NOTE: Due to continuing product innovation, specifications in this
manual are subject to change without notice.
Trademarks Trademarked names appear throughout this document. Rather than list
the names and entities that own the trademarks or insert a trademark
symbol with each mention of the trademarked name, the publisher states
that it is using the names only for editorial purposes and to the benefit of
the trademark owner with no intention of improperly using that
trademark.
ACCUSKETCH, AccuVision, APEX, AQUA-KNOT, ARCHIVIST,
Autoseq, BABY MAC, CardioServ, CardioSmart, CardioSys,
CardioWindow, CASE, CD TELEMETRY, CENTRA, CHART GUARD,
CINE 35, CORO, COROMETRICS, CRG PLUS, Digistore, Digital
DATAQ, E for M, EAGLE, Event-Link, HELLIGE, IMAGE STORE,
INTELLIMOTION, LASER SXP, MAC, MAC-LAB, MACTRODE,
MARQUETTE, MARQUETTE MAC, MARQUETTE UNITY NETWORK,
MARS, MAX, MEDITEL, MEI, MEI in the circle logo, MEMOPORT,
MEMOPORT C, MINISTORE, MINNOWS, Monarch 8000,
MULTI-LINK, MULTISCRIPTOR, MUSE, MUSE CV, Neo-Trak,
OnlineABG, OXYMONITOR, Pres-R-Cuff, PRESSURE-SCRIBE, QMI,
QS, Quantitative Medicine, Quantitative Sentinel, Qwik Connect Spiral,
RAMS, RSVP, SAM, SEER, SOLAR, SOLARVIEW, Spectra 400,
Spectra-Tel, ST GUARD, TRAM, TRAM-NET, TRAM-RAC,
TRAMSCOPE, TRIM KNOB, UNITY logo, UNITY NETWORK, Vari-X,
Vari-X Cardiomatic, VariCath, VAS, and Vision Care Filter are
trademarks of GE Medical Systems Information Technologies registered
in the United States Patent and Trademark Office.
12SL, 15SL, AccuSpeak, ADVANTAGE, BAM, BODYTRODE,
Cardiomatic, CardioSpeak, CD TELEMETRY .-LAN,
CENTRALSCOPE, Corolation, Corometrics Sensor Tip, Dash, EDIC, HI-RES,
IMAGE VAULT, IMPACT.wf, INTER-LEAD, IQA, LIFEWATCH,
MARQUETTE MEDICAL SYSTEMS, MARQUETTE . RESPONDER,
MENTOR, MicroSmart, MMS, MRT, MUSE CardioWindow,
O 2 SENSOR, OMRS, Premium, RAC, SILVERTRACE, SMART-PAC,
SMARTLOOK, Spectra-Overview, Trimline, UNITY, and Universal are
trademarks of GE Medical Systems Information Technologies
ANUAL INFORMATION ....................................................................................................................................4
OW TO REACH US .........................................................................................................................................10
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1 INTRODUCTION
1.1 Manual Information
Scope of the Manual
The content of this field service manual is aimed primarily at biomedical
equipment technicians and field service personnel. The user of this field
service manual is expected to have a solid background in electronics,
including strong backgrounds in analog and digital electronics, as well as
microcomputer technology familiarity.
Revision History
Each page of this manual has a revision letter located at the bottom of
the page. It identifies the revision level of the entire manual. This may
be important if you have different manuals and you don’t know which is
the most current.
For the initial release, all pages have the revision letter A. For the second
update, all pages receive the revision letter B. The latest letter of the
alphabet added to the table below corresponds to the most current
revision.
Revision History
RevisionDateComment
A04.05.2001Initial release of this document
Manual Purpose
This field service manual has been prepared by the technical
publications staff at GE Medical System - IT, Inc. It is intended for
use by biomedical electronic technicians or other qualified service
personnel responsible for installation, maintenance or repair of the
RAB or RAB RL.
Chapter Content
The field service manual is organized into sections, as follows:
Introduction
Chapter one, “Introduction”, describes the revision history,
manufacturer responsibility, notes/cautions/warnings
and abbreviations.
Equipment Overview
Chapter two, “Equipment Overview”, describes the product,
technical specifications, preparation for use
and theory of operation.
Maintenance
Chapter three, “Maintenance”, describes the maintenance schedule,
visual inspection, cleaning the monitor, checkout procedures, leakage
current tests and “Blink Mode speciality”.
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Troubleshooting
Chapter four, “Troubleshooting”, describes electro-static discharge,
service mode and FAQ’s
Chapter six, “Connectors”, describes pin assignment of the connectors.
Assembly Drawings
Chapter seven, “Assembly Drawings”, provides mechanical diagrams,
reference diagrams, schematic diagrams and parts lists.
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1.2 Safety Information
Responsibility of the
Manufacturer
GE Medical Systems is responsible for the effects of safety,
reliability, and performance only if:
•Assembly operations, extensions, readjustments, modifications, or repairs are carried out by persons
authorized by GE Medical Systems.
•The electrical installation of the relevant room complies with the requirements of the appropriate
regulations.
•The equipment is used in accordance with the instructions for use.
Intended Use
This device is intended for use under the direct supervision of a licensed
health care practitioner.
