This manual (810-0334-XX) applies only to 100-Series Monitors with serial numbers beginning with an “M” (such as
ME00204, or MB00223), and to printers with serial numbers beginning with MCO. If your printer’s serial number begins
with TCO, and your monitor’s serial number begins with TB, use Service Manual 810-0012-XX; if your monitor’s serial
number begins with TE, use Service Manual 810-0257-XX.
Model 102/LCD: 6515-01-3156196
Model 104/LCD: 6515-01-3156198
Model 106/LCD: 6515-01-3156197
Model 102/EL: 6515-01-3627449
Model 104/EL: 6515-01-3627451
Model 106/EL: 6515-01-3627447
Expansion Module with Printer: 6515-01-3159814
Oximeter (SpO2): 6515-01-3631219
Protocol® and Propaq® are registered trademarks of Protocol Systems, Inc.
Protocol Systems, Inc. is protected under various patents and patents pending.
NELLCOR® and DURASENSOR® are registered trademarks, and C-LOCK™ and
OXISENSOR™ are trademarks of Nellcor, Incorporated. Nellcor is protected under U.S.
patents 4,621,643, 4,653,498, 4,700,708, 4,770,179, 4,802,486, 4,869,254, 4,928,692, and
4,934,372.
HP and Hewlett-Packard are registered trademarks of Hewlett-Packard Company.
Protocol Systems, Inc.
8500 S. W. Creekside Place
Beaverton, OR 97005 USA
(503) 526-8500
Customer Service: (800) 289-2500
Facsimile: (503) 526-4300
Technical Service: (800) 289-2501
Part Number: 810-0334-01Rev. A
First Printing: 4/94
Printed in the U.S.A.
Service Manual Update/Change Information
A-Series Hardware
Service Manual Update
Introduction
The following table identifies important information about this update.
ItemInformation
This update/change has part number810-0698-00 Rev. A
This update/change affects/covers information
in manual(s) with Protocol part number(s)
This update/change affects/coversPropaq monitors with “A” serial number prefix
The information in this update/change is provided because of
For more information contactProtocol Systems, Inc. Technical Support at:
810-0334-01
New revision of hardware in Propaq monitor
prompted new serial number prefix “A” which
requires update/change to service information already published for existing Propaq
monitors.
800 289 2501 or 503 526 8500. See the
Service Manual for other access information.
The Flexible Monitoring Company
1 of 4
Copyright 1995 by Protocol Systems, Inc. All rights reserved. No part of this document may be
duplicated in any form without the written permission of Protocol Systems, Inc.
Propaq
, Acuity
, and Protocol
are registered trademarks of Protocol Systems, Inc.
Protocol Systems, Inc.
Technical Service Dept.
8500 SW Creekside Pl.
Beaverton, Oregon 97008-7107
In the United States: 800.289.2501
Worldwide: 503.526.8500
Facsimile: 503.526.4910
Worldwide e-mail: solutions@protocol.com
World Wide Web access: http://www.protocol.com/service
Overview
In 1994, Protocol Systems introduced the “International” series of Propaq monitors designated
with the serial number prefix “A.” This hardware reduces electromagnetic emissions, improves
susceptibility to electro-magnetic interference (EMI), and incorporates other features implemented
in the latest version of Propaq software, including the End-tidal CO
these changes, this Service Manual update was produced to inform you of the effects, if any, the
changes had upon current service manuals.
The information in this update/change is applicable only to the Propaq Service Manual part number 810-0334-01. It does not affect any other service document.
For board layouts, schematics, and assembly drawing changes effected with the release of A series
hardware, contact Protocol Systems for information.
Overview of Changes to Sections
monitoring option. Due to
2
Section AffectedDescription
Section 1None
Section 2None
Section 3None
Section 4None
Section 5None
Section 6None
Section 7None
Section 8Additional part numbers. Contact Protocol
Technical Support.
AppendicesNone
There are no other changes to the document identified above.
