proper use of the Q-DRT Trays installed on the specific table or wall stand ordered.
OPERATION
4-1
4-2
Chapter 4 Operation
TO RELEASE TRAY
LOCK, PUSH IN ON
DETECTOR TRAY
HANDLE, UNTIL A
"CLICK" IS HEARD.
THEN PULL TRAY OUT
UNTIL ANOTHER
"CLICK" IS HEARD
(AT FULL EXTENSION)
SPRING-LOADED
RETAINER
FIXED
RETAINERS
CLAMPING
RETAINER
Figure 4-3. Q-DRT Rotating Tray with Detector Installed - Portrait Orientation
4. While maintaining pressure against the fixed retainers, move the
handle of the Detector toward the floor of the tray, to seat it in
front of the spring-loaded retainer and the clamping retainer clos-
est to the Detector handle (see Figure 4-3).
5. Set the clamping retainer to lock the Detector in place. The
Detector is prepared for a portrait exposure.
6. If necessary (for landscape exposure), and while the tray is fully
extended, rotate the detector handle downward for right-loading
configurations, or upward for left-loading configurations, until the
tray enters the detent. The foregoing procedures should result in
secure mounting of the Detector, allowing for the tray to slide
back into its tray, set for the desired orientation.
DETECTOR
CABLE
GUIDE IN
RETAINER
(Not
applicable if
wireless
detector)
POSITIONING
RETAINERS
Figure 4-7. Q-DRT Rotating Tray with Detector Installed - Portrait Orientation
3. To remove the grid panel, move the handle in the direction indicated by the
arrow, until it stops, then, withdraw the grid assembly from the cover.
4. While the grid is not in use, store it carefully to protect the grid surface, and
the symmetry of the frame.
Phenolic Panel
(rear surface)
MAINTENANCE
5-1
5-2
Chapter 5 Maintenance
OVERVIEW
The Q-DRT Digital Detector Trays will function reliably with virtually no mechanical
maintenance, however a list of wear parts is provided in this section.
USER MAINTENANCE
The equipment user is responsible for the basic cleanliness of the equipment. On
a regular basis, the Q-DRT Tray, along with Radiographic Table or Wall Stand to
which it is mounted, should be wiped clean. Painted metal surfaces should be
cleaned using a clean cloth slightly moistened in warm soapy water (use mild
soap). Wipe with a clean wet cloth. Use only alcohol-based liquid disinfectants.
PLANNED MAINTENANCE
Routine inspection of the Q-DRT tray should be performed by qualified service
personnel on an annual basis.
A complete series of inspections and functional checks was conducted at the time
of installation to insure proper operation of the system. The following inspection
and adjustment procedures are recommended to maintain the system in its origi-
nal operating condition.
• Check for evidence of loose hardware
• Check all bearings and bearing surfaces for cleanliness and corrosion
• Conduct a general inspection for worn or damaged parts
• Visually inspect for wear and cleanliness
REPLACEMENT PARTS AND ORDERING INFORMATION
Table 5-1 provides a list of replaceable parts for Q-DRT Rotating Trays. Figures
5-1 and 5-1a show the locations of the replaceable parts described therein.
Removal and replacement instructions are provided as required.
ORDERING INFORMATION
To order replacement parts for the Q-DRT Tray, contact the Service
Department at:
Quantum Medical Imaging, LLC
2002-B Orville Drive North
Ronkonkoma, New York 11779 USA
Phone: (631) 567-5800 (x2)
Fax: (631) 567-5074
e-mail: qmiservice@carestream.com
When ordering replacement parts, supply the following information:
• Model, reference, and serial number of equipment
• Part number
• Part description
• Quantity required
• P.O. Number
• Shipping Instructions
When ordering components or parts not listed in Table 5-1, a complete description
of the part, including its function and location should be provided with the model
number and serial number of the unit.
6 Tray Handle 1
Rotating Models ME10-681
* As required
5
2
3
4
2 7
8
6 9
T:\Storage\Manuals\Q-DRT Series Casette Trays\Installation - Operation Manual\Replaceable Parts - Q-DRT Rotating Tray.cdr
10
T:\Storage\Manuals\Q-DRT Series Cassette Trays\DRAWINGS\Q-DRT Rotating Housing\Q-DRT Rotating Housing - Grid Assy - Spare Parts.cdr
DETENT
PLUNGER
DETENT
BUMPER
Figure 5-2. Detent Bumper and Plunger Assembly (Two Per Tray)
4. Remove the worn bumper, by removing one Phillips Flat Head
screw (see Figure 5-2).
5. Install the new Detent Bumper and secure it with the same Phil-
lips Flat Head screw removed in previous step.
6. Position the Rotating Tray on the Sliding Tray, making sure that
the Detent Wheel mounted to the bottom of the Rotating Tray is
positioned between the two Detent Bumpers, then align the thru-
holes in the Rotating Tray with the tapped holes in the Turntable.
Secure the Rotating Tray to the Turntable, using three (3)
5/16-18 x 1/4" undercut Flat Head screws.
7. Inspect the installation by rotating the Tray through it’s entire
range of motion (detent to detent).
8. Ensure that the Rotating Tray is in its Portrait detent position, and
release the Sliding Tray catch by gently pulling out on the handle,
then pushing the handle in to close the drawer slide into the Tray.
9. Reinstall the assembled Q-DRT Tray on the vertical trolley of the
wall stand.
Removal and Replacement of the Sliding Tray Latch (Rotary
Models Only)
This procedure requires that the portable DR detector be removed from
the Rotating Tray. Proceed as follows:
1. Refer to Removal and Replacement of Detent Bumpers procedure
(steps 1 through 3) for instructions for gaining access to the Slid-
ing Tray Latch.
2. Once the disassembly of the Sliding Tray has been completed,
remove four (4) 4-40 x 1/4" Pan Head screws securing the Latch
to the floor of the Sliding Tray, and lift the Latch assembly out or
its position, noting its orientation before removal (see Figure
5-3 below).
3. Position the replacement Latch (in the same orientation as the
original Latch) over the through holes, and re-install four (4) 4-40
x 1/4" Pan Head screws.
REAR WALL OF
HOUSING
LATCH
KEEPER
LATCH
MECHANISM
DOUBLE -SIDED
TAPE
(1" x 3-1/2")
P/N: CS30-008
BOTTOM
VIEW
Figure 5-5. Q-DRT Wall Stand Tray Chin Rest - Final Installation
LOCATION OF PUSH/
PULL CATCH
HARDWARE
PUSH/PULL
CATCH AND
SHROUD (2X)
Figure 5-6. Q-DRT Rotating Model - Slide Tray Shown without Rotating Tray
2. Once the screws holding the Catch to the Sliding Tray have been
removed, slide the Catch out from under the Tray.
3. The replacement part should be slid into position via the same
access point, and aligned with the through holes in the floor of
the Tray.
4. Install the Catch and Shroud with four (4) 4-40 x 3/4" (82°) Flat
Head screws.
5. Inspect the functionality of the Sliding Tray with the new Catch,
then reassemble the unit, using the instructions provided in
Removal and Replacement of Detent Bumpers in this section
(steps 6 through 9).
Removal and Replacement of Receptor Lock Micro Switch (Table
Models Only)