To ensure patient safety, use only parts and accessories manufactured or
recommended by GE Medical Systems.
Contact GE Medical Systems for information before connecting
any devices to this equipment that are not recommended in this manual.
Equipment Symbols
The following symbols appear on the equipment.
NOTE
Some symbols may not appear on all equipment.
ATTENTION: Consult accompanying documents before using the
equipment.
Consult accompanying documents
AC voltage
DC voltage
LED indicator
Protection class II
(Caution the power supply unit for the alarm light of RAB RL is
a protection class I device)
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Notes, Cautions, and
Warnings
The safety statements presented in this section apply to the components
of the RAB and RAB RL Remote Alarm Box. Look for additional safety
information throughout the rest of this manual.
The order in which safety statements are presented in no way implies
order of importance.
The terms WARNING, CAUTION, and NOTE are used throughout this
manual to point out hazards and to designate a degree or level or
seriousness. Familiarize yourself with their definitions and significance.
Hazard is defined as a source of potential injury to a person.
WARNING
indicates a potential hazard or unsafe practice which, if
not avoided, could result in death or serious injury.
CAUTION
indicates a potential hazard or unsafe practice which, if
not avoided, could result in minor personal injury or
product/property damage.
NOTE
provides application tips or other useful information to
assure that you get the most from your equipment.
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1.3 Service Information
Service Requirements
Follow the service requirements listed below.
• Refer equipment servicing to GE Medical Systems authorized service personnel only.
• Any unauthorized attempt to repair equipment under warranty voids that warranty.
• It is the user’s responsibility to report the need for service to GE Medical Systems or to one of their
authorized agents.
•Failure on the part of the responsible individual, hospital, or institution using this equipment to
implement a satisfactory maintenance schedule may cause undue equipment failure and possible
health hazards.
•Regular maintenance, irrespective of usage, is essential to ensure that the equipment will always be
functional when required.
Equipment
Identification
Every GE Medical Systems device has a unique serial number for
identification.
Warranty
1 year
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1.4 Terminology
RABRemote Alarm Box
RAB RLRemote Alarm Box with Remote Light
UTP CABLEUnshielded Twisted Pair Cable
PFDPower Failure Detection Mode of RAB / RAB RL
PWAPrinted Wire Assembly
DMMDigital Multi Meter
GEMS-IT GE Medical Systems Information Technologies
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1.5 How to Reach Us
Service Calls and Product Support
To open a service call or obtain product support call the numbers below:
or contact your representative or distributor
For other product information please contact one of the offices listed on
the next page.
Ordering Supplies &Service Parts
Order supplies (leadwires, electrode paste, thermal paper, etc.)or service
parts (manuals, circuit boards, cables, software, etc.)from:
800.558.7044 (US &Canada)
561.575.5000 (outside US)
Accessories
GE Medical Systems Accessories and Supplies
2607 North Grandview Blvd.
Mail Code:SN-471
Waukesha,WI 53188
Telephone: 800.558.5102 (US only)
262.521.6856 (outside U.S.)
Fax:800.232.2599 (US only)
262.521.6855 (outside US)
Service Parts
GE Clinical Services
P.O.Box 9100,100 Marquette Drive
Jupiter,FL 33468-9100
Telephone: 800.558.7044 (US only)
561.575.5000 (outside US)
Fax:800.421.6841 (US only)
561.575.5050 (outside US)
Have the following information available before calling:
♦ part number of the defective part, or
♦ model and serial number of the equipment,
♦ part number/name of the assembly where the item is used,
♦ item name, and
♦ where applicable, reference designation (eg,R13,S12).
Ordering Manuals
When ordering additional operator manuals, be sure to include the
software version of the product.
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Other Questions or Problems
For additional information contact one of the offices listed below or see
our website at www.gemedicalsystems.com
Headquarters
GE Medical Systems
Information Technologies
8200 West Tower Avenue
Milwaukee,WI 53223,USA
Telephone: 414.355.5000 or 800.558.5120 (US only)
Fax:414.355.3790
Europe
GE Medical Systems
Information Technologies
Postfach 60 02 65
D-79032 Freiburg, Germany
Telephone: +49.761.4543.0
Fax:+49.761.4543.233
Australia
GE Medical Systems (Australia)Pty Ltd.
13 South Street
Rydalmere NSW 2116,Australia
Telephone: +61.2.9975.5501
Fax:+61.2.9975.5503
Japan
GE Medical Systems,Japan
67-4 Takakura-cho
Hachiojii-shi,Tokyo 192-003,Japan
Telephone: +81.42.648.2944
+0120-055-919 (toll free inside Japan only)
Fax:+81.24.648.2902
Hong Kong
GE Medical Systems Hong Kong Limited
11th Floor,The Lee Gardens
33 Hysan Avenue
Causeway Bay,Hong Kong
Telephone: +852.2100.6300
Fax:+852.2100.6292
Southeast Asia
GE Pacific
298 Tion Bahru Road #15-01/06
Central Plaza,Singapore 168730
Telephone: +65.277.7620
Fax:+65.277.7600
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2 EQUIPMENT OVERVIEW
2.1 Product Description
Remote Alarm Box (RAB)
The Remote Alarm Box is a microprocessor controlled isolation
relay (secondary alarm device).