Protocol Systems, Inc.3 of 4
###
4 of 4 Service Manual Update
Propaq 100-Series MonitorsSafety Summary
Safety
Summary
CAUTION
WARNING
The general safety information in this summary is for both operating and
servicing personnel. Specific warnings and cautions will be found
throughout the Operator’s Guide and other manuals where they apply. Such
specific warnings and cautions may not appear here in this summary.
CAUTION statements in the documentation identify conditions or practices
that could result in damage to the equipment or other property.
WARNING statements in the documentation identify conditions or practices
that could result in personal injury.
Symbols The following symbols may appear in the documentation, and on labels on
the Propaq monitors.
DANGER: Risk of explosion when used in the presence of flammable
anesthetics. (This is on older versions only.)
Type CF, Isolated patient connections comply with the allowable risk
(leakage) current limits for direct cardiac application and are protected
against the effects of defibrillation.
Type BF, Isolated accessible and applied parts comply with the allowable
risk (leakage) current limits for noncardiac body applications, protecting the
patient and operator from risk of electric shock.
Protected against water dripping vertically. (Protection Classification IPX1
per IEC Publication 529.)
IPX1
DC power input connector for applications not requiring a “high output”
power adapter.
DC power input connector for applications requiring a “high output” power
adapter.
For continued fire protection, use only the specified fuse.
Internal power transformer meets requirements of a short-circuit-proof
safety-isolating power transformer (symbol is located on ac power adapter).
Caution: Refer to User’s Guide and accompanying documentation.
Caution: Refer servicing to qualified service personnel. (For products
certified by Underwriters Laboratories.)
Battery.
Positioning of battery.
Calibration/Maintenance Manual810-0334-01i
Safety SummaryPropaq 100-Series Monitors
Direct current.
Alternating current.
For indoor use only.
Important Safety
Considerations
Place the product in a location where it cannot harm the patient should it fall
from a shelf or other mount.
Do not autoclave this product.
Inspect the power adapter cord periodically for fraying or other damage, and
replace the adapter as needed. (The power adapter is not a serviceable part;
however, the detachable power cord used with the Universal Power Adapter
is replaceable). Do not operate the apparatus from mains power with a
damaged power adapter cord or plug.
Frequent electrical and visual checks should be made on cables and
electrode wires. Broken or frayed electrode wires, or loose snap-fittings may
cause interference or loss of signal. Particular attention should be paid to the
point at which the wire enters the snap-fittings, since flexure will eventually
cause breakage of strands at this point.
Avoid electrosurgery burns at monitoring sites by ensuring proper
connection of the electrosurgery return circuit. If the electrosurgery return
electrode is improperly connected, the other patient-connected monitoring
electrodes and transducers (particularly ECG electrodes and temperature
probes) will serve as return paths for the high-frequency energy. This is
especially true for older electrosurgery units which have the return circuit
deliberately earth-grounded. For improved safety, never deliberately ground
the return circuit of an isolated-output electrosurgery unit. If necessary,
operate the monitor on battery power only to prevent a return to earth
ground through the monitor.
To assure operator safety during defibrillation, keep the discharge paddles
away from ECG and other electrodes, as well as other conductive parts in
contact with the patient. During defibrillation, always avoid contact with any
accessories, such as cables and sensors, connected to the Propaq’s left side
panel. For additional safety precautions, refer to the defibrillator operator’s
manual.
To ensure patient safety, the conductive parts of the ECG electrodes
(including associated connectors) and other patient-applied parts should not
contact other conductive parts, including earth ground, at any time.
Do not operate this product in the presence of flammable anesthetics.
Explosion can result. This product must only be operated in strict
conformance with local fire prevention regulations.
ii810-0334-01Calibration/Maintenance Manual
Propaq 100-Series MonitorsSafety Summary
NOTE
Within certain governmental jurisdictions, all interconnected
accessory equipment must be labeled by an approved testing
laboratory. After interconnection with accessory equipment, risk
(leakage) current and grounding requirements m ust be maintained.
