During repairs/service interventions, observe the protective measures against
damage due to ESD.
·GE Medical Systems Information Technologies GmbH considers itself responsible
for the effects on safety, reliability, and performance of the equipment, only if:
-assembly operations, extensions, readjustments, modifications, or repairs are
carried out by GE Medical Systems Information Technologies GmbH or by
persons authorized by GE Medical Systems Information Technologies GmbH,
-the electrical installation of the relevant room complies with the applicable
national and local requirements, and
-the instrument is used in accordance with the instructions for use.
·This manual contains service information; operating instructions are provided in the
operator’s manual of the instrument.
·This manual is in conformity with the instrument at printing date.
·All rights are reserved for instruments, circuits, techniques, and names appearing in
the manual.
The authorized representative for GE Medical Systems Information Technologies Inc.
in Europe is:
GE Medical Systems Information Technologies GmbH
Munzinger Str. 5
79111 Freiburg, Germany
Tel. +49 (0) 7 61 45 43-0
Fax: +49 (0) 7 61 45 43-233
This document is subject to the GE Medical Systems Information Technologies change order system.
The revision code, a letter that follows the document part number, changes with every update of the manual.
There are 2 CardioServ models: the semi-automatic and the manual defibrillator. Both
models are available with a pacemaker and SpO2.
The manual CardioServ is a defibrillator designed to deliver synchronized and
unsynchronized shocks. This requires the user to trigger capacitor charging and shock
delivery manually.
The semi-automatic defibrillator is equipped with analysis software, which monitors the ECG
for arrhythmias (fibrillation and ventricular tachycardia). When the analysis is started by
pressing a key the ECG is analyzed. If the result of the analysis is positive, the capacitor is
charged to the preselected energy level. The semi-automatic operating mode can be
terminated by pressing a key or inserting the dongle.
2.1 Documentation and nomenclature of GE Medical Systems
Information Technologies instrument part Nos
2.1.1Configuration of instrument part No
The instrument part No comprises 8 digits, the first 6 digits determining the instrument
type, the last 2 digits the instrument version. The language is determined by configuration,
thus having no influence on the part No.
E.g. Instrument TypeVersion
CardioServ101117 ..
without pacemaker10111703
with SPO
with pacemaker and SPO
2
2
10111704
10111705
2.1.2Configuration of the PCB part Nos
388 xxx yySpare part numbers for the operative PCBs.
The instrument documentation, e.g., reference diagrams, circuit diagrams and parts lists
are listed under this part No.
The 388 number is located on the barcode label.
Configuration of the barcode labels:
Consecutive number
Consecutive number barcodeTest mark
0000000219
388 011 513131C3
Part No.Parts list index
Test number (batch)
Version 4.x CardioServ - 7 Revision J 227 483 02
General Introduction
303 xxx yySpare part numbers for PCBs tested especially thoroughly
303 numbers are only given to PCBs where the level of testing applied to 388 PCBs is
inadequate for implementation when servicing in the field, or where only a complete set of
PCBs can be replaced in the field.
In addition to a barcode label (388 number) 303 part Nos also have an additional label with
a 303 number and are to be found in the spare parts list under this number.
389 xxx yyReplacement numbers for defective PCBs
Where servicing is required 389 PCBs are available for the replacement of some PCBs.
When using a replacement PCB (389 part No) the defective PCB is to be returned to the
Freiburg factory. Replacement PCB part Nos are included in the spare parts list.
389 PCBs have an additional adhesive label.
2.1.3 Instrument status documentation (nominal status)
Due to the hardware and software combination unambiguous documentation of the instrument assembly status is necessary, also in the event of repairs.
This documentation comprises the following documents and measures:
Master Record Index (MRI) (see Appendix)
This document is a component of this instrument documentation.
This document states the combination of permissible hardware and software for a particular instrument version. The permissible PCB Index is given in the “Index” column with each
update delivered. Further permissible PCB Indexes are given in the “compatible” column.
The PCB Index can be found in the PCB barcode label.
Product Status Index
This document is created during manufacture. The Product Status Index documents the
hardware/software product status.
These servicing instructions describe the manual CardioServ and the semiautomatic CardioServ VF
Manual CardioServ
101 117 01 CardioServ without pacemaker, without SPO2
101 117 03 CardioServ with pacemaker, without SPO2
101 117 04 CardioServ without pacemaker, with SPO2
101 117 05 CardioServ with pacemaker, with SPO2
101 117 02 CardioServ Esaote without pacemaker, without SPO2
101 117 06 CardioServ Esaote with pacemaker, without SPO2
101 117 07 CardioServ Esaote without pacemaker, with SPO2
101 117 08 CardioServ Esaote with pacemaker, with SPO2
CardioServ VF
101 117 21 CardioServ without pacemaker, without SPO2
101 117 22 CardioServ with pacemaker, without SPO2
101 117 23 CardioServ without pacemaker, with SPO2
101 117 24 CardioServ with pacemaker, with SPO2
101 117 29 CardioServ Esaote without pacemaker, without SPO2
101 117 30 CardioServ Esaote with pacemaker, without SPO2
101 117 31 CardioServ Esaote without pacemaker, with SPO2
101 117 32 CardioServ Esaote with pacemaker, with SPO2
The Therapy System CardioServ comprises a defibrillator, a monitor ( LC display 240 * 320
pixels ), a printer and a power supply unit. These components are arranged in a casing. It is a
compact unit, which can also be implemented using a 230-V power supply system, even
without a battery. The unit has a pulsed 140-mA standard charge for the battery. Additional
versions available have an external pacemaker and an SpO2 module, separately or combined.
The Defi is switched on by turning the rotary switch to position ECG or energy levels automatic sequence 2 ... 360 J.
Following a self-test, which tests
- RAM data store
- ROM program memory
- Watchdog / Reset
- EEPROM permanent memory
- Display all Pixels on / off
- Time base of internal quartz crystal
- Energy charge from last shock
- Defective charge or Defib keys
- Position of energy selector switch
- Connected electrodes
- Pacemaker
- SpO2
the Defi is ready for operation. If an error arises, depending on the severity of the error, the
Defi is either on standby or not. Serious errors are watchdog, ROM or RAM errors. In the
case of minor errors, an error message appears, but the instrument can be rendered operative by pressing a key.
The Defi shock is delivered via exchangeable paddles. This permits the use of different
electrodes. In addition to conventional electrodes, large-surface adhesive electrodes or internal
electrodes, for example. Adhesive electrodes are used for the pacemaker. The CardioServ also
has Charge and Trigger buttons on the instrument.
The charge operation is actuated with the Charge key on the apex electrode (for internal and
adhesive electrodes on the instrument). During the charge operation, the accumulation of
energy is shown on the display. When the selected energy level has been reached, the energy to
be released appears on the display. An acoustic tone sequence and a message on the monitor
indicate that the selected energy level has been reached. When the battery is fully charged or
with line-power operation, charge time to 360 J should be about 8 s.
Version 4.x CardioServ - 11 Revision J 227 483 02
Functional Description
The buttons on both electrodes are pressed to trigger the defibrillation pulse (safety two-hand
operation). This means that the button on the apex electrode (or the corresponding one on
the instrument) has two functions:
- start the charge operation
- trigger defibrillation (together with the Trigger button)
The type of electrodes connected are identified and, in the case of internal electrodes, the
energy is automatically limited to 50 joules.
Following defibrillation, the energy released is displayed on the screen for 6 seconds. Documentation output is by the printer.
Cardioversion (operating mode Sync) can proceed either via the paddles or a patient cable.
The operating mode Sync appears on the display and Sync marks are superimposed on the
display. Following cardioversion, for safety reasons, the CardioServ switches automatically back
to the unsynchronized operating mode. Before each cardioversion the instrument must be
switched over to Sync mode.
The Defi can be configured for semi-automatic operation in three ways:
*As a semi-automatic instrument only (defibrillation only possible via analysis)
*Semi-automatic instrument which can be toggled to manual mode by pressing a key
*Semi-automatic instrument which can be reset into manual mode using a dongle
ECG signal pick-up is possible via the paddles or ECG cable. ECG is output on the LCD
display or by the built-in 50-mm printer.