It is used to connect the device listed below to the hospital alarm
system:
• Dash patient monitors
• Dash Port Docking Station
Figure 2.1 Remote Alarm Box
• Solar 8000M patient monitor
Remote Alarm Box with Remote Light (RAB RL)
The RAB RL is used to connect an alarm light (Remote Light, P/N
8500 AAX) to the devices listed above (secondary alarm light). This
RAB RL does not connect to the hospital alarm system. A special,
hospital grade power supply unit is required to supply power to the
alarm light;
This unit is included in the shipment.
Figure 2.2 Remote Alarm Box RAB RL
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Both, RAB and RAB RL will function correctly only in conjunction with monitors with the software versions
listed below:
MonitorSoftware Version
Dash 2000V3A or later
Dash 3000
Dash 4000
Solar8000MV2A or later
1)
not via Dash Port Docking Station
V2B
V2B
1)
or later
1)
or later
Table 2.1 RAB Software compatibility
2.2 LED Indicator Description
Figure 2.3 RAB LED Interface
Explanation of the LED Indicator
IndicatorFunction
indicate the selected alarm
A, B, C
mode:
A : continuous mode
B : intermittent mode
C : blink mode
D
mode with power failure
detection
E
lights up in alarm situation
Table 2.2 LED Indicator
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2.3 Description of Operation
Figure 2.4 RAB Block Diagram
Block diagram of RAB :
The interface to the connected Patient Monitoring System is realized by a standard serial RS232
communication interface. So, in different to the existing Isolation Boxes („Nurse Call Boxes“) a small
microprocessor is needed to realize the communication part of the box. The RAB / RAB RL operation
mode could be configured by three configuration jumpers.
The µProcessor is requesting every 500ms the alarm status of the patient monitor via serial communication
protocol. If the Monitor is in “ALARM”-state, the RAB / RAB RL toggles the alarm relay according to the
configured alarm mode. If the Monitor is not in this state, the RAB / RAB RL switches the relay back (if it
was in alarm state) or the relay remain the “non-alarm” position according to the configured operating mode.
After power up of the RAB / RAB RL there is a onetime switch delay of approx. 20 seconds to let the patient
monitor startup to normal operation.
An independent hardware watchdog / power supervisor chip is provided to guarantee proper powerup/
powerdown and software behavior.
The configured device status and also the detected alarm status are displayed by 5 LED’s.
On Patient Monitor side the communication interface is realized as a M-Port interface with an 8-pin RJ-45
connector.
To connect the box to a hopsital alarm call system a 3 terminal screwing connector is provided and to
connect the RL version of the RAB to the EAGLE Remote Light and external IEC601-1 power supply, a 9pin SUB-D and a 3-pin power connector are used .
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3 MAINTENANCE
3.1 Maintenance Schedule
Manufacturer
Recommendation
To make sure the RAB / RAB RL remains in proper operational and functional
order, a good maintenance schedule must be adhered to.
The manufacturer's recommendations in this regard are as follows:
•Visual Inspection: These should be performed by qualified service personnel upon receipt of the
equipment, every 12 months thereafter, and each time the monitor is serviced.
• General Cleaning: Service personnel should perform this after servicing the monitor.
• Checkout Procedures: These should be performed by qualified service personnel upon receipt of the
equipment, every 12 months thereafter, and each time the monitor is serviced.
•Leakage Current Tests: These should be performed by qualified service personnel upon receipt of the
equipment, every 12 months thereafter, and each time the monitor is serviced.
•Maintenance “Blink Mode” : If Blink mode is used a special maintenance must be performed by
qualified service personnel every 12 months.
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3.2 Visual Inspection
Inspecting the
Monitor
The RAB / RAB RL should be carefully inspected.
Follow these guidelines when inspecting the equipment:
•Carefully inspect the RAB / RAB RL for obvious physical damage to the outer case. Do not use the RAB
/ RAB RL if physical damage is determined. Refer damaged equipment to qualified service personnel
for repair before using it again on a patient.
•Inspect all external connectors, front and rear, for degraded pins, prongs and connector housings.
Refer damaged equipment to qualified service personnel for repair before using it again on a patient.
•Inspect all cable insulation, cable strain-reliefs and cable connectors for damage, cracks or
degradation. Refer damaged equipment to qualified service personnel for repair before using it again on
a patient.
For RAB RL check the fixing of the power cable at power supply and the RAB RL.
•Safety labels and inscriptions on the device are clearly legible.
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3.3 General Cleaning
Clean External
Surfaces
The exterior surfaces may be cleaned with a lint-free cloth dampened
with one of these approved solutions:
• ammonia (diluted),
• Cidex,
• mild soap (dissolved), or
• sodium hypochlorite bleach (diluted).
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3.4 Checkout Procedures
Checkout Procedures
The following pages contain the checkout procedures for the RAB / RAB RL. The purpose of the checkout
procedures is to provide service personnel with a method which can be used to verify operational and
functional performance of the RAB / RAB RL. Failure to attain any of the listed results
indicates a potential malfunction of the RAB / RAB RL. Perform the checkout procedures upon receipt of
the RAB / RAB RL, every twelve months thereafter, and each time the circuit board is removed or replaced.
