™
Models QT-740 QT-740 and QT-750 QT-750
Fixed/Elevating Float-Top R adiograph ic Tables Tables Operator’ Ope rator’ss M anual
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 I maging, LLC 2002-B Orville Drive North Ronkonkoma, New York 11779 USA Phone: (631) 567-5800 Fax: (631) 567-5074 E-mail: info@qmitea m.com www.quantummedical.net
Made in U.S.A.
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
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10/27/09
Incorporate ECO 2011, 2092
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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
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Chapter
1
S A F E T Y N OT I C E S
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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
CAUTION
NOTE
Indicates injury or death is possible if the instructions are not obeyed. Indicates that damage to equipment is possible if the instructions are not obeyed.
Indicates essential information that should be read to avoid incorrect operation.
WARNING Quantum M edical Imaging, LLC disclaims all responsibility responsibility from any injury resulting from improper application of this equipment. This equipment is sold to be used exclusiv ely under the prescribed direction of a person who is licensed by law to operate equipment equipment of this nature. This equipment mu st be used in accordance w ith all safety procedures described described in this m anual and must not be used for purposes other than those described herein. Quantum M edical Imaging, LLC cannot assume responsibility responsibility for any malfunctioning of this equipment resulting from improper operation, maintenance, or repair, or from damag e or modification of its compon ents.
X-RAY PROTECTION X-rays are hazardous to both patient and operator unless established safe exposure factors and operating instructio ns are observed. It is important that everyone having anything to do with x-radiation be properly trained trained and fully acquainted with the recommendations of the National Council on Radiation Protection and M easurements as published
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Chapter 1 Safety Notices
in NCRP R eports available available from from NCRP Publications, 7910 W oodmont Avenue, Suite 800, Bethesda, Bethesda, Maryland 20814-3095 (ww w.ncrp.com), w.ncrp.com), and of the International Comm ission on Radiological Protection (ww w.icrp.org), w.icrp.org), and take adequate steps to protect against injury. X-ray equipmen t may cause injury if used improperly. The The instructions contained in this manual must be read and followed w hen operating this unit. Personal radiation m onitoring 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 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. 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 replaced in the future. Those authorized to operate, 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 X-Ray Systems and Their Major Components," and NCRP Report No. 102, “Medical X-Ray, 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. 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. 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
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Chapter 1 Safety Notices
EU Authorized Representative: Medizintechnik Berlin GmbH Altentreptower, Strasse 59 12683 Berlin - Germany Phone: +49-302-82 4726 Fax: +49-302-82 6382 E-mail:
[email protected] The following symbols may be used for marking on this equipment or equipment documentation: 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 Fixed/Elevating FloatTop Radiographic Tables Service Manual, document number DC30-007.
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Chapter
2
GE NE RA L INFORMATION
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Chapter 2 General Information
OVERVIEW
NOTE
The user should read this manual in its entirety prior to using this equipment. It should be kept in a location near the equipment and readily accessible to the those that operate it.
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 radiographic table). 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 key features of Model QT-740 and QT-750 radiographic tables are as follows: •
Large Large Table Tabletop top area area (85 (85 inches inches long long x 35.55 35.55 inch inches es wide) wide) prov provide idess ample ample examination platform
•
Four-way Four-way floating floating tablet tabletop op permits permits 30.5 inches of longitu longitudinal dinal travel travel and 10 inches of lateral travel for full radiographic coverage
•
Foot pedal controls controls for for table table float-top float-top motions motions (foot (foot pedal pedal inhibit inhibit switch deactivates foot pedals to prevent inadvertent tabletop motion)
•
Float Float Handl Handle e Assembl Assembly y with with FLOAT FLOAT push push butto button n contro controll is provi provided ded for for operator convenience
•
Small patient-topatient-to-film film plane distance distance provides provides improved improved radiography radiography with minimal magnification
•
Accepts Accepts all all types types of image image receptors receptors (buckies, (buckies, grids, grids, and and station stationary ary grid cabinets)
•
Pati Patien entt hand handgr grip ipss are are stan standa dard rd acc acces esso sory ry
•
AC line line cord, cord, fitted fitted with with hospi hospital tal-gr -grade ade plug plug,, plugs plugs into into a 115VAC, 115VAC, 50/60 50/60 Hz receptacle (optionally field wired). Also configurable for 230 VAC, 50/60 Hz power input.