A safety device ensures the discharge of the storage capacitor in the following situations:
-when defibrillation is not triggered 30 seconds after storage operation is complete,
-0.2 seconds after triggering defibrillation,
-immediately after switching back the energy selector switch during or after storage,
-when the battery voltage drops below a certain level,
-when the selected energy level still has not been reached after 32 seconds.
When switching to a higher energy level, the energy deficit is supplied by recharging.
The pacemaker is a transthoracic pacemaker operating in the Demand and Fix mode.
- Pulse width 40ms (20 ms)
- The frequency is between 0...180 P/min (> 150 P/min only 20ms pulse width)
- The current is between 0...200 mA
- Adjustment is in 5-unit intervals.
The pacemaker is operated using 6 keys on the control panel. One key switches the pacemaker on, one key changes the operating mode, the other keys are used to adjust the frequency and current. The defibrillator cannot be disabled as long as the pacemaker is
switched on. The adhesive electrodes of the Defi are used to release a pulse. This ensures a
rapid switch from defibrillator to pacemaker and back again.
SpO
2
SpO2 is based on a module manufactured by Nellcor. This module is located on the PCB Analog
and receives its power from the latter. Measurement of the oxygen saturation level and pulse
frequency is made by this PCB.
Pulse frequency from 0...250 P/min
Saturation from 0...100%
We display the plethysmogram, saturation level and, when selected, the pulse frequency
instead of the HR.
Control options:
A battery charge check is performed under load application. The message “charge battery”
on the display means the battery needs recharging. At least five discharges at maximum
energy are still possible. (Possibly even considerably more)
Performance check of defibrillation is performed by discharging into the integrated 50-Ohm
resistor.
Battery charge via the power cord connector can be monitored by the yellow LED. If the battery
is fully charged after 16 h, trickle charging ensues, the yellow LED is permanently lit up.
The monitoring function of the CardioServ records and monitors the ECG and oxygen saturation level. The cardiac-action potentials are fed to the ECG preamplifier via a 5-wire patient
cable. Selection can be made from 12 leads. The ECG curve is displayed on the LC screen
with an illuminated background. The heart rate obtained from the ECG signal is continuously
displayed on the screen.
Communication between the user and the instrument occurs via the keyboard and the LC
screen. These also serve to configure the default settings and functions (see User’s Manual for
further details).
Version 4.x CardioServ - 13 Revision J 227 483 02
Functional Description
The PCBs have the following functions:
PCB Power Supply
This PCB supplies the 16.5-V instrument power supply. 10 A can be supplied for short-term
capacitor charging. It is a primary clock-rated wide-range power supply system. It operates
from 95 .. 240 V, at 49 ... 65 Hz. It is protected by 2 fuses in the primary circuit.
PCB Analog
This PCB has several functional units.
The first unit accepts the ECG signals (patient input) received via the patient cable from the
patient. In accordance with its task, it is connected to the patient by a cable. It is thus
constructed as an application component isolated from other circuit components and the
circuit reference (floating). The tasks of this circuit component are:
- amplification of ECG signals
- lead selection (lead selector)
- identification and reporting of electrode defects
- identification and reporting of patient lead connection
- digitization and serialization of ECG data
- potential separation of the application component from the remaining circuit components
(floating)
- floating component power supply
- ECG trigger
- pacing-pulse detection
There are two of these circuit components on this PCB. Once for the ECG via paddles, once
for the ECG via patient cable.
A second unit provides floating separation and the power supply for SPO2.
A further circuit component controls high-voltage generation for the Defi shock. There is a
high-voltage capacitor on this PCB.
The functions are as follows :
- safety control during charging and shock release (1st path : hardware)
- controlling storage operation and energy release, independent of the CPU
- controlling the high-voltage generator
- elimination of interference in the operating elements in the Defi electrodes
- conversion of the voltage and current signals into a frequency to measure energy
- activation and control of the high-voltage transformer
- generation of the emergency cutoff signal in the event of inadmissibly high voltage
- measurement of the high voltage on the primary winding of the high-voltage transformer
- discharging the storage capacitor as a safety precaution
- measurement of the high voltage on the storage capacitor
- energy delivery via the high-voltage relay
A further unit organizes the entire instr ument´s power supply. This is provided by the built-in
battery, the power supply unit or, optionally, from an external battery (e.g., ambulance power
supply system). It has the following tasks:
- switching instrument on/off
- automatic cutoff when battery voltage is too low
- monitoring the “charge battery” threshold
- power source selection: battery or power supply system
- charging the built-in battery by a special circuit independent of how high the supply
voltage is
PCB Digital
The PCB Digital is equipped with the microcontroller, which controls the entire instrument. It
comprises a Motorola 68332 microcontroller, RAM, EPROM, EEPROM, watchdog and I/O
ports. It has the following functions:
- safety control during charging and shock release (2nd path : software)
- displaying the ECG and text on the LC screen (delete bar procedure)
- processing the curves and texts for the printer controller for output onto paper
- 50 / 60-Hz filter (software)
- alarm management
Circuit component display :
- graphics controller to control the display, which ensures screen refresh
- display RAM
- generation of voltages for the LCD ( LCD power supply )
- generation of high voltage for background illumination
- Pal for chip select generation for display
- contrast adjustment
Circuit component real-time clock :
- real-time clock with lithium battery buffer and integrated quartz cr ystal
- Pal for chip select generation for clock
Circuit component 1-channel recorder :
- single-chip microcontroller to output data at thermal-array printhead
- monitoring printhead temperature
- motor control for paper transport
- switches off motor in the event of overload or underload
Version 4.x CardioServ - 15 Revision J 227 483 02
Functional Description
- generation of power supply voltages for the recorder
- processing of all signals for the printer microcontroller
Further circuit components on the PCB are :
- generation of 5 V from 12 V via an integrated switching controller, short-circuit-proof and
protected against overvoltage by Transzorb diodes
- sound generator, frequency controlled by SW
- RS-232 interface, protected against overvoltage by Transzorb diodes. Interface integrated
into microcontroller, external conversion of level from 5 V to +- 12 V.
- energy selector switch, binary coded, delivers its information to PCB Analog and to the
microcontroller
- keyboard interface to connect the membrane keypad
- control of LEDs on the keypad
- watchdog
- reset generation, when +5-V supply drops below 4,65 V or exceeds 5,5 V
- RAM buffering by battery when instrument is switched off
- pacemaker functions integrated on PCB Digital
- serial hookup of pacemaker and microcontroller
- pacemaker conducts current when in operative mode only.
When CardioServ PCBs are replaced the technician must call up the self-test screen after
replacing the PCB. The new components are reported automatically in the software configuration. After restarting CardioServ recognizes the new components. This is important in the case
of SpO2 and Pacemaker. Further the Performance Check (see section 10.4) needs to be
accomplished.
Replacing PCB Digital
The identification numbers 0000 and 1111 are stored in the Eeprom of the PCB Digital for
CardioServ Manual and CardioServ VF, respectively.
The replacement PCB always has the identification number 0000 stored in the Eeprom for
CardioServ Manual.
If during servicing the replacement PCB Digital is inserted into a CardioServ VF, when it is
switched on the CardioServ is in the manual mode. The following combinations of keys are
required to switch the CardioServ from manual to semi-automatic operation.
1. Press F1 and F5 keys simultaneously: The function Configuration appears on the screen.
2. Press F3 and F4 keys simultaneously: The function Key Test appears on the screen.
3. Press the Analysis key.
4. Press F3 and F4 keys simultaneously.
The identification code for the CardioServ VF stored in the Eeprom of the PCB Digital is now
1111 and the CardioServ operates in the semi-automatic mode.
Version 4.x CardioServ - 19 Revision J 227 483 02
Before opening the CardioServ switch the instrument off, disconnect power cord plug, remove battery and implement ESD protection measures. Return replacement PCB in ESD
packaging only.
Opening the instrument:
Undo the 9 screws on the bottom of the device, place upper case shell to the left next to the
instrument.
Removing the PCB Digital:
The PCB Digital is located in the upper shell. Disconnect the 50-pin flat strip cable and the 2pin 12-V power supply cord. The recorder, plugged into the lower case shell, can be removed
and the flat strip cable connected to the thermal-array printhead and motor disconnected.
