OEC Compact, 7600 Installation Procedure

Page 1
Compact / Series 7600
Mobile Imaging System
Installation Procedure
Part Number: 00-879039-03
April 1997
OEC Medical Systems, Inc.
384 Wright Brothers Drive
Salt Lake City, UT. 84116
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Compact / Series 7600 Installation Procedureii
This manual contains descriptions, instructions and
procedures that apply to the Compact / Series 7600 Mobile
Digital Imaging System only.
Refer to the Installation Repor t/Checklist P/N 00-879038-03
when installing a 7600 system.
Page 3
Compact / Series 7600 Installation Procedure iii
Revision History
Rev Dash Date Change Description Rev 1 -01 December 1995 Init ial Engineering Release Rev A -01 December 1995 Manufacturing Release Rev B -02 July 1996 Added power supply tolerances, kV tracking
specifications, and resolution specifications Rev C -03 April 1997 Add Series 7600 installation procedures Rev D -03 November 1998 Drawing change only
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Compact / Series 7600 Installation Procedureiv
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Compact / Series 7600 Installation Procedure v
TABLE OF CONTENTS
Introduction................................................................................................................... 1
Responsibility.............................................................................................................................1
Safety Procedures......................................................................................................................1
Explosion Hazard...................................................................................................................................... 1
Electrical Safety......................................................................................................................................... 2
Accident Reporting.................................................................................................................................... 3
Unauthorized Modifications....................................................................................................................... 3
System Specifications.................................................................................................. 4
Technical Specifications............................................................................................................................ 4
System Classification .................................................................................................................4
Connector Output Power............................................................................................................4
C-Arm........................................................................................................................................................ 4
Input Power................................................................................................................................5
X-ray Source Assembly..............................................................................................................6
Fluoroscopy............................................................................................................................................... 6
Pulsed Fluorography Mode....................................................................................................................... 6
Radiography.............................................................................................................................................. 7
Accuracy ................................................................................................................................................... 7
Video Signal.............................................................................................................................................. 7
Dimensions ............................................................................................................................................... 8
Tube Data And Rating Charts.....................................................................................................8
General Tube Data.................................................................................................................................... 8
X-ray Generator Information .......................................................................................................9
Unpacking and Inspection ......................................................................................... 10
Remove Protective Shipping Material....................................................................................... 10
De-pallet the System (Compact)...............................................................................................10
De-pallet the System (Series)...................................................................................................10
C-Arm...................................................................................................................................................... 10
Workstation............................................................................................................................................. 10
Installation................................................................................................................... 11
Site Requirements....................................................................................................................11
Installation Kit Contents............................................................................................................11
Cover Removal.........................................................................................................................12
C-Arm:..................................................................................................................................................... 12
Workstation:............................................................................................................................................ 12
Mechanical Checks..................................................................................................................12
Inspection and Setup................................................................................................................ 12
Line Voltage Compatibility Check............................................................................................. 13
Isolation Transformer Wiring.....................................................................................................13
Power ON System.................................................................................................................... 13
System Power Supply Voltages................................................................................................14
Measure Line Voltage Regulation.............................................................................................14
System Operational Verification ............................................................................................... 15
Generator................................................................................................................................................ 15
Workstation............................................................................................................................................. 18
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Compact / Series 7600 Installation Procedurevi
Thermal Printer / Multiformat Camera........................................................................20
Fluoroscopic Image Tests.........................................................................................................21
Radiographic Beam Alignment Test..........................................................................................21
Setup....................................................................................................................................................... 21
Beam Alignment Verification................................................................................................................... 21
Complete Paper Work...............................................................................................................22
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Compact / Series 7600 Installation Procedure 1

Introduction

This manual describes the installation of the Compact / Series 7600 system and a definition of the responsibilit ies and instructions for reporting, safety, unpacking, moving and verifying system operat ion.