•
The Image Image Receptor Receptor Cabinet Cabinet is equipped equipped with electric electric locks locks ensuring ensuring precise precise film receptor alignment
In addition, the Model QT-750 provides: •
Heavy-duty Heavy-duty lift mechanism mechanism allows allows for patient patient loads loads of of up to 650 lbs.* (weight (weight must be centered over table base)
•
Variable Variab le height height tabl tableto etop, p, lowers lowers to to 21 inches inches and rais raises es to 32.5 32.5 inches inches (11.5 (11.5 inches total vertical travel)
•
Foot Foot pedal pedal and hand hand contr controls ols for table table up/dow up/down n motio motions ns
•
Obstru Obstructi ction on sensor sensorss disabl disable e tablet tabletop op down down motion motion in the the event event an 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 Tables are intended for use as a patient support device during the performance of radiographic examinations.
Models QT-740 & QT-750 - Operator’s Manual Quantum Medical Imaging, LLC
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MAIN COMPONENTS See Figure 2-1. The radiographic radiographic table contains: contains: 1
Patient Handgrips
2
Tabletop
3
Imag Image e Rec Recep epto torr Loc Lock k Rel Relea ease se Swit Switch ch
4
Cont Contro roll Han Handl dle: e: FLOAT FLOAT Push Push Butt Button on Swit Switch ch
5
Contro Controll Hand Handle: le: UP/DOWN UP/DOWN Rocker Rocker Switch Switch (Model (Model QT-750 QT-750 only) only)
6
Foot Foot Peda Pedal( l(s) s) - Flo Float at (Mod (Model el QT-7 QT-740 40)) Float, Up and Down (Model QT-750)
7
Table Base
8
Foot Foot Peda Pedal/ l/FL FLOAT OAT Push Push Butt Button on Inhi Inhibi bitt Swi Switc tch h
9
Emer Em erge genc ncy y Shut Shut-o -off ff Swit Switch ch (Mo (Mode dell QT-7 QT-750 50 onl only) y)
1
2
3
4
5
9
6
8 7
Figure 2-1. Radiographic Table Main Components
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Chapter
3
O OP PE ER RA AT TIIO ON N
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Chapter 3 Operation
OVERVIEW To provide precise patient positioning, Models QT-740 and QT-750 QT-75 0 radiographic tables feature a table top that "floats" in four directions; transversely (forward and backward) and longitudinally (left and right). right). Model QT-750 has the addiadditional capability of table top elevation (i.e., the table top can be raised and lowered 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 w ith reasonable care. Manufacturer’s equipment recommendations described described in this m anual must be observed. 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 w hen table top is not centered. 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. WARN ING! Do not allow patient to place place his/ 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 feature a "floating" table table top. With the "floating" table top function activated, both transverse and longitudinal positioning of the patient is enabled. To operate the float-top float-top function, proceed as follows: WARN ING! When transferring 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.
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1. Position Position the the patient patient on the table with with his or or her hands hands situated situated along along the side 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 Press the FLOAT FLOAT Foot Pedal Pedal or the the FLOAT FLOAT push button button on the Table Table Control Control Handle to enable transverse and longitudinal motion of the table top (see Figures 3-2 through 3-4).
FLOAT Foot Pedal
Figure 3-2. Model QT-740 FLOAT Foot Pedal Control
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Chapter 3 Operation
3. Releasing Releasing the FLOA FLOAT T Foot Pedal Pedal or the the FLOAT FLOAT push button button (located (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
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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 Disable Switch is provided. 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 the switch light is illuminated disables all Foot 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
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Chapter 3 Operation
ELEVATING MOTION (MODEL QT-750 ONLY)
NOTE
The Model QT750 table is equipped with Obstruction Sensors, which detect the presence of an obstruction below the table top when the table top is being driven downward. This feature is only designed to avoid damage to the table and is not intended as a safeguard against personal injury.