Lay the upper shell “face down”, remove the screening plate fixed in place by a screw and 5
plastic catches. Remove the insulating card. Undo the 8 PCB Digital fastening screws (leave
the 4 display screws in place) and remove the rotating knob of the energy selector switch.
Carefully lift up the PCB and pull out the membrane keypad connector on the left. The PCB
Digital can now be removed along with the display screen.
Removing the display screen:
-Disconnect plug-in connector to display illumination.
-Carefully pull the zero power connector safety catch of the display-membrane keypad
connector upwards and disconnect membrane keypad lead.
-Remove the 4 display fastening screws.
Removing the PCB Analog:
Disconnect 50-pin flat strip cable, connection cable to the battery, power supply unit and
PCB Digital. Detach connector to the ECG socket and disconnect connections to Defi socket.
Remove ECG amplifier cover with 3 screws and 2 plastic catches. Unscrew the 10 screws on
the PCB Analog (4 capacitors, 2 high-voltage oscillators) and 3 hexagonal columns.
Version 4.x CardioServ - 33 Revision J 227 483 02
•Fold the print head ribbon cable into the gap between the recorder and the lower housing shell before
drop the upper housing shell. This prevents that the upper housing shell drags the print head cable down
together with the print head. If this is ignored a bad print out can be occur.
Version 4.x CardioServ - 37 Revision J 227 483 02
Assembly Instructions
For final test please start a print out and verify the correctness. The test has to be done after the
CardioServ’s upper and lower housing shell is closed and screwed together.
If the print head ribbon cable is not accurate mounted parts of the print out are not or not accurate
printed.
If the ribbon cable is accurate mounted the print intensity is good and homogeneous.
-Fuse SI500 (16V) , SI501(background illumination) , SI502 (5V) on PCB Digital OK ?
-Display defective ?
-PCB Digital defective ?
No ECG on display via ECG cable or paddles
-Connector to ECG socket OK ?
-Connector to paddles OK ?
-Lead PCB Analog -- PCB Digital (50-pin control ) OK ?
-ECG via paddles or ECG cable OK : --> PCB Analog defective
-PCB Analog or PCB Digital defective ?
Battery does not charge:
-Yellow LED must glow when battery is being charged
-Fuse SI501 on PCB Analog defective ?
-Check connector to battery
-Voltage on power supply unit under 16 V
Self-test:
F1 + F5 simultaneously to go to configuration and with Print print out the current error
messages.
In configuration with F3 + F4 key test and carry out printer adjustment (Print key).
In configuration with F3 + F5 restore default (factory setting).
Display test chessboard pattern at power up.
Error in time base : The clock must be set once or PCB Digital defective.
Error in energy storage : Adjust energy storage / measurement or PCB Analog defective.
Error RAM, ROM, Display-RAM, permanent memory, watchdog : PCB Digital defective.
Error Charge or Discharge actuated (key sticking).
Troubleshooting hints for PCB SPO2
When the PCB SPO2 is inoperative or operates defectively check the 5V floating voltage.
The voltage must lie between 4.8-4.9V.
Version 4.x CardioServ - 41 Revision J 227 483 02
Troubleshooting Hints
7.1 Error Codes in the CardioServ Self-Test Screen
These errors can occur in combination : RAM + ROM : 0012
SpO2
No. 0“No”a),internal, no error
No. 1“RAM”b),MP204, RAM error
No. 2“ROM”b),MP204, ROM error
No. 3“Data Link”c),MP204, serial communication to SpO2 module is defective
No. 4“Command”c),MP204, defective commands from CardioServ to SpO2
module
No. 5“Value”c),MP204, defective values from CardioServ to SpO2 module
No. 6“Calibration”e),MP204, calibration error
No. 7“Not used”e),MP204, SpO2 is in calibration mode
No. 8“Calibr. request”c),MP204, calibration request rejected by SpO2 module
No. 9“Communication”c),MP204, defective commands from CardioServ to SpO2
module
No. 10 “Over-current”d), MP204, excessive sensor current identified
No. 11 “Post Aver Time”e),internal, Post Average Time (integration time setting not
adopted)
No. 12 “Post Aver Time”e),internal, Post Average Time (integration time scanning rate
not adopted)
No. 13 “Defect”e),internal, undefined error
a) no error, everything O.K.
b) SpO2 module no longer functions, replace SpO2 module
c) check connection from main board to the SpO2 module
d) replace sensor or cable and switch CardioServ off and then on again
e) switch CardioServ off and then on again
- 42 - CardioServ Version 4.x
227 483 02 Revision J
For your notes
Troubleshooting Hints
Version 4.x CardioServ - 43 Revision J 227 483 02
Adjustment Instructions
8. Adjustment Instructions
1
MP3/
R 504
R 505
R 506
R 507
AE/
34
MP1/
MP2/
AC/
1
1
AD/
1
AM/
6
1
AJ/
40
10
AK/
1
AG/
1
1AH/16
SI502
1
40
AB/
SI500
SI502
11
AI/
AA/
PCB Digital388 032 06
PCB Digital388 032 53
- 44 - CardioServ Version 4.x
227 483 02 Revision J
Adjustment Instructions
Motor Adjustment on PCB Digital
What to adjust or to What to measureHow to activateWhere to turn?How much andWhat else to note?
check?with?testing mode?exact?
Adjust motor speedFlash at motor pinion 1) Call up configura- Speed selectorStroboscopeMotor should be at
under small loadwith stroboscopetion (Press F1 + F5R 506frequencyroom temperature.
(recorder flap open) (LED).simultaneously)= 181.07 HzThe testing mode
on stationary motor2) Call up key testterminates automatipinion.(Press F3+F4 keysWhen a square wave cally after a few
Adjust motor speedCompensationIf the RPM changes
under normal loadadjusterafter compensation
(recorder flap closed)R 505adjustment, this
and small loadshould be corrected
(recorder flap open)once more only
so that there is nowith R521.
difference in RPM.
simultaneously)generator activatedseconds. This can be
3) Press Print keyby LED is used, asuppressed by
Speed selectorlow key ratio shouldpressing any key.
be observed.
Version 4.x CardioServ - 45 Revision J 227 483 02
No Stroboscope Available: Motor Adjustment on PCB Digital
What to adjust or toWhat to measureHow to activateWhere to turn?How much andWhat else to note?
check?with?testing mode?exact?
Adjust motor
speed under
small load (recorder
flap open wide
enough so that
paper is just
transported)
Adjust motor speed
under normal load
(recorder flap
closed)
Remeasure grid
printout.
min. 200 mm
1) Call up configuration (Press F1 + F5
simultaneously)
2) Call up key test
(Press F3+F4 keys
simultaneously)
3) Press Print key
Speed selector
R506
Compensation
adjuster
R505
< 1%
Motor should be at
room temperature.
The testing mode
terminates automatically after a few
seconds. This can
be suppressed by
pressing any key.
The adjust-procedure
is complete when
the RPM is 25 mm/s
under small load and
normal load.
Heating Time Adjustment on PCB Digital
Note:There exists two versions of printhead. The old one have no inscription, the new one have the
inscription R 650.
What to adjustWhat to measureHow to activateWhere to turn?How much andWhat else to note?printhead
or to check?with?testing mode?and exact?legend
Heating time
Connect oscilloscope
to MP2/1 and
MP1/1 (GND)
Press Print key
in main menu
Heating time
adjuster
R507
referred to 22°C
printhead
temperature:
500 μs ±1 %(blanc)
590 μs ±1 %
Adjustment ensues at
25 mm/s.
Important: printhead
warms up during
printing
R 650
5-V Overvoltage Cutoff Threshold on PCB Digital
What to adjust or toWhat to measureHow to activateWhere to turn?How much andWhat else to note?
check?with?testing mode?exact?
5-V power supply
monitoring
V oltmeter. Input
impedance >=
1MOhm
Between MP3/1
and GND
R504 2,720V <1%
- 46 - CardioServ Version 4.x
227 483 02 Revision J
Control of the Power Supply Voltages on PCB Digital
What to adjust or toWhat to measureWhere toHow muchWhat else to note?
check?with?measure?and exact?