Responsibility

The customer must provide the labor and equipment necessary to unload the system from the transport vehicle and move it to t he final location. It is the customer’s responsibility to obtain all permits necessar y to m eet all requirements of stat e and local codes, regulations and ordinances with respect to the installation and operation of the system.
A qualified service technician should perform the following:
Installation Report/Checklist (00-879038-03).Safety procedures should be in effect at all times dur ing the installation process. By law, complete reports within 15 days from the date of assem bly (installation).
Return the assembler's copy of the Report of Assembly of Diagnostic X-ray (FDA form 2579), the Beam Alignment Radiographs (films), and the Installation Report/Checklist t o O EC Medical Systems, Inc., Attention: Technical Support, in the stamped, manila envelope provided in the Field Service Documentation Package.
Distribute the various remaining copies of the Report of Assem bly of Diagnostic X-ray (FDA form 2579) , following the documentation instructions included in the Field Service Documentation Package.
The OEC Medical Systems, Inc. Representative MUST sign the last page of the Installation Report and Checklist, verifying Field Service acceptance of the unit. If, for any reason, the installation remains incomplete, notify the Hospital that the system is not yet ready for use.
NOTE

Safety Procedures

Under no circumstances should the safety interlocks in the system be bypassed, jumped or otherwise disabled. Never operate or store the system in a location where conductive fluids such as water, saline solution, etc., can spill on any part of the equipment unless you cover the system with a protective waterproof draping.
: All OEC Medical Systems, Inc. systems comply with International
Electrotechnical Commission safety standard IEC- 601. Do not connect any external device to the system that does not meet the req uir em ents of IEC-601. Only devices provided by or approved by OEC Medical Systems, Inc. should be connected to the system.

Explosion Hazard

Never operate the system in the presence of f lam m able anesthetics or other flammable or explosive liquids, vapors, or gases. Vapors and gases can ignite by electrical arcs that can occur during the normal operation of switches, circuit breakers, push-buttons and other cir cuit com ponents.
Page 8

Electrical Safety

el
Grn
PROTECTIVE EARTH SMBOL PROTECTIVE EARTH STUD
WARNINGS:
Compact / Series 7600 Installation Procedure2
If flammable substances are pr esent before you apply system power, do not plug in or turn on the system.
If you detect flammable substances after the system has been turned on, do not touch any of the controls, switches, knobs or cables. Evacuate all per sonnel immediately, then ventilate the room to clear t he air of the flammable vapor or gas. Remove any volatile liquids that are producing flammable vapors to a safe storage area.
Electrical circuits inside the equipment use voltages that are capable of causing serious injury or death from electr ical shock.
This equipment contains high power elect ri cal components and only personnel familiar with the circuitry and its operation should provide service. Some components may maintain a charge with the power cord disconnected.
Observe safety precautions when measuring high voltage electronics. Steps within this procedure produce x- rays. Use appropriate precauti ons.
Areas where hazardous voltages exist include:
Transformers - 100 - 240 volts Video Monitors - 100 - 240 volts and High AC/DC Voltages Image Intensifier - 50,000 volts Generator - 110,00 volts
Observe the following precautions when you remove system covers:
Observe the two person rule when working near lethal voltages. A person
who is familiar with the emergency power removal procedure must be in attendance. This person must remain clear of the machine and be prepared to turn it off in an emergency.
Be familiar with the components being serviced and the locations of hazardous voltages in the assembly where you work.
High voltage cables and capacitors can retain a charge even when you remove all power from the system. Avoid touching these unless you are certain the charge has dissipated to gr ound.
Some high energy capacitors in the system should be shorted to ground through an adequate resistance to avoid a burn hazard.
A protective earth ground stud, located on the bottom left side of the system base, and marked with the international symbol shown below on the left. It also has a distinctly colored decal at t he base of the stud as shown below on the right.
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Compact / Series 7600 Installation Procedure 3

Accident Reporting

The Medical Device Reporting Regulation, 21 CFR Part 803, r equires that the manufacturers of medical devices submit a report to the appropriate f ederal agency containing specific infor m ation in the event of an accident resulting in death or serious injury during the use or service of it s medical devices. (In the following paragraphs, labeling definitions include all instructional and procedural text contained in the Operator's Guide and Periodic Maintenance Procedures.)
A report is not necessary if:
The potential for death or t he type of serious injury that may result appears in the labeling for the system.
The malfunction and the rout ine ser vice, r epair , or maintenance in­structions to correct the problems appear in t he labeling for the system.
The malfunction has occurred at or below its expected rate of frequency and severity.
The malfunction does not lead the manufacturer to undertake a r em edial action involving any other systems.
For OEC Medical Systems, Inc. to meet these report ing r equirem ents, all users of these systems, operators, and service technicians, must provide the QA Manager of OEC Medical Systems, Inc. with the following information reg arding all reportable events as soon as possible:
1. Ident ify the model and the serial number.
2. Describe the event. I nclude whether any serious injury or death occurred, the number of personnel injured, and any publication tit le and dat es of any articles in the scientific or medical lit er at ure describing the reported event.
3. Identify the person who is submitting the information, include their address, to OEC Medical Systems, Inc.
4. Indicat e whether addit ional information will be submitted, and if so, when.
5. Indicate whether t he event being reported has occurred with greater frequency or severity than is indicated in the labeling for the system, or is unusual for this type of system.

