Video Signal.............................................................................................................................................. 7
Tube Data And Rating Charts.....................................................................................................8
General Tube Data.................................................................................................................................... 8
X-ray Generator Information .......................................................................................................9
Unpacking and Inspection ......................................................................................... 10
Complete Paper Work...............................................................................................................22
Page 7
Compact / Series 7600 Installation Procedure1
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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 SMBOLPROTECTIVE EARTH STUD
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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.
Page 9
Compact / Series 7600 Installation Procedure3
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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.
Page 10
Compact / Series 7600 Installation Procedure4
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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 VAC30 milliamp current source
15 VAC30 milliamp current source
Page 11
Compact / Series 7600 Installation Procedure5
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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).
Page 12
Compact / Series 7600 Installation Procedure6
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X-ray Source Assembly
TypeFixed anode type
Focal SpotDual, 0.6 mm and 1.5 mm
Total Filtration>3 mm minimum aluminum eq uivalent
Anode Heat
Storage Capacity76,000 HU
Leakage
Technique Factors110 kVp and 3.0 mA
Voltage Rating110 kVp maximum
Fluoroscopy
Focal Spot Size0.6 mm
High Voltage Range 36 kVp to 110 kVp, with manual adjustment
available.
Current RangeStandard 3 mA maximum
Dense Anatomy 6 mA maximum continuous
Snapshot 8 mA
Duty Cycle:110 kVp @ 6 mA maximum continuous
CollimationNominal 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 Spot0.6 mm
kVp Range 36 kVp-110 kVp
mA Range0.2 - 8.0 mA
Pulse Rate1 pulse per second.
Page 13
Compact / Series 7600 Installation Procedure7
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Radiography
1.5mm Focal SpotHigh voltage range: 36 kVp t o 110 kVp
Tube current 20 mA fixed.
TimerDuration of radiography can be manually set
from 0.1sec to 4.0 sec with an internal electronic
timer.
Duty Cycle110 kVp @ 20 mA maximum for 4.0 seconds.
CollimationNominal 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 CassetteStandard: 10 x 12 x 5/8-inch nominal.
HolderMetric: 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
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
Extended0 to 40 degrees C
Storage and
Transportation
Short-term-10 to 55 degrees C
Storage and
Transportation
Page 14
StabilityPositive stability on grades up to 10 degrees when in
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transport position and on grades up to 8 degrees in any position
Altitude8,000 ft. (2438 meter s ) m aximum
HumidityOperating: 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.
Leakage110 kV at 3. 0 mA. This is also the maximum continuous
Techniquerating of the X- r ay tube housing assembly. 110 kV at 3.0
FactorsmA are the leakage technique factors used for the
diagnostic source assembly.
Total>3.0 mm minimum aluminum equivalent.
Filtration
Anode Heat76,000 HU
Storage
Anode330 HU/second maximum. Refer to the Thermal
MaximumCharacteristics curves in this section.
Cooling Rate
Page 15
Compact / Series 7600 Installation Procedure9
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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 Fluoro3 mA @ 110 kVp
Dense Anatomy Fluoro6 mA @ 110 kVp
Pulsed Fluoro3 mA @ 110 kVp
Snapshot Fluoro8 mA @ 110 kVp
Film Mode20 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 Mode2.2 kW @ 110 kVp, 20 mA
4.Nominal Output Power for 0. 1 Second Exposure
Film Mode2.0 kW @ 100 kVp, 20 mA
5.Reference mAs @ 50% of Nom inal O ut put Power
Film Mode2.0 mAs @ 55 kVp
(20 mA, 0.1 second)
6.(Not Applicable)
7.(Not Applicable)
8.Nominal Shortest Exposure Time
Film Mode0.1 second
Page 16
Compact / Series 7600 Installation Procedure10
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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.
Page 17
Compact / Series 7600 Installation Procedure11
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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
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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.
Page 19
Compact / Series 7600 Installation Procedure13
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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).
Page 20
Compact / Series 7600 Installation Procedure14
j
5
djustable
j
39+5
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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.
GNDToAd
P1-2P1P1-2P1-4Not Adjustable+24V
P1-2P1-1R39+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.
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 Procedure15
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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
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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 Procedure17
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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
Used and Refurbished C-Arms are Available from www.SharpMedical.com - Call us at 800-969-9800
An Independent C-Arm Service Provider. This PDF provided for research / historical purposes only.
ESC
1
Compact / Series 7600 Installation Procedure18
=
)
(
"
%
432
/
8
7
65
0
9
'
*
’
+
59
POIUTREWQ
ALT
CTRL
SPACE
5360
LL
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.
LL
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 Procedure19
Used and Refurbished C-Arms are Available from www.SharpMedical.com - Call us at 800-969-9800
An Independent C-Arm Service Provider. This PDF provided for research / historical purposes only.
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
Used and Refurbished C-Arms are Available from www.SharpMedical.com - Call us at 800-969-9800
An Independent C-Arm Service Provider. This PDF provided for research / historical purposes only.
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 Procedure21
Used and Refurbished C-Arms are Available from www.SharpMedical.com - Call us at 800-969-9800
An Independent C-Arm Service Provider. This PDF provided for research / historical purposes only.
Fluoroscopic Image Tests
1.Select AUTO FLUORO mode.
2
rify that the kVp tracks up and down during X-rays as material thickness
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 Size9” Image Intensifier
Normal1.4 lp/mm
MAG1.8 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
Used and Refurbished C-Arms are Available from www.SharpMedical.com - Call us at 800-969-9800
An Independent C-Arm Service Provider. This PDF provided for research / historical purposes only.
6.Develop the film and visually check the film to determine whether the field
sizes are within the following specifications:
FIELD SIZERING
NORMALA
MAGB
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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