5-V power supply
+22-V power supply
-23-V power supplyV oltmeter .
V oltmeter.
V oltmeter.
Between +5V
and GND
Between +22V
and GND (C504)
between -23V
and GND
5,0V +/-2%
+22V +/-5%Recorder stationary
-23V +/-5%
Version 4.x CardioServ - 47 Revision J 227 483 02
Replace PCB Analog if energy adjustment is not correct. FRU boards are completely adjusted
and must not be readjusted.
Energy adjustments must only be made at the f actory .
EC Amplifier Adjustment on PCB Analog
What to adjust or to What to measureHow to activateWhere to turn?How much andWhat else to note?
check?with?testing mode?exact?
Offset EC amplifier
cable
Amplification EC
amplifier cable
Offset EC amplifier
paddles
Amplification EC
amplifier paddles
Optical scale
Optical scale
Optical scale
Optical scale
Display
Printer
Display
Printer
R501
R500
R524
R522
Baseline offset
< 1 mm
10 mm
+-0.5 mm
Baseline offset
< 1 mm
10 mm
+- 0.5 mm
Connect ECG pickup
with paddles
Amplitude 1 mV
Toggle amplification
between 0.5, 1 and 2
ECG pickup 1 mV
Toggle amplification between
0.5, 1 and 2
Version 4.x CardioServ - 49 Revision J 227 483 02
adjustable, energy to be delivered into 50 ohms displayed digitally
*selectable energy levels, energy to be delivered into a 50-ohm resistance (max. energy of
*possible deviation from selected energy below values specified by IEC
Energy storage
by means of capacitor, capacitor is charged from battery, from a 12-volt power source (emergency vehicle) or from the power line (95 to 240 V; 49 to 65 Hz); when capacitor charging is
terminated buzzer sounds:
*capacitor charging time for energy setting of 360 J:
–from power line: typically 8 s
–from fully charged battery: typically 8 s
–from partially discharged battery: typically 10 s (15 s max.),
measured at least 5 minutes after 15 shocks of 360 joules each
(for 200 joules typically 4 s)
- 50 - CardioServ Version 4.x
227 483 02 Revision J
Technical Specifications CardioServ/CardioServ VF
Defibrillation shock
capacitor discharge via induction coil (damped serial resonant circuit), pulse shape = a sinusoidal halfwave with decay period:
*pulse duration for an external resistance of 50 ohms approx. 4 ms, measured from the
beginning of the pulse to the intersection of the zero line and the inflection point of the
trailing pulse edge
*in synchronized mode the defibrillation shock is released within 30 ms of the R-wave
trigger
Discharge circuit
serial oscillating circuit in series with external resistance (patient):
*capacitance 35 μF
*inductance 26 mH
*equivalent resistance 7.35 Ohm
Pulse output
isolated, no conductive connection with enclosure, open-circuit and short-circuit-proof
*isolation test voltage 8 kV DC, type CF according to IEC requirements
Safety discharge
capacitor discharge via internal load resistance:
*when the defibrillation shock is not triggered within 30 s after charging
*when the defibrillation shock is triggered, but the discharge circuit is interrupted, after
approx. 0.2 s
*immediately when reducing the selected energy during or after charging
*when the selected energy is not reached, after 32 s
*in the event of technical malfunctions
Test features
*pilot lamp for battery charging
*defibrillator test by discharging the stored energy into the internal 50-ohm load resistance;
3-digit display of the delivered energy
*warning on LCD when discharge circuit is interrupted (e.g., defibrillation paddle not ap-
plied)
*automatic defibrillator test on power up with display of error message, if applicable
Synchronization
with ECG signal of either polarity:
*min. ECG amplitude for reliable triggering approx. 0.5 mV with QRS duration of 80 ms
Version 4.x CardioServ - 51 Revision J 227 483 02
Technical Specifications CardioServ/CardioServ VF
ECG signal input via paddles
ECG signal acquisition via defibrillator paddles, ECG trace displayed on LCD, automatic
switching to ECG electrodes when patient cable is connected; cardioversion both via ECG
patient cable and via paddles; differential input; isolated, class CF according to IEC, with
overvoltage protection
*input voltage range ±4 mV
*input impedance >1.5 Mohm
*max. polarization voltage ±1V
*frequency response optimized for best standard ECG representation
*common-mode rejection >80 dB
*patient leakage current: in normal condition <10 μA, in single-fault condition <50 μA
*detection of pacing pulses
–pulse duration dp >approx. 0.1 ms <2.0 ms
–pace marker independent of polarity
–pulse amplitude ap ±20 to ±700 mV
–reverse-current pulse a0 ±1 mV
–time constant t0 = 25 to 100 ms
ECG signal input via patient cable
via ECG electrodes, automatic switching to ECG electrodes when patient cable is connected;
cardioversion both via ECG electrodes and via paddles; differential input, symmetrically
referred to N, isolated, class CF according to IEC; 7 standard leads selectable via lead selector; input with overvoltage protection (defibrillation-proof):
*input voltage range±4.4 mV for recorder,
±4 mV for display
*input impedance >2.5 Mohm for 10 Hz
*common-mode dynamic range ±3 V
*differential DC voltage compatibility ±1 V
*common-mode rejection (CMRR) R,L referred to N 65 dB, N referred to chassis >110 dB
*QRS trigger (measured according to AAMI EC 13): trigger threshold 0.3 mV (for QRS
widths between 40 ms and 70 ms and between 30 and 250 BPM)
*bandwidth .5 to 60 Hz
*patient leakage current: in normal condition <10 μA, in single-fault condition <50 μA
*ground leakage current: in normal condition .5 mA, in single-fault condition 1 mA
*voltage resistance referred to circuit reference 4 kV
- 52 - CardioServ Version 4.x
227 483 02 Revision J
Technical Specifications CardioServ/CardioServ VF
*detection of pacing pulses
–pulse duration dp >approx. 0.1 ms <2.0 ms
–pace marker independent of polarity
–pulse amplitude ap ±20 to ±700 mV
–reverse-current pulse a0 ±1 mV
–time constant t0 = 25 to 100 ms
Signal display
backlit LCD, 2-channel erase bar mode, calibration pulse in left-hand corner (for ECG)
alphanumeric presentation of alarm messages, sensitivity, leads, systole blinker, alarm
limits, heart rate, energy and softkey labels
ECG freeze with simultaneous display of the current ECG and (for units with SpO
2
function) plethysmogram at a smaller scale
ECG trace 1.5 times larger than on recording: with a sensitivity of 1 cm/mV a 1-mV
signal has an amplitude of 1.5 cm on the display
*erase bar sweep speed 25 mm/s
*trace length in real-time mode 4.6 s
*display dimensions: 115 mm wide, 86 mm high
*resolution 320 x 240 pixels (pitch of .36 x .36 mm)
*displayed image can be rotated 180°
Signal transmission
signal input —> amplification —> signal sampling —> AD conversion —> digital
processing —> LCD and recorder
*selectable sensitivity: .5-1-2 cm/mV (with max. sensitivity of 2 cm/mV a 1-mV input
signal is 2 cm in amplitude on the recorder and about 3 cm on the LCD), amplitude
limited to approx. ±2 cm on the recorder and approx. ±3 cm on the LCD
*signal sampling rate 1000 Hz at mains frequency of 50 Hz, 1200 Hz at mains fre-
quency of 60 Hz
ECG signal output (“Option” port)
*ECG lead shown on display
*1 V output signal for 1 mV input signal (at 1 cm/mV)
*U
max
±2 V
*overall error < 3% (typical)
*RL 500 Ohm min.