Unauthorized Modifications

Unauthorized changes or modifications to any part of the system could have hazardous consequences. Changes or modifications are forbidden unless specifically authorized by OEC Medical Systems, Inc.
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Compact / Series 7600 Installation Procedure4

System Specifications

Technical Specifications

The policy of OEC Medical Systems, Inc. is one of continual product development and improvement. For this reason, OEC Medical Systems, Inc. reserves the right to change the operat ing characteristics and specifications of newer products at any time, without prior notice, and without incurring any obligation relating to previously manufactured items.
The specifications list limited t o general performance and physical data. Specifications of optional equipm ent provided by other manufacturers in the applicable manuals provided with those options.
OEC Medical Systems, Inc. will make available, on request, cir cuit diagrams, component part lists, descriptions, calibration instructions, or other information that will assist properly trained and qualified technicians to repair those parts of the system which are designated as repairable.

System Classification

Class I (as defined by IEC 601-1) Type B Ordinary protection against ingress of water Non AP (Non-anesthetic proof) Continuous operation

Connector Output Power

C-Arm

Footswitch: Handswitch:
15 VAC 30 milliamp current source 15 VAC 30 milliamp current source
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Compact / Series 7600 Installation Procedure 5

Input Power

NOTE:
The system operating voltage is changeable. If the operating voltag e r equires changing, the change may only be accomplished by an OEC Medical Systems, Inc. field service technician, or by qualif ied technical service personnel.
Line Frequency: 60/50 Hz Single Phase:
110V ~ Standby (long-time) 5 A, *Maximum (momentary) 25 A. 230V ~ Standby (long-time) 2 A, *Maximum (momentary) 15 A.
*Maximum (Momentary) rating is for maximum radiogr aphic exposure and limited to 4 seconds.
Resistance of Mains 0.6 ohms/230 ~
0.3 ohms/110 ~
Technique Factors at Maximum Line Current Condition: Peak current demand is independent of technique load factors.
Line Regulation (Percentage): 15% at maximum radiographic exposure. Also, under no conditions should the loaded voltage fall below 100 VAC, measured on the secondary of t he isolat ion transformer.
Maximum Continuous Power Dissipation: 4,253 BTUs. Figure based on a maximum real power value of 1, 245 watts.
NOTE:
Line regulation based on measurements made at t he input (primary winding) of the isolation transformer under standby conditions and at maximum radiographic exposure by the following equation:
Line regulation = 100 (Vn - Vl)/Vl Where Vn = no load voltage (standby)
Vl = loaded voltage (maximum radiographic exposure).
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Compact / Series 7600 Installation Procedure6
X-ray Source Assembly
Type Fixed anode type Focal Spot Dual, 0.6 mm and 1.5 mm Total Filtration >3 mm minimum aluminum eq uivalent Anode Heat
Storage Capacity 76,000 HU Leakage
Technique Factors 110 kVp and 3.0 mA Voltage Rating 110 kVp maximum

Fluoroscopy

Focal Spot Size 0.6 mm High Voltage Range 36 kVp to 110 kVp, with manual adjustment
available.
Current Range Standard 3 mA maximum
Dense Anatomy 6 mA maximum continuous
Snapshot 8 mA Duty Cycle: 110 kVp @ 6 mA maximum continuous Collimation Nominal diameter iris circle for 9/ 6 inch system
6 inches (15.2 cm), 9 inches (22.8 cm)
Iris collimation is continuously adjustable to
less than 5 x 5 cm, measured at the SID.
Slot collimation is continuously variable and
rotatable.