To ensure patient safety, use only accessories recommended or supplied by
Protocol Systems, Inc. For a list of those accessories, see the Protocol
Products and Accessories book (PN 810-0409-00) that accompanies the
Users Guide.
Do not autoclave accessories unless the manufacturer’s instructions clearly
approve it. Many accessories can be severely damaged by autoclaving.
To ensure conformance to risk (leakage) current requirements when
operating from an ac mains power source, use only a Protocol Systems’
503-0002, 503-0053, or 503-0054 power adapter.
Pour limiter le courant de fuite conformément aux exigences lorsque
l’appareil est branché au secteur, utiliser seulement un bloc d’alimentation
de la série 503-0002 503-0053, 503-0054.
A product that has been dropped or severely abused should be checked by
qualified service personnel to verify proper operation and acceptable risk
(leakage) current values.
While under warranty, the Propaq should be serviced only by Protocol
Systems’ service personnel. Service documentation is available from
Protocol Systems, Inc. to aid the biomedical engineer during post-warranty
period service.
Component replacement and internal adjustments must be made by qualified
service personnel only.
Calibration/Maintenance Manual810-0334-01iii
Section 1General Information
Available Documentation................................................................................................1-1
About This Manual .........................................................................................................1-1
The Calibration/Maintenance Manual contains information for the
service technician to service Propaq monitors at the replaceable modulelevel. Replaceable modules are items that can be easily replaced without
desoldering circuit board components.
Servicing to the component level requires the Schematics & DrawingsSet, and the appropriate option section for SpO
options.
− For detailed circuit descriptions, bills of materials, mechanical
assembly drawings, and schematics of the monitor main board,
interconnect board, and recharger board, see the Schematics &Drawings Set (orderable separately as 810-0334-10).
− Similar information on the Printer, Oximeter, and Capnograph is
found in the appropriate option section of the Schematics &
Drawings Set:
Service manuals contain service information for the biomedical electronic
technician (BMET or CBET). Only factory-trained technicians should
service the Propaq series monitors.
NOTE
,CO2andPropaqPrinter
2
This manual does not include operating instructions or
information. Refer to the appropriate user's guide.
About This
Manual
Calibration/Maintenance Manual810-0334-011-1
The Calibration/Maintenance Manual contains eight sections and three
appendices, as described below.
•
Section 1 General InformationThis section contains information
about how to use the manuals, and a description of the Propaq series
monitors, optional Expansion Module with printer, SpO
option.
CO
2
•
Section 2 Installation and ServiceThis section contains instructions
on how to unpack and repack the monitor for shipping. Servicing
interval recommendations are provided for developing preventive
maintenance schedules. A functional verification procedure allows
checking the performance and safety features of the monitor without
opening the case.
•
Section 3 Calibration—This section lists all tools and test equipment
needed to perform a complete calibration procedure. A description of
the Service Menu functions is provided. The calibration procedure
allows you to calibrate the Propaq to factory specifications.
•
Section 4 Troubleshooting—This section contains descriptions of
screen messages and software error codes for use in troubleshooting.
•
Section 5 Replacement Procedures—This section contains information
and step-by-step instructions on making modular repairs to the Propaq,
and shows you how to remove and replace serviceable modules.
•
Section 6 Theory of Operation—This section describes the Propaq’s
circuitry at the system and functional-block levels only.
Detailed circuit operation descriptions for each of the monitor’s circuit
boards and specific options are contained in the Schematics & DrawingsSet and appropriate option section, as noted on the previous page.
•
Section 7 Diagrams—This section contains block diagrams and cabling
drawings.
•
Section 8 Replaceable Parts—This section lists serviceable mechanical
and electrical parts (generally in kit form) for the Propaq series
monitors, the printer, the pulse oximeter, and the capnography option.