The checkout procedures are based on the assumption that the RAB / RAB RL being tested is used with
known good cables and test equipment. It also requires that the user be somewhat familiar with the
operation of all test equipment required for the checkout procedures. For more information concerning the
operation of these components, refer to the respective operator manual.
Functional Test
It’s recommended that the RAB / RAB RL will be checked connected to a
complete system with DASH2000, DASH 3000, DASH4000 or
SOLAR8000M as a bedside.
For the functional test switch the monitor to a “NO Alarm” state.
RAB / RAB RL ModeRelay
Intermittent Mode with PFDclosed
Intermittent Modeopen
Continuous Mode with PFDclosed
Continuous Modeopen
Blink Mode with PFDclosed
Blink Modeopen
Test Mode for Service onlyOpen for 0.5 seconds and
Closed for 0.5 seconds,
periodical
Table 3.1 RAB Function Test
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After this change the monitor to a “Alarm “ state.
RAB / RAB RL ModeRelay
Intermittent Mode with PFDOpen for 100 seconds and
Closed for 1 seconds,
intermittent
Intermittent ModeClosed for 100 seconds and
Open for 1 seconds,
intermittent
Continuous Mode with PFDopen
Continuous Modeclosed
Blink Mode with PFDOpen for 2 seconds and
Closed for 2 seconds,
intermittent
Blink ModeClosed for 2 seconds and
Open for 2 seconds,
intermittent
Test Mode for Service onlyOpen for 0.5 seconds and
Closed for 0.5 seconds,
periodical
Table 3.2 RAB RL Function Test
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3.5 Electrical Safety Test
General
Electrical safety test provide a method of determining potential electrical health hazards to the patient or
operator of the device exist.
Recommendations
To help you establish a systematic maintenance routine, GEMS-IT
recommends that you perform all safety tests presented in this
chapter
• upon receipt of the device,
• every twelve months thereafter,
• each time the main enclosure is disassembled or a circuit board is removed, tested, repaired, or
replaced, and
•record the date and results on the “Maintenance/Repair Log” included at the end of this chapter.
CAUTION
Failure to implement a satisfactory maintenance schedule may cause undue equipment failure and
possible health hazards. Unless you have an Equipment Maintenance Contract, GE Medical Systems
does not in any manner assume the responsibility for performing the recommended maintenance
procedures. The sole responsibility rests with the individual or institution using the equipment.
GEMS-IT service personnel may, at their discretion, follow the procedures provided in this manual as
a guide during visits to the equipment site.
Test Conditions
Electrical safety tests may be performed under normal ambient conditions of temperature, humidity, and
pressure.
Test Equipment
The manufacturer recommended test equipment required to perform electrical safety tests is listed below
(see table 3.3). Equivalent equipment may be substituted as necessary.
Required Tools/Special Equipment
Leakage Current Tester
120 V
240 V (equivalent to the figures 3.1 - 3.2)
Multimeter 0 – 1000mV
Table 3.3 RAB Safety Test special Equipment
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Wall Receptacle Test
Before starting the tests, the wall receptacle from which the monitoring device will get electrical power must
be checked. This test checks the condition of the wall receptacle to ensure correct results from leakage
tests. For international wall receptacles, refer to the internal standards agencies of that particular country.
Use a digital multimeter to ensure the wall receptacle is wired properly. If other than normal polarity and
ground is indicated, corrective action must be taken before proceeding. The results of the following tests will
be meaningless unless a properly wired wall receptacle is used.
3.5.1 Ground (Earth) Wire Leakage Current Tests
This test needs to be performed only with RAB RL.
Perform this test to measure current leakage through the ground (earth) wire of the equipment during
normal operation.
1. Set the leakage tester switches as follows:
• GND switch - OPEN,
• Polarity switch – NORM and RVS
• Power switch - OFF.
2. Connect the DMM to the METER jacks on the leakage tester. Set the DMM to measure
AC millivolts.
3. Connect the power cord of the device under test to the power receptacle on the rear
of the leakage tester.
NOTE
The device under test is to be tested at its normal operating voltage.
4. Set the leakage tester power switch to ON.
5. Read the current leakage indicated on DMM. If the reading is greater than the appropriate
specification below, the device under test fails and should be repaired and tested again.
•300 microamperes (0.3 volts on the DMM), and the device under test is powered
from 100 - 120 V / 50 - 60 Hz
•300 µA (0.3 volts on the DMM), and the device under test is powered
from a centered-tapped 200 - 240 V / 50 - 60 Hz, single- phase circuit
•500 µA (0.5 volts on the DMM), and the device under test is powered
from a non-center-tapped, 200 - 240 V / 50 - 60 Hz, single-phase circuit
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NOTE
Center-tapped and non-center-tapped circuits produce
different leakage currents and the UL and IEC limits are
different.
6. Set the leakage tester power switch to OFF.
Figure 3.1 RAB Ground (Earth) Wire Leakage Current Tests
NOTES
The MD (measuring device) is the circuitry defined by the appropriate standard
for measuring leakage current. The measuring devices, defined by various
standard organizations (IEC, UL, etc.), produce almost identical test measurement results.
