Manu Usu Oper Manto Monit Procare 300 Dinamap

DINAMAP® ProCare Monitor
Service Manual
This manual is for DINAMAP ProCare Monitors models 100, 200, 300, and
400, with or without printers.
• ProCare 100: BP, Pulse

• ProCare 200: BP, Pulse, and Temp
• ProCare 300: BP, Pulse, and SpO2
• ProCare 400: BP, Pulse, Temp, and SpO2
The model of the Monitor determines which parameters are in your monitor.
Please refer to applicable sections.
Reissues and Updates

Changes occurring between issues are addressed through Change
Information Sheets, Addendums, and replacement pages. If a Change
Information Sheet does not accompany this manual, it is correct as printed.
Errors and Omissions

If errors or omissions are found in this manual, please notify:
GE Medical Systems Information Technologies
Technical Publications
4502 Woodland Corporate Boulevard
Tampa, FL 33614
1-877-274-8456
Part No. 2009381-001 A
The content of this document including all figures and drawings is proprietary
information of GE Medical Systems Information Technologies, provided
solely for purposes of operation, maintenance or repair, and dissemination
for other purposes or copying thereof is prohibited without prior written
consent by GE Medical Systems Information Technologies, Tampa, Florida.
Illustrations may show design models; production units may incorporate

changes.
Hierarchy of Warnings and Cautions

A general warning is a statement that alerts the user to the possibility of
injury, death, or other serious adverse reactions associated with the misuse
of the device. A warning relates to steps in a procedure.
A general caution is a statement that alerts the user to the possibility of a

problem with the device associated with its use or misuse. Such problems
include device malfunction, device failure, damage to the device or damage
to other property. A caution relates to steps in a procedure.
© GE Medical Systems Information Technologies 2002, TAMPA, FL 33614
Printed in the U.S.A. All rights reserved.
Revision A ProCare Patient Monitor Service Manual

2009381-001
World Headquarters
GE Medical Systems
Information Technologies, Inc.
8200 West Tower Avenue
Milwaukee, WI 53223 USA
Tel:•+ 1 414 355 5000
•1 800 558 5120 (US only)
Fax:•+ 1 414 355 3790
European Representative
GE Medical Systems
Information Technologies GmbH
Munzinger Straße 3-5
D-79111 Freiburg
Germany
Tel: •+ 49 761 45 43 - 0
Fax: •+ 49 761 45 43 - 233
Asia Headquarters
GE Medical Systems
Information Technologies Asia; GE (China) Co., Ltd.
24th Floor, Shanghai MAXDO Center,
8 Xing Yi Road, Hong Qiao Development Zone
Shanghai 200336, P.R. China
Tel: •+ 86 21 5257 4650
Fax: •+ 86 21 5208 2008
ProCare Patient Monitor Service Manual Revision A

2009381-001
DINAMAP®
ProCare Monitor
Service Manual
2009381-001 Revision A
NOTE: The information in this manual only applies to ProCare Monitor. It does not apply to earlier Monitors. Due to
continuing product innovation, specifications in this manual are subject to change without notice.
© GE Medical Systems Information Technologies, 2002. All rights reserved.
T-2 ProCare Monitor Revision A

2009381-001
Table of Contents
1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1.1 Scope of Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
1.2 Manual Changes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
1.3 Service Policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

1.3.1 Service Contracts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1.3.2 Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1.3.3 Return to Factory Repair Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1.3.4 Service Loaners . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
1.3.5 Repair Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
1.3.6 Replacement Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
1.4 Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

1.4.1 General Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
2 Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
2.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
2.2. Product Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
2.3. Controls, Indicators, and Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

2.3.1. ProCare Monitor Rear Panel Connections . . . . . . . . . . . . . . . . . . . . . . . 4
2.3.2. Front Panel Controls and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
2.4. Host Communications Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

2.4.1. DB15 Connector Pin Assignments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
2.5. Compatible Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
2.6. Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
3 Principles of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
3.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
3.2 Overall Principles of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

3.2.1 SpO2 (Model 300 and 400) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Revsion A ProCare Patient Monitor Service Manual

2009381-001
Table of Contents
3.2.2 Cuff Blood Pressure (BP) and Pulse . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

3.2.3 Temperature (Model 200 and 400) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
3.2.4 Host Communication Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
3.3 Functional Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