•
Appendix A Buildable Test Equipment—This section provides
descriptions and schematics for test equipment that you can build for
servicing the Propaq.
•
Appendix B Dynatech/Nevada Patient Simulator Modification—This
section shows you how to modify Dynatech/Nevada models 213A,
215A, and 217A Patient Simulators for use with the Propaq series
monitors. This section is especially important if you simultaneously
connect both the ECG and invasive blood pressure channels of this
patient simulator to the Propaq.
•
Appendix C Software Revision History—This section lists the
software revisions for the Propaq.
Product
Description
The Propaq series is a product line of lightweight, ultra-portable patient
monitors applicable to a wide variety of health care services. These
monitors measure and display a patient’s vital signs, including ECG,
non-invasive blood pressure, invasive blood pressure, temperature,
oxygen saturation derived by pulse oximetry (with SpO
mainstream carbon-dioxide monitoring (w ith CO
Option). Propaq
2
Option) and
2
configurations vary depending on the model. Table 1-1 lists the monitors
and their configurations available at the printing of this manual.
1-2810-0334-01Calibration/Maintenance Manual
Propaq 100-Series MonitorsSection 1—General Information
All models of monitor may be ordered with the optional Hewlett-Packard
patient connector side panel.
The Propaq Expansion Module allows SpO
and CO2monitoring to be
2
added to any Propaq monitor. The Expansion Module with Printer (EMP)
includes a high-resolution, dot-matrix printer for documenting patient
vital signs.
The Propaq 100-Series Monitors are sold by Protocol Systems, Inc.
under the w arranties set forth in the warranty statement supplied with
each product. Additional copies of the w arranty statement can be
obtained from Protocol Systems, Inc.
Propaq manuals are updated with each new monitor design, and history
information is provided (as deemed appropriate) for earlier monitors. In
some cases, an early manual is re-released with an updated part number;
in other cases, a new manual is released. The following table lists the
releases of Propaq manuals, and cross-references the serial numbers of
the monitor and printer (and the software version number) to which the
manual applies.
Updates for software 4.xx.xxx,
misc. correction and update
data, and international
certification
9/90Updates for software 5.xx.xxx,
adding SpO
2
6/91Updates for software 6.0,
includes printer operator’s
guide, and SpO
.AddsEL
2
option.
8/91Hewlett-Packard Connector
update, supplements 810-0035-02
10/91Pulse oximetry update,
supplements 810-0035-02
6/92Software 6.2 update,
supplements 810-0035-02
6/92Software 7.0 update,
supplements 810-0035-02
4/93Software version 8.0. Original
release of User’s Guide. English
language
1-4810-0334-01Calibration/Maintenance Manual
Section 2
Installation and Service
IntroductionThis section provides the information for unpacking, initial setup and
checkout of the Propaq 100-series monitors. Information is provided for
developing a preventive maintenance schedule.
When the monitor is first unpacked and before it is placed in service, the
functional verification and safety checks provided in this section should be
performed.
Unpacking/
Repacking
W arranty
Service
Use the following guidelines when unpacking the monitor from its shipping
carton.
1. Before unpacking the monitor, check the shipping carton for damage.
2. If damage is apparent, it is a good idea to stop unpacking the carton and
contact the shipping company for further instructions. If the carton is
intact, unpack the Propaq.
3. With the Propaq out of its carton, check to see that all the items listed on
the Packing Slip (provided with shipment) are in the shipping carton.
4. If an item is missing, first recheck the carton, then check with your
receiving department. If necessary, contact Protocol Systems, Inc. at the
address and phone number shown in Repair and Upgrade Support.
The shipping carton and packing material should be saved for
repacking the monitor in case it needs to be sent to a repair center
or back to Protocol Systems for service.
If during the warranty period, the Propaq requires service, DO NOT
ATTEMPT TO SERVICE IT YOURSELF. For fast, convenient service from
Protocol Systems, follow the procedure below.