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3.5.2 Enclosure Leakage Current Test
This test needs to be performed only with RAB RL.
Perform this test to measure current leakage through exposed
conductive surfaces on the device under test during normal operation.
1. Set the leakage tester switches as follows:
• GND switch - OPEN,
• Polarity switch – NORM
2. Connect a meter lead between the GND of the tester accordingly to the circuit and the
metal housing of the RL connector and one of the metal screws of the remote light..
3. Set the leakage tester power switch to ON.
4. Read the current leakage indicated on DMM. If the reading is greater than the
appropriate specification below, the device under test fails and should be repaired and
tested again.
•300 microamperes (0.3 volts on the DMM), and the device under test is powered
from 100 - 120 V / 50 - 60 Hz
•300 µA (0.3 volts on the DMM), and the device under test is powered
from a centered-tapped 200 - 240 V / 50 - 60 Hz, single phase circuit
•500 µA (0.5 volts on the DMM), and the device under test is powered
from a non-center-tapped, 200 - 240 V / 50 - 60 Hz, single-phase circuit
NOTE
Center-tapped and non-center-tapped circuits produce different leakage currents and
the UL and IEC limits are different.
5. Set the polarity switch to RVS and observe the same meter readings as in the previous step.
6. Set the GND switch on the leakage tester to CLOSED.
7. Read the current leakage indicated on DMM. If the reading is greater than the appropriate
specification below, and the device under test is powered from 100-240 V/50-60 Hz,
the device under test fails and should be repaired and tested again.
•100 microamperes (0.1 volts on the DMM), and the device under test is powered
from 100-240 V/50-60 Hz
8. Set the polarity switch to RVS and observe the same meter readings as in the previous step.
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9. Set the leakage tester power switch to OFF and remove the meter lead connected in step 2.
Figure 3.2 Enclosure Leakage Current Test
Test Completion
Disconnect all test equipment from the device. Disconnect the device
power cord plug from the leakage tester power receptacle. Disconnect the
leakage tester from the wall receptacle.
3.6 Maintenance Blink Mode
Due of the maximum switching cycle of the relay contacts there is a reduced relais life time in Blink Mode.
If the Blink mode is used, the PWA must be replaced every 12 months.
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4 TROUBLESHOOTING
4.1 Electrostatic Discharge (ESD)
CMOS Components
The monitor makes extensive use of CMOS components because they are more immune to noise and
consume less power than standard TTL or NMOS components. However, CMOS components are
inherently more susceptible to electrostatic discharge (ESD) damage than other types of semiconductor
materials. ESD damage, causing a weakening or complete breakdown of p-n junctions within multilayer
semiconductor substrates, can range from slight degradation to catastrophic failure. Slight degradation
usually results in intermittent failure of the affected component catastrophic failure results in rendering the
affected component permanently unusable. Although CMOS components may be more sensitive to ESD, all
semiconductor devices are susceptible to ESD damage. All external connector inputs and outputs of the
monitor are designed with protection from ESD damage. However, if the monitor requires service, exposed
components and assemblies contained within are susceptible to ESD damage. This includes human hands,
non-ESD protected work stations and/or improperly grounded test equipment. The following guidelines help
make a service workstation more resistant to the ESD damage:
•Discharge any static charge you may have built up before handling semiconductors or assemblies
containing semiconductors.
•A grounded, antistatic wristband (3M part number 2046 or equivalent) or heel strap should be worn at
all times while handling or repairing assemblies containing semiconductors.
• Use properly grounded soldering and test equipment.
• Use a static-free work surface (3M part number 8210 or equivalent) while handling or working on
assemblies containing semiconductors.
•Do not remove semiconductors or assemblies containing semiconductors from antistatic containers
(Velo-stat bags) until absolutely necessary.
• Make sure power to an assembly is turned off before removing or inserting a semiconductor.
• Do not slide semiconductors or electrical/electronic assemblies across any surface.
• Do not touch semiconductor leads unless absolutely necessary.
• Semiconductors and electrical/electronic assemblies should be stored only in antistatic bags or boxes.
These guidelines may not guaranty a 100% static-free workstation, but can greatly reduce the potential
for failure of any electrical/electronic assemblies being served.
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4.2 RAB / RAB RL for your Safety
Before opening the RAB, please disconnect the cable to the hospital alarm system from the wall inlet to
prevent the risk of higher voltage inside the RAB.
For RAB RL also disconnect the power supply cable before opening the RAB RL.
After configuration of the device to the alarm mode used in the specific hospital and closing / mounting of
the device, always a functional test of the complete alarm path (Patient Monitor -> RAB / RAB RL ->Hospital Alarm System / Remote Alarm Light with external power supply) must be performed!
4.3 Service Mode RAB / RAB RL
For a functional control of the RAB / RAB RL installation without using a Patient Monitor, a special service
mode is implemented. After open the RAB / RAB RL box please configure the configuration jumpers to
SERVICE MODE (J1:2-3, J2:2-3, J3:2-3). Please remember the original settings of the jumpers to
reconfigure the device to the original settings.
This mode is only for service purposes. It will toggle the relay output every half second. This mode toggles
also LED E every half second from ON to OFF and vice versa . It helps to ensure the functionality of the
RAB / RAB RL microprocessor system , the relay output and the connected hospital alarm system / remote
alarm light.