*delay < 150 ms (not suitable for precise triggering)
9 = ECG
10 = chassis
Version 4.x CardioServ - 53 Revision J 227 483 02
Technical Specifications CardioServ/CardioServ VF
Systole check
*heart symbol flashing on the LCD
*QRS beep (can be disabled)
*AC line filter 50 Hz (60 Hz); interference elimination
*muscle filter
low pass filter withf
f
= 27 Hz (50 Hz mains)
lim
= 32 Hz (60 Hz mains)
lim
cut-off at 83/100 Hz
Heart-rate measurement
derivation of trigger pulses from the ECG of either polarity, adaptive trigger threshold, calculation of the average rate, storage of the result, 3-digit display on LCD, alarm limits to the left of
the reading:
*measuring range 15 to 300 BPM
*digit height of HR reading 7.5 mm
*digit height of alarm limits 2.5 mm
*min. amplitude for reliable triggering >.25 mV for ECG signal with a QRS duration of 80
ms
Alarm system
electronic release of alarm
*when the HR violates one of the set limits for at least 5 s: alarm tone sounds (can be
disabled), message “Alarm, high HR” or “Alarm, low HR”, recorder starts (if configured)
*when at least one of the selected electrodes drops off: audible signal (if patient cable is
plugged in), message “Alarm, Electrode” on display
*alarm limits adjustment range 15 to 300 BPM (not overlapping)
*digit height of alarm limits 2.5 mm
*keys to cancel alarm and to silence alarm tone
*softkeys to adjust alarm limits
*when set up for VF detection running in the background, alarm release can be enabled or
disabled
- 54 - CardioServ Version 4.x
227 483 02 Revision J
Technical Specifications CardioServ/CardioServ VF
Recording
delayed recording of the ECG stored in the signal memory (strip length 16 s, incl. 4-s history)
in the event of an alarm plus alphanumeric annotations on the paper margin:
–heart rate
–lead
–filter
–date
–time
–paper speed
–cause of recording (defib, alarm, manual)
–selected energy
–delivered energy
–sync mark
–text (name of user/hospital/practice)
After the ECG recording, a patient ID sheet is printed indicating name, date of birth, user,
comments, date, time, energy and alarm limits.
Direct writing with rectangular coordinates using thermorecording technology (printhead with
electronically controlled thermal elements records on thermosensitive paper), baseline fixed
at the center of the space available for recording of the ECG trace, grid imprint, roll paper,
paper transport by electronically controlled DC motor, limited duration of transport
*number of recording channels 2
*paper width 55 mm
*roll diameter 60 mm max. (roll with 40 m of GE Medical Systems Information
Technologies CONTRAST®)
*printhead resolution vertical 6 dots/mm, horizontal 24 dots/mm
*paper speed 25 mm/s ±5%
*paper transport after both manual and automatic start 16 s (incl. history of 4 s after automatic
recorder start)
To prevent damage to the printhead, use only the original GE Medical Systems InformationTechnologies CONTRAST® chart paper.
Memory
*storage of 40 ECG strips initiated by defibrillation or alarm with a length of 16 seconds
and a history of 4 seconds each, incl. a full report
*storage of the 80 most recent actions (e.g., power on, power off, alarms, defibrillation
energy) incl. date and time
Version 4.x CardioServ - 55 Revision J 227 483 02
Technical Specifications CardioServ/CardioServ VF
SpO
2
*saturation: 0 to 100 %, in 1-% increments
*frequency: 0 to 250 BPM, in 1-BPM increments
*alarm limit: off, 15 to 100 %
*display of plethysmogram
*C-LOCK ECG synchronization
*integration time: 4, 8 and 12 seconds
*measuring accuracy:70 to 100% ±2 digits
50 to 69% ±3 digits
pulse display 1.2% or ±1 BPM
Pacemaker
*operating modes:demand, fixed-rate
*pacing rate:30 to 180 BPM
*pacing current:0 to 200 mA (for 500 Ohms),
voltage up to 120 V
*pulse width:40 ms
20 ms (for pacing rate of 155 BPM and higher)
*pulse shape: monophase square-wave pulse
*error message “Check Electrode” when pacer output differs from set value (±20% or
±20 mA)
Power
from the power line
*95 V to 240 V, 49 Hz to 65 Hz
*power consumption at 230 V
– during monitoring 160 mA
– during capacitor charging 750 mA
*from a 12-Volt power source of the emergency vehicle
*from exchangeable, rechargeable NiCd batteries
*rated voltage 12 V
*rated capacity 1.4 Ah
*battery is charged while inserted in the unit
*charging time for depleted battery approx. 16 hours
- 56 - CardioServ Version 4.x
227 483 02 Revision J
Technical Specifications CardioServ/CardioServ VF
*operating time with a fully charged battery approx. 35 defibrillation shocks of 360 joules
each (into 50 ohms) or 2 hours of monitor operation (1.2 hours with pacemaker and SpO
measuring system)
Operational readiness
4 s after power up (incl. automatic selftest)
Operating position
any
Environment
Operation
under the following conditions regarded as normal:
*temperature between 0 and +40 °C
*rel. humidity between 30 and 95%, no condensation
*atmospheric pressure between 700 and 1060 hPa
2
Storage and transport
*temperature between -20 and +60 °C
*rel. humidity between 10 and 95%, no condensation
*atmospheric pressure between 500 and 1060 hPa
Dimensions
*width 432 mm
*height 172 mm
*depth 377 mm
Weight
*approx. 8 kg (incl. battery)
Version 4.x CardioServ - 57 Revision J 227 483 02
Maintenance and Technical Inspection
10. Maintenance and Technical Inspection
Technical Inspections
Testing the operating and functional safety of the CardioServ is carried out according to the
checklists below.
They serve the experienced technician when inspecting the instrument. A knowledge of how
to operate the CardioServ in compliance with the operator’s manual is assumed.
The tests are based on the calibration devices described below. Where possible, the tests
should be conducted using the customer’s accessories to also detect any defective accessories automatically.
Using calibration devices other than those named below may require changes in the tests
and tolerance specifications.
10.1 General Information
The CardioServ is an instrument with an internal power source assigned to Protection Class I
and Class IIb ( MPG ).
The instrument is suitable for external and internal defibrillation (as well as cardioversion).
The heart rate is monitored with configurable alarm limits. Upgrade options include a transcutaneous pacemaker and / or SPO2 calibration module; the latter can also be monitored.
In addition, the CardioServ VF has the following operating modes:
-manual
-semi-automatic with the option to switch over to “manual” by pressing a key
-semi-automatic with the option to switch over to “manual” with the help of an encoding
module
-as a semi-automatic instrument
Caution!
CardioServ uses high voltage. The inspection should be referred to independent persons with adequate training and experience.
These inspections must be carried at least once a year.
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227 483 02 Revision J
Maintenance and Technical Inspection
10.2 Testing Equipment
ECG simulator
Defib tester with pacemaker test functionality, e.g., Fluke 7000DP
Safety tester, e.g., NSE
1X SPO2 simulator, e.g., NELLCOR SCR-MAX
1X Finger probe701 240 21
1X Trunk cable for SpO2 sensor303 443 58 used up to S/N 101157661
1X Trunk cable for SpO2 sensor2026751-001 used from S/N 101157662
Dongle (optional for CardioServ VF)303 445 15
Version 4.x CardioServ - 59 Revision J 227 483 02
Maintenance and Technical Inspection
Recommended Test Equipment
-Safety Tester for measurements according to IEC 601.
-Testing connector according to the following drawings.
Testing connector for measuring patient leakage current
The following wiring of testing connectors is recommended for the technical inspection of
module input type BF (body floating) and type CF (cardiac floating).
The catalog numbers of the GE Medical Systems Information Technologies components
are given below.
When making the connectors observe the following configurations:
The diagrams of the plug inserts in this document are always as viewed from the inside of
the connector shell.
-Testing connector for the temperature input
1 x2-pin jack plug91530000
1 xTelephone socket or91534800
matching isolated plug connection for testing case
The two jack plug poles are short-circuited with one another and connected to the
matching isolated plug connection for testing case
6*10 kohm resistor92184443
Connect pin 10 directly to the telephone socket.
Connect pins 1,4,5,6,7,9 via 10 kohm resistor to telephone socket.
- 60 - CardioServ Version 4.x
227 483 02 Revision J
Maintenance and Technical Inspection
Measure patient leakage current on the Defi electrodes
The patient leakage current on the Defi electrodes is measured directly on each paddle.
10.3 Visual Check
Test instrument and accessories to ensure that
-fuse links have the rating proclaimed by the manufacturer
-safety labels and inscriptions on the device are clearly legible
-the mechanical condition will allow the device to be put to further use
-any soiling has no effect on safety of operation.
The defibrillator electrodes as well as handles and holder recesses must be free of any
cream residue.