Pulsed Fluorography Mode

Focal Spot 0.6 mm kVp Range 36 kVp-110 kVp mA Range 0.2 - 8.0 mA Pulse Rate 1 pulse per second.
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Compact / Series 7600 Installation Procedure 7

Radiography

1.5mm Focal Spot High voltage range: 36 kVp t o 110 kVp Tube current 20 mA fixed.
Timer Duration of radiography can be manually set
from 0.1sec to 4.0 sec with an internal electronic timer.
Duty Cycle 110 kVp @ 20 mA maximum for 4.0 seconds. Collimation Nominal diameter iris circle for st andard 9-inch
(22.8cm) system, continuously adjustable to less than 5 x 5 cm, measured at the SID. A continuously variable and rotatable slot collimator is also standard.
Film Cassette Standard: 10 x 12 x 5/8-inch nominal. Holder Metric: 24cm x 30cm

Accuracy

kVp: + 10% mA: + 10% Timer: + 10%

Video Signal

Composite video, EIA RS170A 60 Hz, 525 line, [Internat ional CCI R 50 Hz, 625 line] 1 Vp-p
Single "C" mounted FastScan flicker-free monitor
30cm (12 inch) Standard 44cm (17 inch) Optional 20 MHz bandwidth

Workstation

Dual Monitors 44cm (17”) Fastscan, flicker-free monitor (100Hz) with anti reflect ion filter Image Rotation: 360 degrees 400 Image Memory wih last image hold X-Ray ON indicator lamp Patient annotation keyboard and control panel for system operation Integrated thermal printer (option) Integrated multiformat camera 2-on-1 or 1-on- 1 ( option)
Environmental and Transport Requirements
Ambient Operating: 10 to 35 degr ees C Temperature
Extended 0 to 40 degrees C Storage and Transportation
Short-term -10 to 55 degrees C Storage and Transportation
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Stability Positive stability on grades up to 10 degrees when in
transport position and on grades up to 8 degrees in any position
Altitude 8,000 ft. (2438 meter s ) m aximum Humidity Operating: 20 to 80%, non-condensing
Shock and Vibration 1 G at 5-200 Hz for 2 hours

Dimensions

Compact / Series 7600 Installation Procedure8
of normal use.
Storage and transport: 10%-90%, condensing
C-Arm
Workstation
Non-bracketed numbers are for the 17.8 cm/7-inch I.I. Numbers in brackets are for the 23 cm/9-inch I.I. Focus to top of generator housing: 205mm maximum w/o skinspacer. SID: 930 mm (37 inches) [905 mm] Free Space: 705 mm [680 mm] Central Beam to C-Arm: 660 mm (26 inches) C-Arm orbital motion: 115 degrees (25 degree overspan) C-Arm Rotation: +225 degrees C-Arm vertical motion: 420 mm . C-Arm horizontal motion: 190 mm . C-Arm Wig-wag: +10 degrees Length: 1630 mm Height: 1690 mm Width: 780 m m Weig ht : 245 Kg.
Length: 560mm Width: 660m m Height: 1665 Weig ht : 140kg

Tube Data And Rating Charts

General Tube Data

Maximum 110 kVp. Rated Tube Potential
Leakage 110 kV at 3. 0 mA. This is also the maximum continuous Technique rating of the X- r ay tube housing assembly. 110 kV at 3.0 Factors mA are the leakage technique factors used for the
diagnostic source assembly.
Total >3.0 mm minimum aluminum equivalent. Filtration
Anode Heat 76,000 HU Storage
Anode 330 HU/second maximum. Refer to the Thermal Maximum Characteristics curves in this section. Cooling Rate
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Compact / Series 7600 Installation Procedure 9

X-ray Generator Information

The X-ray Generator in the Com pact / Series 7600 complies with IEC 601-2­7/1987 and CSA 22.2 #601.2.7. The following information provided in accordance with these standards.
Reference: 601-2-7 Clause 6.8.2
1. Maximum mA @ Nominal kVp
Standard Fluoro 3 mA @ 110 kVp Dense Anatomy Fluoro 6 mA @ 110 kVp Pulsed Fluoro 3 mA @ 110 kVp Snapshot Fluoro 8 mA @ 110 kVp Film Mode 20 mA @ 110 kVp
2. Maximum kVp @ Maximum mA (See 1 above)
3. Maximum Output Power
Snapshot (Fluorography) 0.88 kW @ 110 kVp, 8 mA Film Mode 2.2 kW @ 110 kVp, 20 mA
4. Nominal Output Power for 0. 1 Second Exposure
Film Mode 2.0 kW @ 100 kVp, 20 mA
5. Reference mAs @ 50% of Nom inal O ut put Power
Film Mode 2.0 mAs @ 55 kVp
(20 mA, 0.1 second)
6. (Not Applicable)
7. (Not Applicable)
8. Nominal Shortest Exposure Time
Film Mode 0.1 second
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Compact / Series 7600 Installation Procedure10