NOTE
When in working in this mode there will be no failure detection or alarm processing! Using this mode
there will be no test of the alarm communication path from the patient monitor to the RAB / RAB RL!
(Patient Monitor, cable, RAB / RAB RL communication interface are not tested).
NOTE
After reconfiguration of the device to the alarm mode used in the specific hospital and closing /
mounting of the device, always a functional test of the complete alarm path must be performed!
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4.4 Troubleshooting FAQ’s
This section covers (when not specifically mentioned) both devices, RAB and RAB RL
No reaction of the RAB / RAB RL after power up
If the RAB / RAB RL will not react on connecting it to a patient monitor / docking station there could be the
following listed reasons for this behavior: When used with DASH / DASH PORT docking station a AUX-Port
to M-Port Adapter must be used at patient monitor / DASH PORT docking station side. When used with
SOLAR8000M, no adapter must be used. Cable to patient monitor could be defective or has no contact to
the patient monitor / docking station connector or the RAB / RAB RL connector AUX-Port to M-Port Adapter
could be defective or has no contact At patient monitor side, cable is plugged into wrong connector (DASH > Ethernet) or the RAB could be defective. Please replace the RAB / RAB.
Patient Monitor’s or Docking Station’s M-port / AUX-Port has a defect.
After power up, not all LED’s are flashing ON for a short time
After powering the device, all five LED’s must flash ON for nearly a second. This is a visual control of the
LED’s circuits functionality. If this error occurs, LED, LED transistor or specific microcontroller output could
have a malfunction. Please replace the RAB / RAB.
Error detected, all five LED’s are blinking
There are several tests done by the internal microprocessor during startup and normal operation of the
device. Because all tests check functional critical parts of the device, a detected error means that the
correct functionality of the device can not be guaranteed. Please replace the RAB / RAB.
RAB / RAB RL works normal, but no relay toggle / LED “E” ON when alarm
There can be the following listed reasons for this behavior: Cable to patient monitor / docking station or
AUX-Port to M-Port adapter is defective or RAB is defective Please replace the RAB / RAB. Patient
Monitor’s or Docking Station’s M-port / AUX-Port has a defect.
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RAB / RAB RL works normal, also in alarm state,
but no reaction of Alarm System:
Check complete cabling to the hospital Alarm System Check hospital Alarm System functionality
Check the fuse inside the RAB. If the fuse was burned, please replace the RAB. Check the functionality of
the RAB relay. To do this, disconnect the RAB from the Alarm System and use an Ohm Meter to check the
correct functionality of the relay. If the relay / LED E will not work properly, please replace the RAB.
RAB RL:
Check the 12 VDC of the medical power supply. If the power supply is defective, please replace it. Check
the wiring inside the RAB RL for broken connections. When the power supply is connected to the RAB RL,
verify the voltages at the RAB RL remote light connector. (See 4.3.3 pinning). If the voltages are OK (also
when in alarm state -> +12VDC on pin ALARM) and the remote light will not work, please replace the alarmlight. Check the fuse inside the RAB. If the fuse was burned, please replace the RAB RL. This should never
happen, if it will, also the power supply and the remote light will surely be defective. Check the functionality
of the RAB relay. To do this, disconnect the RAB RL from the Alarm System and use an Ohm Meter to
check the correct functionality of the relay. If the relay / LED E will not work properly, please replace the
RAB RL.
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5 CONFIGURATION
5.1 CONFIGURATION Jumper
Alarm Mode Configuration (RAB / RAB RL)
Figure 5.1 Jumper Description (Example)
Table 5.1 Alarm Mode Jumper
The factory default setting for the alarm mode is
the “Intermittent Mode (100 seconds) with
Power Failure Detection”. If your application
requires a different alarm mode, configure this
mode as follows before connecting the RAB /
RAB RL.
• Remove the 4 screws on the underside of the housing.
• Take off the upper part of the housing.
You will see the three jumpers J 1, J 2 and J 3 on
the PWA. The jumper configuration determines
the alarm mode (Figure 5.1). Upon delivery, all
three jumpers are in position 1-2 (intermittent
mode – 100 seconds, with power failure
detection). Refer to Table 5.1 for all possible
jumper configurations.
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5.2 Connecting the Cable to the Hospital Alarm System
Warning
Patient Safety — Choose cables and connectors with the appropriate voltage
and current carrying capacity.
Note
When operating the hospital alarm system in the current monitoring mode,
please connect the cables appropriately.
• Loosen the screw of the cable collar on the PWA.
• Guide the cable through the sleeve.
• Connect the cable to the relay contacts as required for the configured alarm mode:
- terminals REL 2 and REL 3: break contact
(open when relay attracts)
- terminals REL 1 and REL 2: make contact
(closed when relay attracts)
•Secure the cable with the collar. To ensure that thin cables are securely held in place by the cable
collar, wrap them in insulating tape or reinforce them with shrink-down tubing.
•Place the upper part of the housing on the lower part, checking the correct position of the optical light
guides.
•Screw tight the four screws on the underside of the housing.