The defibrillator electrodes, pacemaker cable, ECG cable , SPO2 cable and CardioServ
power cord should be checked for any visible external damage to the insulation and strain
relief.
10.4 Performance Check
10.4.1 Power-up Test
Switch the instrument on with the energy selector switch (turn rotary switch to first position
ECG).
A chessboard pattern appears on the display for about 2 seconds. A performance test follows
and the software release number is displayed. If the self-test is O.K., no error message appears on the screen. When error message occurs, see page 39 "Error Codes".
10.4.2 Key Test
Press the F1 and F5 keys simultaneously. The configuration screen appears. By pressing
the F3 and F4 keys simultaneously the key test screen appears in the selftest mode.
By pressing each key in turn, the function of the keys can be tested. The key pressed appears in the key test screen with its assigned function. This screen also provides self-test
information. The self-test screen also shows the software version, its checksum and the
results of the CardioServ self-test. The options built into this instrument are displayed alongside the results of the self-test, pacemaker version, VF, date, time and SPO2 version plus
error status.
Version 4.x CardioServ - 61 Revision J 227 483 02
Maintenance and Technical Inspection
10.4.3 Printer Test
The printer is tested in the standard mode. Check that there is some paper and press the Print
key. A manual printout will then be printed out at 25 mm/s.
Using a ruler check the printout grid. In the event of a deviation, reset the motor speed (for
details see section 8 Motor Adjustment).
10.4.4 Energy Test
Connect defibrillation electrodes to Defi. The paddles must be locked in place in the Defi
holders.
Prerequisite for the following test < energy 360 joules in max. 9 seconds>
The Defi battery must be fully charged or the Defi must be connected to the mains with a
power cord.
Switch instrument on. Switch energy selector switch to 360 joules. Energy must be available
after approx. 9 seconds. Trigger energy charge operation by pressing the Charge Defi key in
the electrode handle.
As soon as the charge operation is complete a beep sounds. Release the defibrilla
tion pulse with the Charge Defi key and the Defib key within the next 30 s.
The values (tolerance range) for the energy released is given in the table below.
Energy adjustments must only be made at the factory.
Energy selectedEnergy available/releasedEnergy released
Caution: During the pacemaker test the energy selector switch may be set to the ECG position
only. Do not actuate the Defib and Charge keys.
Connect Defib/Pacer Tester to CardioServ.
Use a set of disposable electrodes (2059144-005 or 2059145-010). Remove insulation on
cable ends and solder banana connectors on them.
Switch CardioServ pacemaker on and select operating mode Fix.
Use the +mA, -mA keys to select the pulse current.
Use the +P/min, -P/min keys to select the pulse rate.
Pulse current and pulse rate shall be within +5% tolerance.
Pulse width Demand, Fix: 40 ms
> 155 P/min20 ms
Switch pacemaker on Defi on and select operating modeDemand.
Use the +mA, -mA keys to select a pulse current between 5 mA and 200 mA.
Use the +P/min, -P/min keys to select a pulse rate of 60 pulses.
Use the ECG simulator and set its pulse rate below 60 pulses. The pacemaker starts pacing.
Set the ECG simulator pulse rate above 60 pulses. In this case the pacemaker stops.
Version 4.x CardioServ - 63 Revision J 227 483 02
Maintenance and Technical Inspection
10.4.6 SPO2 Performance Check
Connect the SPO2 trunk cable to SPO2 input connector of CardioServ.
Connect the SpO2 simulator to the trunk cable. The SPO2 value and the waveform
(plethysmogram) appear after a few seconds on the CardioServ display.
Monitor settings on CardioServ
Activate pulse frequency display by pressing F5 (next), followed by switching to (HR Source
Pulse) with F1 (HR Source Pulse).
Displaying waveforms and parameter readings
-An SpO2 waveform should appear on the screen.
-An SpO2 value according to the table below should be displayed.
-The pulse rate should be displayed according to the table below.
Simulator value SpO2Value displayed
7068% - 72%
9088% - 92%
Simulator value pulse rateValue displayed
601.2% +1 bpm
2001.2% +1 bpm
Remove the SpO2 simulator and connect an SpO2 finger probe. Check if it works correctly.
Connect the electrode cable to the Defi. Use a standard ECG signal generator to generate ECG
signals. Use either a 3-lead trunk cable 223 288 01 or a 5-lead trunk cable 223 419 05 with
5-lead electrode cable 384 018 10.
Switch Defi to monitor mode. The ECG and the heart rate adjusted on the ECG simulator
appear on the display. The upper and lower limits should be tested to ensure they are
enabled. The error messages when electrodes become detached should also be checked. The
error message <Electrode error> appears on the left-hand side of the display. It is important to
ensure that the ECG lead is selected so that the corresponding electrode is tested. In the case
of the paddles lead the error message <Electrode error> appears on the screen when the
paddles are taken out of their holders on the CardioServ.
10.4.8 Cardioversion Test
-Connect the ECG electrode cable to the CardioServ. Use either a 3-lead trunk cable
223 288 01 or a 5-lead trunk cable 223 419 05 with 5 lead electrode cable 384 018 10.
-Connect the ECG leads to the defib tester
-Select 60 BPM ECG pulse rate on defib tester
-Set energy selector switch to any energy setting
-Select sync mode by pressing the Sync key on CardioServ keypad
-Verify that “Sync” appears on display and trigger marks are visible above the QRS
complexes
-Select Sync test on defib tester
-Connect the paddles to the defib tester
-Charge energy
-Simultaneously press and hold the Shock buttons on both paddles. Triggering is affected
by the peak of the QRS complex of the beat. After shock Cardioversion function is
automatically reset.
-If the measured delay time on defib tester is greater than 60ms, the test has failed.
10.4.9 Option Socket Input Test (optional for CardioServ VF)
The option socket input can be tested with the dongle No. 303 445 15 in the configuration. If you
can enable the operating mode Semi-automatic/Dongle in the configuration (press F1 and F5
keys simultaneously) of semi-automatic defibrillators, this indicates that this function is O.K.
Version 4.x CardioServ - 65 Revision J 227 483 02
Maintenance and Technical Inspection
10.5 Battery
A battery charge check can only be performed in the battery service unit Part No.
701 279 01. This tests takes at least 2 hours, max. 3 hours. The service manual for the battery
service unit can be ordered under Part No. 227 494 11.
If no battery service unit is available, the battery should be replaced every 2 years.
Battery Maintenance
Proper maintenance of NiCd batteries is essential and considerably promotes their proper
performance. Routine preventive maintenance should be carried out by qualified service
technicians on a regular basis (recommended interval: 30 days). If batteries are repeatedly
partially discharged, the resulting "memory effect" max dramaticaly reduce the battery
capacity.
This effect can be efficiently minimzied by regular conditioning. If the capacity of a relatively new
battery is drastically reduced, the battery max be reconditioned by repeated charging and
discharging.
Monthly Battery Maintenance (Conditioning) and Checks
1. Disconnect CardioServ from the power line and discharge fully charged battery in the
monitoring mode. To do so, set energy selector switch to (SpO2 sensor not connected)
and wait until device switches off.
2. Check how long it takes before battery is depleted. If the time is less than 1.8 hours, the
battery is too old or improperly maintained and should be replaced.
3. Recharge the battery. This will take 16 hours.
Rechargeable batteries require special maintenance and continued checks to assure they
function in emergency situations. It is normal for batteries of this type to selfdischarge when
not in use.
11. Safety Analysis Test
11.1. General introduction
The suggested Safety Analysis Tests refer to the international standard IEC 601-1.
The tests are generally performed with Safety Testers, on most of them, the measuring circuits according IEC 601 are already implemented.
The following is a general description of the tests to be performed. For the handling of your
Safety Tester follow the user manual.
The tests may be performed under normal ambient conditions of temperature, humidity and
pressure and with line voltage.
The leakage currents correspond to 110 % of rated voltage for the tested unit. Most Safety
Testers take this into account, otherwise the measured values have to be calculated.
11.2 Recommended Test Equipment
- Safety Tester for measurements according to IEC 601.
- Testing connector according to the following description.
11.3 Protective Earth Resistance Test
The protective earth resistance from power connector to any protective earth connected
exposed conductive part is measured.