Unpacking and Inspection

The customer should inspect the shipping containers and exposed system components for any apparent damage pr ior t o unpacking. Unpack any shipping containers that appear damaged with the carrier's agent present. The customer should ensure that all equipment specified in t he purchase order has been delivered.
If any part of the shipment shows damage or parts are missing, immediately notify the carrier and the nearest OEC Medical Systems, Inc. r egional service office. Retain the shipping container and packing material f or t he carrier's inspection.
Use the Installation Report/Checklist for reporting shipping dam age to the equipment. Indicate the location of damage on the drawing view or views as appropriate and describe parts lost or damaged in shipment.

Remove Protective Shipping Material

1. Remove the banding from the shipping carton(s) .
2. Remove the cardboar d cap( s) and lift the cardboard fr om the top of the unit(s). Discard the cardboard.
3. Remove the tape and packaging.

De-pallet the System (Compact)

1. Remove the thr ee u- shaped metal brackets that hold the system to t he pallet.
2. Remove the tape or banding that attaches the x-ray tube to the metal brace on the front of t he pallet.
3. Carefully lift the system and remove the three r ubber - c overed shipping blocks from underneath the system.
4. Carefully roll the system off the pallet using the ramp supplied with the system.
5. Attach the monitor to the system using the supplied hardware.

De-pallet the System (Series)

C-Arm

1. Remove the four metal brackets securing the wheels and C to the pallet.
2. Carefully lift the system and remove the three r ubber - c overed shipping blocks from underneath the system.
3. Carefully roll the system off the pallet . Be careful not to damage t he cable pushers.

Workstation

1. Remove the four turnbuckles.
2. Remove the four eyebolts from underneath the workst ation.
3. Carefully roll the workstation off of the pallet.
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Compact / Series 7600 Installation Procedure 11

Installation

As you perform the steps in this procedure check them off on the Installation Report/Checklist P/N 00-879038-02.
Additional information needed for operating the Compact / Series 7600 f ound in the Operator Guide’s.

Site Requirements

There are three major considerations for installing a system. They are:
1. Electr ical power requirements
2. Environmental condit ions
3. Safety precautions. The system requires an input power source capable of pr oviding nom inal
voltage inputs of:
115 VAC @ 15 Amps 230 VAC @ 8 Amps
The site must meet the line voltage regulation requirements as described in t he Installation Report/Checklist.
The customer is responsible for preparing the building, equipment , environm ent and services required to install and operate the system.

Installation Kit Contents

Verify that the following materials arrived in the 7600 Installation Kit (00-879040-01). Note any shortages on the Checklist.
Beam Film Labels
FDA Form 2579
FSP-10 Installation Paperwork Requirements SOP
Installation Procedure (This Document)
Installation Report/Checklist P/N 00-879038-03
Manual Response Form
Various Envelopes
Page 18

Cover Removal

C-Arm

Rear Cover
1.Unplug the system power cord from the AC power receptacle. Remove the two screws located on the lower front section of the rear cover
2. and the screw located on each side of the cover.
3
Move the cover toward the floor. (This will release the top tab restr aint s . )
.
Pull the cover away from the system
4
.
5. Remove the g r ound wire.

Workstation

Rear Cover
1. Remove the ten scr ews securing t he rear cover. Six along the sides and four around the power cord plate.
2. Pull the cover back away from the system.
3. Remove the g r ound wire.
Compact / Series 7600 Installation Procedure12
.