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5.3 Connecting the Alarm Light (RAB RL)
The factory default wiring of the alarm light
connector (1, Figure 5.2) is for an alarm mode
with power failure detection, i.e., when the relay
is released, the light is on. To select a mode
without power failure detection, change the
wiring internally as follows:
Figure 5.2 Connecting RAB RL
• Open the housing and disconnect the cable to terminal REL 3 and connect it to terminal REL 1.
• Close the housing.
• Connect the alarm light to connection (1, Figure 5.2).
• Secure the connection with the screws provided on the plug.
4
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5.4 Connecting the Power Supply Unit (RAB RL)
Note
You can install the power supply unit either by means of a Velcro strip attached to the back side of
the support, or mount it to a GCX system. When using a GCX system, the appropriate fixation
elements must be mounted on the support before the power supply unit can be inserted in the
support.
• Remove the upper part of the cable collar (6, Figure 5.3).
• Plug the power supply cable into the socket (5, Figure 5.3).
• Place the cable in the lower part of the cable collar
(6, Figure 5.3) and screw tight the upper part of the collar
to secure the able.
• Insert the power supply unit (the legs pointing down) in
• Screw the bracket with the cable collar on to the support
• Remove the upper part of the cable collar (9 Figure 5.5).
• Place the power cord in the lower part of the cable collar and
• Connect the power supply unit to the power line.
Figure 5.3 RAB RL connecting power supply
the support (7 Figure 5.4).
(8 Figure 5.5).
Connect the lower cord to the power supply unit.
screw tight the upper part of the collar to secure the
cable (10, Figure 5.6).
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Figure 5.4 a) RAB RL mounting the power supply
Figure 5.5 b) RAB RL mounting the power supply
Figure 5.6 c) RAB RL mounting the power supply
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5.5 Connecting RAB / RAB RL to the Patient Monitor
Caution
Patient Safety — Only the GEMS IT supplied UTP cable or an equivalent cable may be
used to connect the device to the patient monitor. Observe the following points to ensure
correct functioning of the RAB / RAB RL: unshielded, twisted-pair cable, 8-pole,
max. length 5 m, min. AWG 26, gold-plated contacts; do not use X-cables.
•Plug the supplied UTP cable into socket.To do so, push the plug into the socket until you hear it click
into place. Briefly pull on the cable to check that the connection is secure. When connecting the device
to a Dash patient monitor or to a Dash Port Docking Station, the adapter ADPTR AUTOPORT M-PORT
(2001973-001) must be connected to the AUX port of the monitor / Dash Port Docking Station first
(Figures 5.7).
When connecting the device to a SOLAR 8000M patient monitor, the cable is directly plugged into one
of the M-PORT sockets (Figures 5.8).
•Connect the cable as shown in Figures 5.7 and 5.8. Ensure that the connector(s) engage properly.
Figure 5.7 RAB M-Port to Autoport Adapter
Figure 5.8 RAB M-Port UPT cable
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6 Connectors
General
The connector to the Patient Monitor is directly M-Port compatible, so the RAB could be connected directly
to a SOLAR8000M patient monitor.
To connect the RAB to a DASH patient monitor, the Autoport adapter PN 2001973-001, Rev.B or newer
must be used.
Monitor Connector RJ-45
Figure 6.1 RAB / RAB RL RJ-45 Connector
Pinning:
PIN No.LabelDirection/ PowerDescription
1ETH1N.a.M-Port Signal, not used
2ETH2N.a.M-Port Signal, not used
3SIDI/OSerial Identification Pin,
1-Wire Protocol
4M_PORT_GNDPowerGround return line
5TXDOutputRS 232 Transmit line
6SID_RETURNPowerSerial Identification, Ground return line
7RXDInputRS232 Receive line
8M_PORT_VCCPower+5V Power Input
Table 6.1 RAB / RAB RL RJ-45 Connector
Input Data
SIDInput signal to communicate from Patient Monitor (e.g. with M-Port,
like SOLAR8000M) with the DS2430A E²PROM to determine Serial ID
number.
RXD Input signal to get patient monitor alarm status via RS232 communication
Output Data
TXD Output signal to request patient monitor alarm status via RS232 communication.
ETH1,ETH2 M-Port Ethernet differential lines, not connected, not used
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Power Signal
M_PORT_VCCPower input signal (5V)
M_PORT_GNDPower Ground
SID_RETURNPower Ground signal from Patient Monitor (e.g. with M-Port, like
SOLAR8000M) to determine Serial ID number
6.1 Hospital Alarm System Connector
Figure 6.2 RAB Hospital Alarm System Connector
REL1
REL2
REL3
Figure 6.3 RAB Hospital Alarm System Connector - Schematic
REL1Contact to be connected with REL2 if relay current is switched on
REL2Middle contact of the relay
REL3Contact to be connected with REL2 if relay is not powered
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How to connect the cable to Hospital Alarm System
• Loosen the screw of the cable collar on the PWA.
• Guide the cable through the sleeve.
• Connect the cable to the relay contacts as required for the configured alarm mode:
- terminals REL 2 and REL 3: break contact
(open when relay activates)
- terminals REL 1 and REL 2: make contact
(closed when relay activates)
•Secure the cable with the collar. To ensure that thin cables are securely held in place by the cable
collar, wrap them in insulating tape or reinforce them with shrink-down tubing.