3.3.1 Main Board PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
3.3.2 User Interface (UI) Board PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
3.3.3 SPO2 PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
3.3.4 Printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
3.3.5 Pneumatic Valve/Manifold (PVM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
3.3.6 Optical Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
4 Calibration & Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . 1

4.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
4.2 Configuring Your ProCare Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

4.2.1 Unpacking and Preparation for Installation . . . . . . . . . . . . . . . . . . . . . . . 4
4.2.2 Set the Date and the Clock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
4.2.3 Parameter Level Functional Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
4.3 Periodic Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

4.3.1 As Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
4.3.2 Annual Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
4.4 Care of the Storage Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

4.4.1 Battery Charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
4.5 Safety Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

Notes on Electrical Safety Testing of the ProCare Monitor: . . . . . . . 9
4.5.1 Temp Circuit Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
4.5.2 SpO2 Circuit Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
4.6 ProCare Patient Monitor Parameter Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

4.6.1 SETUP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
4.6.2 Leakage Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
4.6.3 Pressure Transducer Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
4.6.4 Pressure Transducer Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
4.6.5 Overpressure Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
4.6.6 Button Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
4.6.7 LED Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
4.6.8 External DC Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
4.6.9 NIBP Determination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
4.6.10 NIBP Overpressure Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

2009381-001
Table of Contents
4.6.11 Temperature (Perform if equipped with Temp module) . . . . . . . . . . . 16

4.6.12 SpO2 (Perform only if equipped with SpO2 module) . . . . . . . . . . . . . 17
4.6.13 Printer Output Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
4.6.14 Communication Port Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
4.7 Alarm Code Interpretation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

4.7.1 System Failures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Appendix A - Test Results Form . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Appendix B - Connectivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Appendix C - Display Cover: Removal, Installation . . . . . . . . . . . . . . . . . . . . . . . . . 25
Appendix D: Replacement Parts and Assemblies . . . . . . . . . . . . . . . . . . . . . . . . . . 27
5 Assembly Drawings & ProCare Schematics
Revsion A ProCare Patient Monitor Service Manual

2009381-001
Table of Contents

2009381-001
1 Introduction
Revision A ProCare Patient Monitor Service Manual 1-1

2009381-001
1-2 ProCare Patient Monitor Service Manual Revision A
2009381-001
1.1 Scope of Manual
This Service Manual provides service and parts repair information about the
DINAMAP ProCare Monitor. This manual is intended for use by trained
service technicians who are familiar with electromechanical devices and
analog circuit techniques.
WARNING
To reduce the risk of electric shock, do not

remove cover or back of any component.
Refer servicing to qualified service personnel.
Only qualified technicians should perform repairs to this equipment.
For information about operating the Monitor in a clinical environment, refer to

the separate Operations Manual.
This Service Manual consists of the following five sections:
Section 1 describes this volume and tells you how to use it. Information is
also provided about the physical and functional characteristics of the
Monitor, and how to get assistance in the event the unit fails to function
properly.
Section 2 provides a general overview of the ProCare Monitor including the

user controls, external connections and product/parameter specification.
Section 3 presents principles of operation for the Monitor, including an

overall system description and principles of operation at the component
level.
Section 4 provides information about periodic and corrective maintenance of

the Monitor and part list, replacement part lists. Procedures include module
performance testing, and calibration procedures. Information is also
provided to facilitate isolating faults to the subassembly level.
Section 5 provides component information about the Monitor, including

assembly drawings and electrical schematics.

2009381-001
Introduction: 1.2 Manual Changes
1.2 Manual Changes

If, in the normal course of using this manual, you notice errors, omissions,
incorrect data, or if you can suggest comments that may help improve this
manual, please send suggestion to:
General Electric Medical Systems Information Technologies

Technical Publications
4502 Woodland Corporate Boulevard
Tampa, Florida, 33614
Changes to the Service Manual, either in response to user input or to reflect

continuing product improvements, are accomplished through reissue.
Changes occurring between reissues are addressed through Change

Information Sheets and replacement pages. If a Change Information Sheet
does not accompany your manual, the manual is correct as printed.