Mechanical Checks

In the steps below, check for ease of m ovement without excessive play.
1. Check t he system in place by pressing the locking pedals down completely (Compact / Series).
2. Check t he proper operation of the wig wag lock.
3. Check t he the cross arm lock.
4. Check the
Point
5. Check t he resistance to stop the C-Arm when the brake is applied.
6. Check t he
Locking Pedals
Wig Wag
Cross Arm
Flip Flop
. Check proper action of the pivot lock.
Radial Movement
Steering Handle
movement of the system from side to side. Verify
movement of the system. Verif y proper operation of
movement of the system and integrit y of the

Inspection and Setup

1. Verify or mount the skin spacer as directed by state regulation.
2. Inspect the AC power cable and interconnect cable for proper strain relief.
Inspect the power cable assembly and interconnect cable assembly for any shipping damage. Look f or any signs of damage or abrasion to the cable jacket and inspect each plug f or loose pins.
of the system for proper operation. Lock the
Pivot
of the system and verify there is adequate
of the C-Arm f or pr oper operation.
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Compact / Series 7600 Installation Procedure 13

Line Voltage Compatibility Check

Check the line voltage in each room where the equipment operates. Do not assume the line voltage will be constant throughout the hospital.
Verify voltage compatibility in all hospital room s where this machine will operate. If a particular r oom is unavailable, write " NK" in the location, voltage and plug compatibility blanks on the checklist . A room is not plug compatible when the plug requires an adapter. Notify the hospital if any rooms are not voltage compatible.

Isolation Transformer Wiring

1. The isolat ion transformer(s) of the Compact / Series 7600 reside in the lower left portion of the gener ator cabinet. And in the lower rear section of the workstation (Series).
2. Direct ly above the generator isolation transformer and in t he lower rear of the workstation is the isolation transformer terminal block. The isolation transformer(s) have input taps for 90, 100, 110, and 120V.
3. Unplug the system from the wall receptacle and measure the AC voltage at the wall receptacle. Move the brown wire on the isolation transformer terminal blocks to the appropriat e input tap.

Power ON System

1. Plug the AC power cord into the system and then the wall receptacle (Compact).
2. Connect the interconnect cable between the generator and the workstat ion (Series).
3. Plug the AC power cord into the wall receptacle (Series).
4. Tur n the system on by pressing the green START butt on on the control panel (Compact / Series) or workstation (Ser ies) .
5. The system will display the OEC test pat tern on the monitors when the system has initialized.
6. Verify that the elapsed time indicator operates on the generator.
NOTE
: The elapsed time indicator will increment every 6 minutes or 1/10th of an hour.
If the indicator is not running initiate repairs before continuing the installation.
7. Verify that the cooling fan operates (Series).
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Compact / Series 7600 Installation Procedure14
j
5
djustable
j
39+5

System Power Supply Voltages

1. The power supplies reside in a per forated metal enclosure on the lef t side of the generator cabinet. There are two separate power supplies (Compact) and one (Series) in the enclosure.
2. Locate the output voltage wire bundle coming from the top power supply (NG1). This wire bundle exits the enclosure on the left side and has a 15­pin connector on the end of the bundle. The 15- pin connect or designation is P1. Measure the voltages listed below and record them on the Installation Checklist.
GND To Ad
P1-2 P1­P1-2 P1-4 Not Adjustable +24V P1-2 P1-1 R39 +16V
3. Locate the output voltage wire bundle coming from the bott om power supply (NG2) (Compact). This wire bundle exits the enclosure on the lef t side and has a 9-pin connector on the end of the bundle. T he 9- pin connector designation is P2. Measure the voltages listed below and record them on the Installation Checklist.
GND To Ad
P2-2 P2-1 R P2-2 P2-4 Not Adjustable +12V P2-2 P2-5 Not Adjustable -12V
Not A
ust Voltage Tolerance
ust Voltage Tolerance

Measure Line Voltage Regulation

1. Measure the AC line voltage at t he wall recept acle.
NOTE
: In the next step the voltage measured at the wall receptacle will drop
immediately after the exposure terminat es. Read t he meter at this time.
+5V
±1V ±1V
V
±1V ±1V
2. Measure the line voltage at t he wall receptacle again while making a radiographic exposure (80 mAs @ 110 kVp).
3. Calculate t he per centage line voltage regulation using t he following formula and record the results on the Installation Report / Checklist.
100 X
Vn - Vl
where: Vn = No load voltage Vl = Max load voltage
Vl
4. If the results above do not fall within the range of 0 to 15 percent, inform the hospital that an in-house wiring problem exists. (This problem results in a violation of a provision of the Federal Performance Standards 21 CFR
1020.30)
Page 21
Compact / Series 7600 Installation Procedure 15