Calibration/Maintenance Manual810-0334-012-1
Section 2—Installation and ServicePropaq 100-Series Monitors
Repair and
Upgrade
Support
For repair and upgrade information, contact:
Technical Services Dept.
Protocol Systems, Inc.
8500 S. W. Creekside Place
Beaverton, OR 97005-7107 U.S.A.
or call Protocol Systems, Inc. in the U.S.A. at (800) 289-2500.
Technical Services toll-free number: (800) 289-2501.
For world-wide facsimile communications, call (503) 526-4200.
If calling from outside the United States, call (503) 526-8500.
When calling Protocol for service information or to order service parts,
please have the following information ready:
•
model number (102, 104, or 106 from front of monitor),
•
serial number (from back of instrument),
•
software version (from startup screen)
•
attached options, if any (such as printer or SpO2option)
•
a full description of the problem or service needed
•
your complete return shipping address
•
your purchase order number (for non-warranty repairs, all upgrades
and parts orders)
•
a contact name and phone number for any further questions.
Model and serial numbers are printed on the label located on the rear of the
monitor and options. The software version number is displayed each time
the monitor is powered on.
If you are returning a Propaq for service:
•
The Technical Service representative will give you a Return Material
Authorization (RMA ) number and tell you w here and how to ship the
monitor for service. Without the RMA number, Protocol cannot accept
the monitor for service.
•
Package the monitor in its original shipping carton using the original
packing material. The material and carton w ere specifically designed
for the monitor’s safety during shipment.
•
Clearly address the box and ship it to the address provided by
Protocol’s Technical Service representative. Be sure to write the RMA
number on the outside of the shipping carton, and on any included
correspondence.
For the location of your nearest Protocol Systems authorized repair center,
or for information on all Protocol Systems products, contact Protocol
Systems, Inc.
2-2810-0334-01Calibration/Maintenance Manual
Propaq 100-Series MonitorsSection 2—Installation and Service
Recommended
Service
The Calibration/Maintenance Manual provides instructions and information
for technicians to repair the Propaq at the replaceable module level.
Replaceable modules include circuit boards, large hardware items, such as
the air pump, check valve, chassis parts, and other parts easily replaced
without desoldering of surface-mount components and other small hardware.
Module-level repair allows monitor repair in minimal time and for a
nominal price for the replaceable module.
Because of the specialized equipment and knowledge required to
manufacture and repair the Propaq, Protocol Systems, Inc. recommends that
only Protocol’s authorized repair facilities provide component-level repair. If
repair by other than Protocol’s authorized repair facilities is required, such a
facility must have the necessary equipment to service and repair surface
mount technology (SMT) electronics as well as the specialized equipment to
service Propaq monitors. The Schematics & Drawings Set (orderable as
810-0334-10) and appropriate option section (SpO
PN 810-0334-30, or CO
PN 810-0334-40) provides schematics, parts lists,
2
PN 810-0334-20, Printer
2
etc. helpful in component-level servicing. Contact Protocol Systems, Inc. for
more information.
Service IntervalsTable 2-1 lists recommended service intervals and procedures that should be
considered in order to keep the monitor in good operating condition.
Table 2-1. Recommended Service Intervals/Procedures
Interval/ConditionPerform
Semi-annuallyComplete Functional Verification and
Safety Check (Section 2).
Minimum every three yearsReplace lithium battery. Replace battery
pack. Replace air filter.
Monitor is dropped, in an accident, or
suspected rough handling.
Suspected malfunction with all or part
of functions.
Monitor fails Functional Verification.Repair followed by Functional
Module has been replaced and monitor
fails Functional Verification.
Every 5,000 hours of operation or
whenever screen becomes difficult to
view
Complete Functional Verification and
Safety Check (Section 2).
Functional Verification (Section 2) of
suspected function(s).
Verification (Section 2), and Calibration
as required (Section 3).
Repair followed by Functional
Verification (Section 2), and Calibration
as required (Section 3).