On Model QT-750 radiographic tables, the elevation function allows the table top to be lowered down to as low as 21 inches (533.4 mm) from floor, floor, up to a working height of 32.5 inches (825.5 mm). To operate the table top elevation elevation function, proceed as follows: WARN ING! For safety purposes on Model QT-750 tables, an Emergency Stop Switch (see Figure 3-6) w hen activated immediately removes power from the table top up/dow n motor. Rotating the Emergency Stop Switch knob 1/4-turn counter-clockwise releases the Emergency Stop Switch and restores restores up/dow n motor power.
EMERGENCY STOP SWITCH (MODEL QT-750 ONLY)
Figure 3-6. Emergency Stop Switch Location
IM PORTAN T! On Model QT-750 QT-750 tables equipped with Digital Receptor Drawer Slide Option (QTDDS): Table top up or down motion is disabled when the digital receptor drawer slide is extended out from under the table top. Push receptor receptor in fully to enable up or down m otion.
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UP PEDAL
DOWN 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
LOWERI NG THE TABLE TOP 1. It is recomme recommended nded that that the table top be center centered ed before before lowerin lowering g it (refer to table top Float Motion operation described in preceding paragraph). 2. Press the the DOWN Foot Foot Pedal Pedal (see (see Figure Figure 3-7) or, or, on the Control 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. Tran ransfe sferr patien patientt onto onto table table top. top.
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Chapter 3 Operation
4. Ensure Ensure patient patient is positioned positioned with with his or or her hands hands situate situated d along the side of their body, body, or with the hands grasping the patient handles (see Figure 3-1). Be sure patient’s hands remain above the table top. RAI SIN G THE TABLE TABLE TOP 1. Press Press the UP Foot Foot Pedal Pedal (see Figure Figure 3-7) 3-7) or, or, on the Control Control HanHandle (see Figure 3-8), press the Table Top Top Rocker Switch toward the up arrow to raise the table top to the desired height. 2. Proce Proceed ed with with exam examin inat atio ion. n. IMAGE RECEPTOR CABINET LOCK
The Image Receptor Cabinet rides on four linear ball-bearings mounted to adjustable brackets attached attached to either side of the cabinet. These bearings travel on the hardened and polished steel steel shafts of the Receptor Cabinet Carriage. Carriage. An electromagnet 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, tray, depending on the system ordered. The following paragraphs describe the operating instructions for each. Additional information is contained contained in the cassette tray manufacturer’s documentation, which is provided with the table.
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Loading Cassette Tray (Midw est Type) To load a film cassette into a "Midwest" type cassette tray, proceed as follows: 1. Float Float the table table top top full fully y back. back. 2. Pull cassett cassette e tray tray from recept receptor or using tray tray handle handle (see (see Figure Figure 3-10). 3. Pull back back on on front front cassett cassette e grip to open open both both grips. grips. 4. Position Position slide slide guides guides ("L" bracket bracketss seated seated in channels) channels) to casset cassette te size using indicators on cassette tray (press center brass button to allow movement). 5. Insert Insert casset cassette te into into tray (back end first). first). 6. Lock Lock cass cassett ette e into into tray tray.. 7. Push Push front front grip grip again against st cass casset ette. te. 8. While pushing pushing front front grip grip against against cassette cassette,, turn cassette cassette lock lock handle to lock position. 9. Push tray tray into recept receptor or.. The cassette cassette is is now in exposure exposure position position..
SLIDE GUIDES
CASSETTE GRIP LOCK HANDLE
TRAY HANDLE
Figure 3-10. Midwest Cassette Film Tray
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Chapter 3 Operation
Loading Cassette Tray (Poersch Type) To load a film cassette into a "Poersch" type cassette tray, tray, proceed as follows: 1. Float Float the the tabl table e top top full fully y back back.. 2. Pull cassett cassette e tray tray from recept receptor or using tray handle handle (see (see Figure Figure 3-11). 3. Place thumb under lip of clamp clamp handle. handle. Lift handle to releas release. e. 4. Grasp Grasp handle handle and slide slide clamp clamp back back for inserting inserting cassett cassette. e. 5. Insert Insert cassett cassette e into into tray tray (back (back end first). first). Center it using using center center-ing label. 6. Slide clamp forwa forward rd pushing pushing clamp clamp firmly firmly against against cassette. cassette. 7. While pushing pushing clamp against against cassett cassette, e, press press clamp clamp handle handle down.