System Operational Verification

Generator

S
1. Press the
C-Up
kV
and
mA
C-Down
buttons and verify that the C-arm lifts
min s
PRINT
HIP
smoothly from the top to the bottom limits.
2. Press the
Auto Fluoro
button and verify that the LED illuminates. Press the x-ray button and verify that the kV automat ically servos by monitoring the kV display and that an image appears on the monitor. Verify that the mA display displays the mA value while x-rays are being taken.
3. Press the
Pulse Fluoro
the x-ray button and verify that the system produces pulsed x-rays and that an image appears on the monitor.
4. Press the
Snapshot
button and verify that the LED illuminates. Pr ess t he x-ray button and verify that an exposure initiates and then automat ically terminates. The image should r emain on the monitor until you take the next exposure.
button and verify that the LED illuminates. Pr ess
Page 22
Compact / Series 7600 Installation Procedure16
5. Press the
Manual Fluoro
button and then the
button and verify that the
kV
LED illuminates. Press the kV-up/down button and verify that t he kV can adjust from 40kV to 110kV.
6. Press the
Timer-up/down
button and verify that the LED illuminates. Pr ess t he
Film
button and verify that you can select a time from 0.1 sec. to 4 sec. as shown on the seconds display. Take a number of film shots at various kV and mAs settings to verify the film mode operation.
7. While taking x-rays in the Auto Fluoro mode press the
Slot Collimator
open and close buttons and verify that the collimator opens and closes.
8. While taking x-rays in the Auto Fluoro mode press the
Slot Collimator
rotate buttons and verify that the collimat or r otates in both directions.
Film
9. While taking x-rays in the Auto Fluoro mode press the
Iris Collimator
open and close buttons and verify that the iris opens and closes.
10. Press the
Magnification
button and verify that the LED illuminates. Verify the image on the monitor chang es t o the small field mode when x-rays initiate.
11. Press the
Image Reversal
button and verify that the LED illuminates.
Verify the image reveres horizontally when x-rays initiate.
12. Press the
Image Rotation
buttons and verify that the image on the m onit or rotates in both directions. Press both keys simultaneously and verify that the image rotates to the nor mal orientation and automatically stops.
Page 23
Compact / Series 7600 Installation Procedure 17
13. Place som e lead apr ons on t he image intensifier to att enuat e the beam. Press the
Thorax Surgery
button and verify that the LED illuminates.
14. Press the
Hand Surgery
button and verify that the LED illuminates. Take an x-ray and verify that the field size automatically decreases because the iris collimator closes partially.
15. Press the
Hip Surgery
button and verify that the LED illuminates. Take an
x-ray and verify that the mA increases to a maximum of 6mA.
16. O bt ain an im age on the monitor and press the
button. Verify that the
Save
image saves by noting the image storage number that will appear on the monitor.
17. Save 4 distinct im ages in memory using the Save button. Press the
Recall
button repeatedly and verify that the saved images display in
sequence on the monitor.
Image
18. Press the
Auto-Histo
button and verify that the LED illuminates. Ver ify that when the Auto-Histo is active the x-ray images are optimized for cont r ast and brightness automatically.
19. Press the
Low Dose
button and verify that the LED illuminates. Ver ify that
the technique reduces in comparison to a normal Auto Fluoro exposure.
20. Pr ess and hold t he
Alarm Reset
button for at least 2 seconds and verify
that the accumulated fluoro time shown on the display is cleared to zero.
21. Ver ify that x-rays initiate using the f oot switch.
Page 24