Because the protected earth is not connected to other touchable conductive parts (contacts to
battery, contacts to car holder) “as a protected earth connection”, the protected earth
resistance test is not necessary. These other touchable conductive parts are grounded just for
EMC reasons.
The protected earth begins at CardioServ AC connector and ends inside the CardioServ
power supply on the left mounting screw, near the power supply line connector.
Notes to check this protected earth connection:
-Specification of test circuit:
-AC current source 50Hz/60Hz of at least 10A up to 25A with limited output voltage
of 6V.
-If resistance is greater than 100 mOhm, the unit fails this test.
Version 4.x CardioServ - 67 Revision J 227 483 02
Safety Analysis Test
11.3.1 Leakage Current Measurement
To perform the suggested measurements, the unit under test has to be separated from any
interconnection to a system. If the unit is part of a system, extended tests according to IEC
601-1-1 have to be performed. The following diagram shows the
Measuring Circuit [M] required for leakage current. The reading in mV corresponds to μA
(leakage current). The Safety Testers generally work with this Measuring Circuit [M] and the
displayed values are already converted to leakage current.
10 k
1 k
0,015 µF
mV
Measuring
instrument/
Calibrator
(Ri >1 M Ω)
11.3.2 Enclosure Leakage Current Test
This test is performed to measure leakage current from chassis to ground during normal conditions (N.C.) and single fault conditions (S.F.C.).
In all cases, the leakage current is measured from any exposed conductive parts to ground,
the unit under test has to be switched on and off.
Connect the unit under test to your Safety Tester.
- During normal conditions (N.C.), referring to the electrical diagram, measurements have to
be done under the following conditions:
* Polarity switchNorm and RVS
* GND switchGND closed
*S1closed and open
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227 483 02 Revision J
Safety Analysis Test
-During single fault conditions (S.F.C.), referring to the electrical diagram, themeasure-
ments have to be done under the following conditions:
* Polarity switch NORM and RVS
* GND switch GND open
*S1 closed
Test has failed if the measured values are greater than:
N.C.S.F.C
100 μA500 μA
300 μA (U.L. requirements)
Electrical Diagram for Enclosure Leakage Current Test
Safety Tester
S1
NORM/RVS
[M]
POWER CORD
UNIT
UNDER
TEST
GND
Probe to exposed
chassis
HIGH
LOW
GND
POWER CORD
11.3.3 Patient Leakage Current Test
This test performs a leakage current test under single fault conditions (S.F.C.) depending on
domestic power outlet with 115 or 230 V AC as source into the floating inputs.
The following signals have a separate floating input and have to be tested separately.
ECG from ECG Input socket
ECG from Paddels
SPO2
In all cases, the leakage current is measured from input jack of unit under test to ground. The
measurement ground point is the left-hand contact on the underside of the CardioServ.
Version 4.x CardioServ - 69 Revision J 227 483 02
Safety Analysis Test
For testing the floating ECG input ,a patient cable, with all leads connected together, is used.
For testing the floating input from Paddles, the test is measured on each Defipaddles.
For testing the floating input from SPO
2 , test plugs are used.
Connect the unit under test to your Safety Tester.
- Referring to the electrical diagram, measurements have to be done under the following
conditions:
227 483 02Service Manual eng CardioServ / CardioServ VF
440 081 80Assembly Instructions CardioServ Car Mounting System
440 082 27Installation Instruction CardioServ Wall Mount System
Defib Paddles
217 304 03Defibrillation Electrode, external, with recorder start, for CardioServ
2030249-001Electrode Lead f. Defib-El.”internal” without contact insert, for CardioServ
926 074 97Handle for spoon electrode
Keypad VF
390 001 52Keypad with Pacemaker ESAOTE/international
390 001 68Keypad without Pacemaker ESAOTE/international
Keypads manual
390 001 56Keypad without pacemaker, international
390 001 57Keypad with pacemaker, international
390 001 58Keypad without pacemaker, ESAOTE
390 001 59Keypad with pacemaker, ESAOTE
Recorder
2033230-001Print Head Service Kit CardioServ
384 015 81Exchange Recorder preman. f. CardioServ
303 434 78Transportation roller
918 083 49Motor 18 V~
480 159 46Gear 10 mm diameter
480 159 47Gear 24 mm diameter
480 159 48Gear 40 mm diameter
388 010 56Pcb. Motor
432 522 30Flap. Recorder
430 517 84Sticker in Flap
Version 4.x CardioServ - 71 Revision J 227 483 02
Spare Parts Lists
Printed circuit boards for Version 4.x
303 445 43Pcb. analog(389 004 22)
388 032 53Pcb. Digital without Pacemaker(389 004 22)
388 032 06Pcb. Digital with Pacemaker(389 004 26)
914 326 45Energy switch mounted on Pcb Digital
929 167 173V Battery on PCB Digital for keep date and time
930 117 26Used up to S/N 101157661, not orderable, Depot repair only
2026753-001Pcb.SPO2 MP507, NELL2-S board, used from S/N 101157662
303 445 32Speaker
903 449 88Capacitor
2034056-020Sticker China RoHS
2002451-001Lower shell
430 518 05Sticker “Attention, high Voltage....”, German
430 518 06Sticker “Attention, high Voltage....”, English
430 518 07Sticker “Attention, high Voltage....”, French
430 518 12Sticker “Attention, high Voltage....”, Italian
430 518 13Sticker “Attention, high Voltage...”, Spanish
430 518 14Sticker “Attention, high Voltage...”, Russian
2028019-001Sticker "Attention, high Voltage...", Chinese (simplified)
2035333-001Sticker "Attention, high Voltage...", Czech
2035553-001Sticker "Attention, high Voltage...", Portuguese
2036666-001Sticker "Attention, high Voltage...", Turkish
2036706-001Sticker "Attention, high Voltage...", Korean
2037298-001Sticker "Attention, high Voltage...", Lithuanian
2039103-001Sticker "Attention, high Voltage...", Polish
2038412-001Sticker "Attention, high Voltage...", Romanian
504 657 54Contact ———> Station
504 657 28 Contact for Paddles
432 522 27latch
432 522 35Filler Plug
924 017 22Foot
482 035 19Knob for Energiy Selector
482 035 21Knob for Energiy Selector (Esaote)
923 096 69Mounting Base
829 074 11Scotch mount, white
In-/Output connector
303 445 38ECG Inputconnector completely wired for CardioServ version 4.x
2006698-001 Distance Case
303 445 39SPO2 Input connector completely wired for CardioServ, used up to
S/N101157661
2026751-001SPO2 Input connector completely wired for CardioServ, valid from
S/N101157662 and higher
303 445 17Inputconnector option Dongel
303 444 16Electrode coupling for paddles (Used for CardioServ Version 3.x and 4.x)
915 417 95Mains plug 3 wire
303 444 22Charge Socket for 12 V (option)
841 202 28Screw
803 083 02 Nut
804 177 06 Washer
Wire Sets
38327322Pace maker cable
38327339Power supply cable
3832729412 Volt cable from analog board to digital board + Batterie cable
Power Supply
930 118 46Switching power supplies
908 122 28Fuse block
912 084 25Fuse T 6,25A
303 440 30Battery Pack 12 V / 1,2 AH
LCD Display
930 117 17 LCD Display (is obsolete)
2007355-001 new LCD Display replace the old Display 930 117 17
Version 4.x CardioServ - 73 Revision J 227 483 02
The car-holder secures the CardioServ during ambulance transport. In this holder the
CardioServ is supplied with power from the 12-volt ambulance power supply system.
CardioServ Wall Holder 202 307 02
The wall holder secures the CardioServ when not in use. It is identical to the car-holder,
except that it does not have any electronics to charge the battery or supply power to the
device.
CardioServ Charging Unit 205 106 01
The charging unit serves to supply power in the CardioServ during vehicle transport. The
CardioServ is supplied with power from the 12-volt vehicle power supply system. Using this
charging unit requires equipping the CardioServ with the charging socket 303 444 22.
Version 4.x CardioServ - 75 Revision J 227 483 02
Accessories: Car holder
Installation Instructions for the CardioServ Mounting System 202 307 01
* First of all, connect the mounting system to the
12-V power supply system of the ambulance (cable
aperture on the underside of the mounting system,
see terminal diagram).