2009381-001
Introduction: 1.3 Service Policy
1.3 Service Policy

The warranty for this product is two years Parts and Labor. In the event of a
monitor malfunction the monitor must be returned to General Electric
Medical Systems Information Technologies to be covered under warranty.
All repairs on products under warranty must be performed or approved by
Product Service personnel. Unauthorized repairs will void the warranty. Only
qualified electronics service personnel should repair products not covered by
warranty.
1.3.1 Service Contracts

Service contracts may be purchased on most products. Contact your Sales
Representative for details and pricing.
1.3.2 Assistance
If the product fails to function properly, or if assistance, service or spare
parts are required, contact Customer Support. Before contacting Customer
Support, it is helpful to attempt to duplicate the problem and to check all
accessories to ensure that they are not the cause of the problem. If you are
unable to resolve the problem after checking these items, contact General
Electric Medical Systems Information Technologies at 1-877-274-8456.
Prior to calling, please be prepared to provide:
product name and model number

a complete description of the problem
If repair parts or service are necessary, you will also be asked to provide:
the product serial number

the facility's complete name and address
a purchase order number if the product is in need of non-warranty repair
or to order spare parts
the facility's General Electric Medical Systems Information Technologies
account number
the appropriate part number for spare or replacement parts
1.3.3 Return to Factory Repair Service

If your product requires warranty, extended warranty or non-warranty repair
service, call Customer Support and a representative will assist you.
Estimates for non-warranty repairs are provided pre-set flat rates to facilitate
prompt service. In cases where the product has external chassis or case
damage, please advise the Customer Support representative when you call.
The Customer Support representative will record all necessary information

and will provide you with a Return Merchandise Authorization Number
(RMA). Prior to returning any product for repair, you must have a RMA
number.
Revsion A ProCare Patient Monitor Service Manual 1-5

2009381-001
Contact General Electric Medical Systems Information Technologies at

1-877-274-8456 Monday through Friday, 8:00 a.m. to 6:00 p.m. EST,
excluding holidays.
Packing Instructions
Follow these recommended packing instructions.
Remove all hoses, cables, sensors, and power cords from the monitor
before packing.
Pack only the accessories you are requested to return; place them in a
separate bag and insert the bag and the product inside the shipping
carton.
Use the original shipping carton and packing materials, if available.
If the original shipping carton is not available:
Place the product in a plastic bag and tie or tape the bag to prevent
loose particles or materials from entering openings such as hose ports.
Use a sturdy corrugated container to ship the product.
Pack with 4 to 6 in. of padding on all sides of the product.
Tape securely to seal the container for shipping.
Insurance
Insurance is at the customer's discretion. The shipper must initiate claims for
damage to the product incurred during shipping. Shipping damage is not
covered under warranty.
1.3.4 Service Loaners

Loaner units can be provided at no charge during the warranty period if your
product needs to be returned for factory service. If requested, loaner units
will be shipped within 48 hours to your facility. General Electric Medical
Systems Information Technologies will pay outgoing charges for a loaner
sent for product repairs under warranty.
The customer is responsible for shipping charges to return the loaner unit to
General Electric Medical Systems Information Technologies. All loaner units
must be returned within 5 business days after receipt of your repaired unit.
Loaner and/or Rental products are available to meet your needs in non-
warranty situations.
1.3.5 Repair Parts

Repair parts can be ordered from General Electric Medical Systems
Information Technologies:
Via phone: 1-877-274-8456, or Via FAX: 1-800-421-6841
Exchange replacement assemblies such as Circuit Board Assemblies are

also available; ask your Customer Support representative for details.

2009381-001
Most orders ship on the same day if received before 3PM Eastern Time.
Overnight freight options are available to meet your critical needs.
All orders must include the following information:
Facility's complete name, address, and phone number

FAX number
Your purchase order number
Your General Electric Medical Systems Information Technologies
account number (if available)
1.3.6 Replacement Accessories

Replacements such as hoses, sensors, etc. must be purchased from
General Electric Medical Systems Information Technologies at 1-800-558-
5102. Please have the Product Code of the item you wish to order, your
purchase order and account number available.

2009381-001
Introduction: 1.4 Product Description
1.4 Product Description

The Monitor is described below. Refer to Table 1-1 for specifications.
1.4.1 General Description

The ProCare Monitor provides a small, portable, easy-to-use monitoring
alternative for sub-acute hospital and non-hospital settings. The DC-
operated Monitor offers noninvasive determination of systolic blood
pressure, diastolic blood pressure, mean arterial pressure, pulse rate,
oxygen saturation, and temperature. Monitors are available with or without
integrated printers. ProCare Monitors are intended for use in various
markets, from the physician’s office to sub-acute triage and medical/surgical
units.
Indicators for external DC operation (from AC mains), battery operation, and

battery charging are at the front of the unit.
At the time of publication, the available functioning parameters included the

following:
NIBP
Nellcor™ Pulse oximetry (SpO2)
Masimo Pulse oximetry (SpO2)
Alaris™ Oral and Rectal thermometry
thermal recorder/printer
Other DINAMAP ProCare features include:
The ability to uses industry standard accessories

Remote alarm capability
Function keys for quick access to Alarm Silence, Monitor Menus, Print
and NIBP Inflate/Stop
The ProCare Monitor operates from either an external DC power supply, or

from the internal lead-acid storage battery. When external DC power
becomes available, the system rapidly switches from battery power to
external power.