•Place the upper part of the housing on the lower part, checking the correct position of the optical light
guides.
•Screw tight the four screws on the underside of the housing.
Warning
Patient Safety — Choose cables and connectors with the appropriate voltage and current
carrying capacity.
Note
The RAB can be connected to the hospital alarm system in different ways, depending on whether or not the
power failure detection mode is configured and whether or not the hospital alarm system is using the
current monitoring mode.
Power failure detection mode ENABLED
•hospital alarm system using current monitoring mode: connect terminals REL 1 and REL 2
(break contact when power off/alarm)
•hospital alarm system not using current monitoring mode: connect terminals REL 2 and REL 3
(make contact when power off/alarm)
Power failure detection mode DISABLED
•hospital alarm system using current monitoring mode: connect terminals REL 2 and REL 3
(break contact when alarm )
•hospital alarm system not using current monitoring mode: connect terminals REL 1 and REL 2
(make contact when alarm)
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6.2 RAB Remote Light (RAB RL only) Connector
Figure 6.4 RAB RL Remote Light Connector
A 9 pin Sub-D connector to connect the EAGLE Remote Light 8500AAX to the RAB RL
Pinning of the 9-pin Sub-D connector:
VCC+12VDC from external medical power supply
GNDGND from external medical power supply
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6.4 Cabling RAB RL internal
Figure 6.6 RAB RL cabling
Wire 1 (red) is to be connected to REL2 and
Wire 2 (red/black) is to be connected according to the selected alarm mode:
• REL3 when operating with power failure detection (default mode) or
• REL1 when operating without power failure detection
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7 ASSEMBLY DRAWINGS
Introduction
Included in this section is a complete set of mechanical diagrams, Reference diagram and schematic
diagrams.
Spare Part List - These list shows the complete parts for service use.
Mechanical diagrams - These diagrams shows the mechanical assembly of RAB
and RAB RL
Reference diagrams - These diagrams shows provide a reference and view of the
used components in the schematic.
Schematic diagrams - These diagrams shows the electrical wired connections
between the used analog and digital electronics components.
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7.1 Spareparts
Electronic Parts
Part DescriptionDetailed Part DescriptionPart No.
Remote Alarm BoxRemote Alarm Box RAB (RAB Box
including Printed Circuit Board)
Remote Ala rm Box Remote
Light
Spare PCB. Remote Alarm
Box
Power SupplyPower Supply SW172 (12V)2000300-001
Assembly Remote LightAssembly Remote Light for RAB RL Box8500AAX
FuseFuse for Relay circuit 3.15A Slow Blow91208440
Remote Alarm Box Remote Light (RAB
RL Box including Printed Circuit Board)
Spare PCB. Remote Alarm Box for RAB
and RAB RL Alarm Boxes (High Pot
tested)
2005693-001
2005693-006
2007067-001
Mechanical Parts
Part DescriptionDetailed Part DescriptionPart No.
Optical Light GuideOptical Light Pipe for RAB, RAB RL2005478-001
Cable clampCable clamp for RAB91614100
Plastic nozzlePlastic nozzle for cable of RAB42103273
Cable clampCable clamp for RAB RL91618976
Bottom plateBottom plate metal for RAB RL2006575-001
Adapter plateAdapter plate metal for GCX mounting.2006576-001
Holder for Power SupplyMetal Holder for Power Supply SW1722006574-001
BracketMetal Bracket for Power Supply Holder2006573-001
Cables and Connectors
Part DescriptionDetailed Part DescriptionPart No.
Adapter Autoport to M-PortAdapter Autoport to M-Port2001973-001
Cable Assembly RJ45 5ftCable Assembly RJ45 to bedsides 5ft418335-001
Cable cord 2 wireCable cord 2 wire (has to be ordered in
meter)
91906200
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The following Power Cords are only used for RAB/RL units
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Marquette Hellige GmbH
Not equipped in Version :
x1
2004576-001
x2
x3
x4
x5
Revision-No
ER24685
MR27364
ECO-066622
REVISIONS
Index
1
A
B
Date / Name
03.11.00/WMW
20.12.00/TYR
16.03.01/TYR
A03
DRAWN
APPROVED
ISSUED
D-79007 Freiburg
2004575-001
Date / Name
03.11.00/WMW
03.11.00/SNA
W.Waltersberger
2004577-001
SCHEMATIC
INTFC NURSE CALL
Sheet:
11
of
$USER_CAD_B/2004575/design
[2000, 7, 19, 4]
gemedicalsystems.com
European Headquarters
GE Medical Systems
Information Technologies GmbH
Postfach 60 02 65
D-79032 Freiburg • Germany
T el. +49 761 45 43 - 0
Fax +49 761 45 43 - 233
World Headquarters
GE Medical Systems
Information Technologies, Inc.
8200 West T ower A venue
Milwaukee, WI 53223 • USA
T el . +1 414 355 5000
Fax +1 414 355 3790
Asia Pacific
GE Medical Systems Hong Kong Ltd.
11th Floor , The Lee Gardens
33 Hysan Avenue
Causeway Bay Hong Kong
Te l:+852.2100.6300
Fax:+852.2100.6292
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