Replace LCD backlight (LCD monitors
only)
Calibration/Maintenance Manual810-0334-012-3
Section 2—Installation and ServicePropaq 100-Series Monitors
Functional
V erification
The functional verification procedures verify proper operation of the
monitor, oximeter, and printer. This procedure should be performed at
intervals or conditions listed in Table 2-1.
Self TestMany functions, such as alarms, waveform and scale sizing, and printer
control, are software operations. Since system software is automatically
checked during the monitor’s power-up self-test, all software functions work
normally if no error messages appear during the power-up sequence. (Some
error messages indicate hardware failures.)
The Service Menus Service Menus are provided to facilitate functional verification. The Service
Menus (Figure 2-1) contain several functions for testing and verifying the
Cuff channel, display, invasive pressure channel (models 104 and 106 only),
and printer. During the functional verification procedure, the Service Menu
functions will be accessed to perform necessary tests.
SENSORSFREEZESYSTEMDISPLAYALARMS
PRINTERMAIN MENUMORENET OFFPROGRAM
INSERVMAIN MENUMORETIME/DAYSERVICE
CUFF TSTMAIN MENUMORESPO2 TEST
LOOP TESTMAIN MENUOUT TEST
CYCLEMAIN MENUBORDERCOLUMN 2COLUMN 1
PUMP TSTMAIN MENUCUFF CALAUTO PMP
a
IBP TEST applicable only for Propaq 104, 106.
b
SPO2 TEST intended for factory use with SpO2 option.
c
NET TEST applicable only for Network option.
IBP TEST
PIXL TST
a
Fig. 2-1. The Service Menus, Version 7
b
c
MAIN MENUMORENET TEST
VERSION 7.x
2-4810-0334-01Calibration/Maintenance Manual
Propaq 100-Series MonitorsSection 2—Installation and Service
SENSORSFREEZESYSTEMDISPLAYALARMS
d
SNAPSHOT
INSERVMAIN MENUMORETIME/DAYPROGRAM
CHANGEMAIN MENUMORESERVICENEXT
CUFF TSTMAIN MENUMORESPO2 TEST
TEMP TESTMAIN MENUMORENET TEST
CO2 TEST
LOOP TESTMAIN MENUOUT TEST
CYCLEMAIN MENUBORDERCOLUMN 2COLUMN 1
e
IBP TEST
PIXL TST
d
a
MAIN MENUMORENET OFFPRINTER
b
c
MAIN MENUMORE
PUMP TSTMAIN MENUCUFF CALAUTO PMP
a
IBP TEST applicable only for Propaq 104, 106.
b
SPO2 TEST intended for factory use with SpO2 option.
c
NET TEST applicable only for Network option.
d
Depends on option installed.
e
Applicable only for CO2option.
Fig. 2-2. The Service Menus, Version 8
VERSION 8.x
Menu functions are accessed by pressing one or a series of buttons below
menu labels on the monitor display. Button presses to access any function in
the Propaq are shown in this manual with the > character separating the
names of the buttons to be pressed. For example, SENSORS > ECG >
LEAD means starting from the Main Menu, press the SENSORS button,
then the ECG button, and finally the LEAD button.
The Service Menu is activated by pressing from the Main Menu (Version
7.x software) SYSTEM > MORE > SERVICE, or (Version 8.x software)
SYSTEM > MORE > MORE > SERVICE.
NOTE
In the following procedures, where Version 8.x button presses differ
from Version 7.x button presses, both versions are given. Otherwise,
button presses are the same for both versions.
Calibration/Maintenance Manual810-0334-012-5
Section 2—Installation and ServicePropaq 100-Series Monitors
Equipment Required Table 2-2 lists all the equipment needed to perform a functional verification.
Some equipment can be manufactured. See Appendix A for information on
manufacturable test equipment.