* Connect the positive terminal (+12 V) to the free
contact of the fuse holder (4.8-mm sleeve
enclosed).
Connect earth (0 V) to the corresponding contact of
the terminal block (4.8-mm sleeve enclosed).
Please use the enclosed adhesive fastening base
and the cable tie to fix the connection cables.
Observe the following points when connecting the
mounting system:
-the negative terminal of the ambulance power
supply must be connected to earth,
-the positive lead must be protected with a 10
Amp fuse (slow blow) and
-the lead diameter must be adequate.
* The mounting system has 4 bore holes both at the
top and bottom edges, allowing it to be mounted to
the ambulance in a vertical or horizontal position
(take care that the mounting system is flush against
the wall of ambulance; in the vertical position the
wider part with the cable aperture must face down!)
(see Fig. 1).
* Replace the 4 rubber feet of CardioServ with the
metal feet enclosed. When screwing down the
metal feet, please note that they have a recess on
one side for the screw head.
* Use the appropriate type of screws for attachment
of the metal feet: If the CardioServ unit is equipped
with metal bushings, please use the fillister head
screws DIN 912 M 4 x 12; if there is no metal
bushing but only a hole, please use Plastite screws
4 x 16.
* Please be sure to use the red feet (angular groove)
at the bottom, i.e., on the side with the contacts.
(See Fig. 2).
Figure 1
unlock here
bottom
red
rot
Figure 2
* If required, you may attach the enclosed rubber feet
on top of the metal feet.
* Mount the CardioServ by first inserting the feet at
the bottom, then by introducing the feet at the top.
SpO2 PCB - MP204 930 117 26 D B, C 04,05,07,08 Index C is equivalent: MP204 P Revision A...A/7 (see label CPU)
Index D is equivalent: MP204 P Revision 048685-D (see label CPU)
Used together with PCB Digital 38803206 Index B7,I,J,J1,L,L1,L2,M,N,O
Used together with PCB Digital 38803253 Index B4,F,G,G1,I,I1,I2,J,K,L
Used together with EINBAUDOSE SPO2 30344539
PCB - OXYMETER COVIDIEN 2026753-001 E A, B, C, D 04,05,07,08 Used together with PCB Digital 38803206 effective from Index P
Used together with PCB Digital 38803253 effective from Index M
Used together with CONN RCPT CSERV SPO2 MP507 2026752-001
01, 01-L, 02, 03, 06
GE Medical Systems
Information Technologies GmbH
Munzinger Straße 5
79111 Freiburg, GERMANY
SpO2 PCB - MP204 930 117 26 D B, C 04,05,07,08,12,13,16,17 Index C is equivalent: MP204 P Revision A...A/7 (see label CPU)
Index D is equivalent: MP204 P Revision 048685-D (see label CPU)
Used together with PCB Digital 38803206 Index B7,I,J,J1,L,L1,L2,M,N,O
Used together with PCB Digital 38803253 Index B4,F,G,G1,I,I1,I2,J,K,L
Used together with EINBAUDOSE SPO2 30344539
PCB - OXYMETER NELLCOR 2026753-001 B A 04,05,07,08,12,13,16,17 Used together with PCB Digital 38803206 effective from Index P
Used together with PCB Digital 38803253 effective from Index M
Used together with CONN RCPT CSERV SPO2 MP507 2027652-001
R
O
L
zae -- 083713 PCB revision numbers updated 16.08.06 P. Fischer
zad -- 084160 Index/Compatible of both Lpl. Digital updated 23.05.06 P. Fischer
zac -- 080432 SPO2 section total reworked, V4.1 updated to V4.2 07.07.05 P. Fischer
zab -- 077851 38803206 Index N auf O, 38803253 J auf K, 38803205 H1 auf I 01.09.04 P. Fischer
zaa -- 076988 38803206 von Index M auf N. 38803253 von J auf K 07.05.04 P. Fischer
z -- 075702 217 304 04 Index von Q auf R 20.02.04 P. Fischer
O
,L
L
I
,I
,H
GE Medical Systems IT GmbH
Munzinger Str. 3
D-79111 Freiburg
Copyright GE Medical Systems IT
r - 077851 Digital/Analog: Index geändert 24.11.04 P. Fischer
Marquette Hellige GmbH
Not equipped in Version :
1)
2)
3)
4)
5)
Revision-No
REVISIONS
Index
Date / Name
A04
DRAWN
APPROVED
ISSUED
D-79007 Freiburg
F67211
Date / Name
21.03.96/SNA
11.07.96/SNA
M&E/ALLGEIER
388 032 03 P
LPL DEFI_HWDONGLE
PCB DEFI_HWDONGLE
Sheet:
11
of
[1997, 7, 1, 3]
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
065708
077851
ECO-087521
REVISIONS
Index
A
B
C
Date / Name
20.10.00/MSG
07.10.04/TYR
18.04.07/TYR
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
11.04.96/SNA
05.12.96/HWM
M&E/MIKLOSS
38803205-D02
SCHEMATIC
CServ4_ANALOG
Sheet:
of
111
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
065708
ECO-087521
REVISIONS
Index
A
B
Date / Name
20.10.00/MSG
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
11.04.96/SNA18.04.07/TYR
05.12.96/HWM
M&E/MIKLOSS
38803205-D03
SCHEMATIC
CServ4_ANALOG
Sheet:
of
112
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
202826
203194
065708
ECO-087521
REVISIONS
Index
A
B
C
D
Date / Name
14.04.97/JOK
17.12.97/JOK
20.10.00/MSG
18.04.07/TYR
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
11.04.96/SNA
05.12.96/HWM
M&E/MIKLOSS
38803205-D04
SCHEMATIC
CServ4_ANALOG
Sheet:
311
of
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
202957
065708
ECO-087521
REVISIONS
Index
A
B
C
Date / Name
15.07.97/JOK
20.10.00/MSG
18.04.07/TYR
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
11.04.96SNA
05.12.96/HWM
M&E/MIKLOSS
38803205-D05
SCHEMATIC
CServ4_ANALOG
Sheet:
411
of
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
060305
065708
077851
ECO-087851
REVISIONS
Index
A
B
C
D
Date / Name
18.05.98/MSG
20.10.00/MSG
19.08.04/TYR
18.04.07/TYR
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
11.04.96/SNA
18.04.07/MLM
M&E/MIKLOSS
38803205-D06
SCHEMATIC
CServ4_ANALOG
Sheet:
511
of
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
065708
ECO-087521
REVISIONS
Date / Name
Index
A
20.10.00/MSG
B
18.04.07/TYR11.04.96/SNA
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
05.12.96/HWM
M&E/MIKLOSS
38803205-D07
SCHEMATIC
CServ4_ANALOG
Sheet:
611
of
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
202826
203194
065708
ECO-087521
REVISIONS
Index
A
B
C
D
Date / Name
14.04.97/JOK
17.12.97/JOK
20.10.00/MSG
18.04.07/TYR
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
11.04.96/SNA
05.12.96/HWM
M&E/MIKLOSS
38803205-D08
SCHEMATIC
CServ4_ANALOG
Sheet:
of
117
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
065708
ECO-087521
REVISIONS
Date / Name
Index
20.10.00/MSG
A
18.04.07/TYR11.04.96/SNA
B
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
05.12.96/HWM
M&E/MIKLOSS
38803205-D09
SCHEMATIC
CServ4_ANALOG
Sheet:
811
of
GE Medical Systems
Information Technologies GmbH
Not equipped in Version :
x1
388 032 05
x2
2036591-001
x3
x4
x5
Revision-No
065708
077851
ECO-087521
ECO-091271
REVISIONS
Index
A
B
C
D
Date / Name
20.10.00/MSG
19.08.04/TYR
18.04.07/TYR
29.05.08/TYR
A03
DRAWN
APPROVED
ISSUED
D-79111 Freiburg
Munzinger Str. 3
43367213
Date / Name
11.04.96/SNA
Electronically in Agile
M&E/MIKLOSS
38803205-D10
SCHEMATIC
CServ4_ANALOG
Sheet:
911
of
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