CLAMP HANDLE
TRAY HANDLE
Figure 3-11. Poersch Cassette Film Tray
Models QT-740 & QT-750 - Operator’s Manual Quantum Medical Imaging, LLC
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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 operation of the digital imaging 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
WARN ING! Keep fingers fingers away 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.
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Chapter 3 Operation
Digital Receptor (Extended)
RECEPTOR LOCK HANDLE
Figure 3-13. Digital Image Receptor - Extended Position
WARN ING! Do not apply a load of more than 32 lbs. (14.5 (14.5 kg) on the image receptor when it is in the extended position; the unit may be collapse. WARN ING! On Model QT-750 QT-750 tables 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 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 un til the desired lateral lateral receptor position is attained. Release the Receptor Receptor Lock Handle to lock the receptor in its current position.
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CXDI-50G DIGITAL DIGITAL RECEPTOR CABINET OPTION (T YPE 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 X-ray table applications. The RT-DOK50-T RT-DOK50-T option provides a rotating tray that allows the X-ray X-ray TechTechnician to change receptor orientation without removing the receptor from the tray. Detailed instructions for operation of the RT-DOK50-T 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 DIGITAL RECEPTOR CABINET OPTION (TYPES Q-DRT-CT AND Q-DRT-CT-R)
Quantum offers rotating and non-rotating receptor tray models for Canon CXDI50G digital receptors used in QT-740 QT-740 and QT-750 X-ray X-ray table applications. applications. The non-rotating version (Q-DRT-CT) (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) (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 Q-DRT-CT and Q-DRT-CT-R Q-DRT-CT-R are available in document DC30-093 (shipped with the X-ray table).
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Chapter
4
USER MAINTENANCE
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Chapter 4 User Maintenance
OVERVIEW This chapter is designed to assist the system user in maintaining the smooth operation 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 representative. 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: •
Visual Visually ly insp inspect ect the table table for for wear wear and and clea cleanli nlines nesss
•
Clean the tableto tabletop, p, cassett cassette e tray, tray, and and exteri exterior or painted painted surfaces surfaces of the the table table
•
Disinfect Disinfect the table table top surfac surface e after after each use in in accordanc accordancew ew with with facili facility ty 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 sursurfaces should be cleaned using a clean cloth slightly moistened in warm soapy water (use mild soap). Wipe with a clean wet cloth, then dry. dry. Never use abrasive polish on this equipment. WARNING! Always disconnect the equipment from the main pow er 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 m ain disconnect (or power cable) on systems w ired directly directly to facility power. To remove the cassette tray from the Receptor Cabinet for cleaning, proceed as follows: Midwest Trays
1. Float Float the table table top fully fully back. back. 2. Pull the the cassett cassette e tray tray out out by the handle handle until it stops. stops. 3. Grasp Grasp both sides of of the tray tray with your your right right hand hand placed placed near the the table table and your left hand towards the tray front.
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4. Locate Locate the spring-load spring-loaded ed lever lever on on the right side of the the tray tray bottom. bottom. A spring-loaded plate covers covers this hole. Press the lever with your right index finger, finger, lift the cassette tray up slightly and pull the tray away from the Receptor Cabinet. Poersch Trays
1. Float Float the table table top fully fully back. back. 2. Pull the the cassette cassette tray tray out by the handle handle until until it stops. stops. 3. Grasp Grasp the left side of of the tray tray with with your left hand. hand. 4. Locate Locate the square block at the the back right side of the the cassette cassette tray. 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 (Quantum option RT-DOK50-T) RT-DOK50-T) is described in detail in document User and Installation 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 Q-DRT-CT and Q-DRT-CTQ-DRT-CT-R R digital receptor trays are described in detail in document DC30-093 (shipped with the X-ray Table).