Table 2-2. Equipment Required for Functional Verification
Equipment Description
Mercury-column Manometer with Bulb (400 mmHg), Baumanometer 14-383 wall
mount Manometer or equivalent
50 MHz Triggered Sweep Oscilloscope, Tektronix 2225 or equivalent
Variable DC Power Supply, 0-36 V, 3A, VIZ WP-715A or equivalent
Patient Simulators, Dynatech/Nevada 213A, 215A, or 217A with Temperature and
EGG Cable/Leads
Electromedics 37° C Temperature Sensor Simulator (See Appendix A)
IBP Simulator, 5 µV/mmHg/volt, Fogg Systems BP48C, BP28, or MDE Datasim
6000 with IBP cables
Adult Cuff Kit, Protocol PN 008-0006-XX
Protocol Cuff Calibration Kit, Protocol PN 008-0012-XX
Power Supply Adapter Cables (See Appendix A)
Propaq AC Power Adapter
Safety Analyzer, Dynatech/Nevada (formerly Neurodyne-Dempsey), 431F-1D or
equivalent
Rod-L Model M100AVS5 High-Voltage Potential Tester, or equivalent
NELLCOR Pocket Tester, PT-2500
Test gas source: dry 4% to 10%* CO
Tw o rubber test tube stoppers, with 1/8" to 1/4" vent holes opened through (for
CO
tests)
2
*Gas may be between 4 and 10%, but exact CO2concentration must be certified within
±0.01%. See procedure later in this section for determining partial pressure.
, balance air (with flow meter)
2
ProcedureNOTE
If the monitor has been stored for longer than one month
without the monitor connected to the ac adapter (for
recharging), the battery voltage should be checked. The battery
may need to be replaced if it cannot hold a charge.
The functional verification must be done only when the monitor is fully
assembled. Equipment required to perform this procedure is shown in Table
2-2. Most items not commercially available can be made according to the
information in Appendix A.
2-6810-0334-01Calibration/Maintenance Manual
Propaq 100-Series MonitorsSection 2—Installation and Service
NOTE
If you plan to use a Dynatech/Nevada model 213A, 215A, or 217A
Patient Simulator to simultaneously simulate ECG and invasive
blood pressure, see Appendix B for important information.
If the monitor did not pass the functional verification, or when it is time to
do a routine calibration, see the Calibration Procedure in Section 3.
Functional verification and safety checks must always be done after monitor
disassembly or calibration, or whenever there is a question about the safety
of the patient functions.
NOTE
Before starting the verification procedures, charge the battery
for at least 8 hours with the monitor turned off. (Charge for 12
hours if a Printer or SpO
module is attached.)
2
Power SystemThe following steps check the integrity of the power system.
1. If the ac power adapter is not plugged in, plug it into an ac socket
with the correct voltage and connect it to the monitor’s right side panel
dc power connector.
2. Check that the green
BATTERY CHARGING indicator lights.
3. Disconnect the power adapter from the monitor. Check that the
BATTERY CHARGING indicator turns off.
CAUTION
In the next steps, carefully check for the proper polarity of the
connection between the power supply and the monitor. If voltage
is applied with the wrong polarity, it will blow an internal fuse
(F1 on the Recharger board). Refer to the diagram on the
monitor’s right side panel for proper polarity.
4. Turn on the dc power supply and set it for 15 V
5. Using the power supply adapter cable (constructed as shown in
Appendix A), connect the power supply to the monitor’s dc input
connector on the right side panel.
6. Check that the
BATTERY CHARGING LED indicator lights.
7. Check that the current draw from the supply is less than 650 mA.
NOTE
Initial charge current can be as high as 880 mA. However, as the
battery charges, the current will decrease. A fully charged battery
draws less than 100 mA. You should notice the current draw slowly
drop the longer the dc supply is connected to the monitor.
±0.5 V.
8. Turn off the power supply.
9. Disconnect the supply from the monitor.
Calibration/Maintenance Manual810-0334-012-7
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