Workstation

ESC
1
Compact / Series 7600 Installation Procedure18
=
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432
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8
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POIUTREWQ
ALT
CTRL
SPACE
5360
L L
1. Press the
5851
62
W
63
52
Auto Windowing
MNBVCX
C
55
64
button 51/30 to turn on/off the auto windowing
LKJHGFDSA
>
-
:
.
#
6566
56
,
67
54
SPACE
68
Print
50
69
70
function. If you turn off the auto windowing you can activate the manual window function by pressing the
button 53 at the same time as the
Shift
auto windowing button. The letters ENH will appear on the monitor . Then press the
Adjust
buttons 52 to manually select the window and level
values.
L L
W
61
TEXT
5760
2. Press the settings.
3. Press the
51/30
Home
Lock
button 58 to return the window levels to the standard
button 17 to lock the kV value.
53
52
58
17
Page 25
Compact / Series 7600 Installation Procedure 19
4. Press the
5. Press the
Zoom
button 62 to digitally magnify the image four times.
62
Edge Enhancement
button 63 to sharpen edge definition. Once
you apply sharpen it remains. Sharpen will not toggle.
63
6. Press the
Image Negate
button 66 to reverse the display of light and dark values in an image. Press it a second time to retur n the image to the original display.
66
7. Press the
Image Collage
button 64 to minify the lef t m o nit or image to one­quarter size and display on the right monitor . Simultaneous display of up to four images is possible. Te xt will not display in the minified images.
64
8. Press the
button 55 to save the four image collage. Swap the
Save
collage to the left monit or button 65 before saving.
55
56
9. Press the
10. Press the
Recall
button 56 to preview the previously saved images.
Clear Image Display
65
button 67 to clear the left m onitor.
C
67
Page 26
Compact / Series 7600 Installation Procedure20
NOTE:
11. Press the
Exchange Image
button 65 to toggle the images between
monitors.
65
12. Press the
Shift
53and
57 buttons at the same time to enter pat ient
Text
data.
TEXT
13. Press the
Backspace
53
59, the
Space
57
60 and
Return
61 to manipulate the
patient data.
SPACE
59
60
61
The DSA, MSA and RSA buttons are not functional at t his time.

Thermal Printer / Multiformat Camera

1. Press the
Thermal Printer
thermal printer.
2. Inser t the film cassette and view the LED display to determine the number of available exposures 54 and press key 69 to expose the left monitor image.
button 68 to print the left monitor image to the
Print
68
54
69
Page 27
Compact / Series 7600 Installation Procedure 21

Fluoroscopic Image Tests

1.Select AUTO FLUORO mode. 2
rify that the kVp tracks up and down during X-rays as material thickness
.Ve
increase and decrease per the ranges below:
FILTERS kVp RANGE
1 Copper Filter 59-65 2 Copper Filters 70-76 3 Copper Filters 79-85
Remove the copper filters.
3
.
4
lace the Converging Lines Resolution Tool (00-900860-01) on t he image
.P
intensifier assembly. Select NORMAL field size, then MAG mode. Check image resolution in line-pairs-per millimeter (lp/mm) during live imaging (auto fluoro mode) f or each field size. Minimum acceptable resolution is:
Field Size 9” Image Intensifier
Normal 1.4 lp/mm
MAG 1.8 lp/mm

Radiographic Beam Alignment Test

Setup

1. Release the C- Ar m brake and position the C-Arm at a 45 deg r ee angle to nominalize the C-Arm flexure.
2. Att ach t he Beam Alignment Tool (00-878105) to the Image Intensifier .

Beam Alignment Verification

1. In ser t a film cassette into the Beam Alignment Tool.
2. Select
3. Select the X-Ray ON key for 2 seconds.
4. Select the
5. Collimat e t o t he m inim u m field size using the iris collimator close button and press the X-Ray ON key for 2 seconds.
MANUAL FLUORO
NORMAL
MAG
field size and set the technique to 50 kVp. Pr ess t he
mode and press the X-Ray ON key for 2 seconds.
mode.
Page 28
Compact / Series 7600 Installation Procedure22
6. Develop the film and visually check the film to determine whether the field sizes are within the following specifications:
FIELD SIZE RING
NORMAL A
MAG B
7. Verify that the minimum field size is less than 5 cm2.
8. Use a ruler and verify the center of the image appears on the sheet of film (in both the X and Y axis) within 20 mm or 13/16-inch.
9. If the films do not meet t he specification, refer t o t he Beam Alignment procedure in the Compact / Series 7600 Service Manual.

Complete Paper Work

1. Make sure that all portions of the Installation Report /Checklist are completed.
2. Make sure the beam alignment films are proper ly labeled.
3. Distr ibut e the copies of the FDA form 2579 t o t he appr opriate individuals as outlined on page 1.
4. Return the Inst allation Report/Checklist to OEC imm ediat ely.
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