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Chapter
5
WARRANTY INFORMATION
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Chapter 5 Warranty 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 warranty extend beyond 15 months from the date of shipment. If the attached warranty 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 per system or major component purchased. WARRANTY CARD
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Clip or Copy Warranty Card on reverse side and submit to QMI
See Reverse Side for Warranty Card
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Chapter 5 Warranty Warranty Information
WARRANTY STATEMENT (Continued) Promptly complete the warranty card and mail or fax it to: Quantum M edical Imaging, LLC 2002-B Orville Drive Drive North Ronkonkom a, N.Y. 11779 USA 631 567-5074 567-5074 fax fax 631 567-5800 567-5800 voice 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. 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 distributor or reseller, reseller, are warranted exclusively by their manufacturers according to each of their independent warranty terms and conditions. Warranty 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 statutory.. NO IMPLIED WARRANTY WARRANTY OF MERCHANT ABILITY OR FITNESS FOR A PARTICULAR PARTICULAR PURPOSE SHALL APPLY. APPLY. Quantum Medical Imaging, LLC Warranty is exclusive of: 1) Failure Failure of the the Buyer/Deale Buyer/Dealerr to prepare prepare the site site and operating operating environ environment ment in accordance with applicable instructions and recommendations of QMI. 2) Failure Failure of Buyer/Dea Buyer/Dealer ler to provide provide the proper proper incoming incoming power require required d to support the equipment in accordance with the requirements of QMI. 3) Modificati Modification on of QMI products products perfor performed med by a party party other than QMI. QMI. 4) Combining Combining produc products ts deemed deemed by QMI QMI to be incompa incompatible tible.. 5) Improper Improper or extrao extraordina rdinary ry use of a product, product, improper improper maintena maintenance nce of the prodproduct, or failure to comply with any applicable instructions and recommendations of Quantum Medical Imaging, LLC. 6) Misuse, Misuse, abuse, abuse, tampering, tampering, or negligent negligent storage storage or handling handling of a product product by the the Buyer, Buyer, its employees, agents, or o r contractors. 7) Fuses, Fuses, glassware, glassware, high high voltage voltage cables cables and other other items items deemed deemed by QMI to be be expendable. Acts of God, fires, floods, power failure failure or electrical power surges. surges. Strikes, sabotage, labor disturbances, war, war, riots, acts of civil or military authority, authority, or other causes beyond the reasonable control of QMI. Installation, routine troubleshooting and repair are also excluded from warranty. warranty. Technical service and maintenance is the responsibility of the Dealership selling the equipment.
Models QT-740 & QT-750 - Operator’s Manual Quantum Medical Imaging, LLC
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Chapter 5 Warranty Information
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 repairing,, adjusting, adjusting, or replacing replacing any defecti defective ve or non-conformi non-conforming ng component component or product. B) By making making available available any necessary necessary repair repair or replacem replacement ent parts or assembli assemblies es for exchange. Quantum Medical Imaging, LLC shall have the option to furnish either new or rebuilt replacement parts or assemblies for exchange. exchange. All returned parts shall 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, warranty, whether the claim is on contract, warranty, 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. 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 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. Form. All freight charges resulting from Warranty Warranty Returns are are the responsibility of the Buyer/Dealer.
EQUIPMENT IN TRANSIT QMI assumes no responsibility for equipment damaged damaged in transit to or from QMI. To protect the Buyer/Dealer, Buyer/Dealer, the receiver of any equipment should examine all cartons and crates carefully at the time time of delivery. delivery. If damage is apparent, make a notation notation on the delivery receipt, request an inspection by the freight carrier, 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) (Buyer/Dealer/Customer) is fully responsible for the filing of freight damage claims to the freight carrier. carrier. QMI assumes no responsibility for any loss or damage to products once they have been shipped from our factory 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.
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Chapter 5 Warranty Warranty Information
VOIDING WARRANTY Tampering with, or any attempt at installation, maintenance, repair, repair, service, relocation, or alteration of or to a QMI product, when performed by any person or entity other than Quantum Medical Imaging, LLC or its C ertified Dealer without the written approval of an Authorized Person at Quantum Medical Imaging, LLC, shall immediately Void and Cancel all warranties with respect to the affected product.
Models QT-740 & QT-750 - Operator’s Manual Quantum Medical Imaging, LLC
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