2009381-001

2009381-001

2009381-001
2 Product Description
Revsion A ProCare Partient Monitor Service Manual 2-1

2009381-001
For your notes
2-2 ProCare Partient Monitor Service Manual Revision A

2009381-001
Product Description: 2.1 Introduction
2.1 Introduction
DINAMAP ProCare Monitors provide non-invasive determination of systolic
blood pressure, diastolic blood pressure, mean arterial pressure, pulse rate,
temperature, and oxygen saturation.
2.2. Product Configurations

Each ProCare Monitor is supplied with an accessory pack. The contents of
the pack vary according to model. Unpack the items carefully, and check
them against the checklists enclosed within the accessory boxes. If an
accessory is missing or if an item is in a nonworking condition, contact
General Electric Medical Systems Information Technologies Customer
Service immediately.
It is recommended that all the packaging be retained, in case the ProCare

Monitor must be returned for service in the future.
Revision A ProCare Partient Monitor Service Manual 2-3

2009381-001
Product Description: 2.3. Controls, Indicators, and Connectors
2.3. Controls, Indicators, and Connectors

Descriptions of the items shown are listed on the pages that follow. For
symbol definitions, refer to page 2-8 of this section.
2.3.1. ProCare Monitor Rear Panel Connections
1 Speaker Grille.
2 Data interface connector: Host communications port (15 pin D-type RS-
232 serial port) for use only with equipment conforming to IEC 601-1,
configured to comply with IEC 601-1.
3 Printer Door (optional.)

2009381-001
2.3.2. Front Panel Controls and Indicators
Buttons
1 Silence button: Press to mute audible alarms. Any alarm active that is
acknowledgeable is also removed whenever this key is pressed. When
pressed after alarm sounds (silence active), the silence icon (bell) lights
to indicate that audible alarms have been silenced for 2 minutes.
2 Alarms button: Press to view or adjust parameter alarm settings
3 +/- button (Plus/Minus): Press the + button to increment an adjustable
setting and the - button to decrement an adjustable setting. This button is
active only when a user-setting mode (limit or menu) is active.
4 Menu button: Press to access menu settings that can be adjusted while in
clinical mode (i.e., ALARM VOLUME, PULSE VOLUME, INFLATE
PRESSURE; refer to Operating Modes in this section for a description of
clinical mode.)
5 SpO2 sensor connector: SpO2 sensor cable attaches here .
6 BP connector: BP cuff hose attaches here.
7 Inflate/Stop button: Press to start a manual BP determination or stop any
BP determination.
8 Temperature probe holster: Temperature probe is stored here.
9 Cycle button: Press to start Auto Cycle or STAT mode.
10 Temperature probe cover storage: Box of probe covers is stored here
11 History button: Press to activate the history mode. When activated, it
displays the most recent entries stored. Press and hold the button for 2
seconds to clear all entries stored.
12 Print button: Press to print currently displayed values or all stored entries
when in history mode.
13 On/Off button: Controls on/off state of monitor; push for power on and
push again for power off.
14 Temperature probe connector: Temperature probe cable attaches here.

2009381-001
Front Panel
15 Silence icon: when Silence button is pressed after alarm sounds (silence
active), silence icon (bell) lights to indicate that audible alarms have been
silenced for 2 minutes.
16 Systolic window: 3-digit red LED indicates measured systolic Blood
Pressure in mmHg.
17 Diastolic window: 3-digit red LED indicates measured diastolic Blood
Pressure in mmHg.
18 Alarm volume indicator: lights to indicate you are making a change to the
alarm volume.
19 Pulse volume: illuminates to indicate you are making a change to the
pulse volume.
20 Inflate pressure: illuminates to indicate you are making a change to the
inflation pressure.
21 Pulse Rate window: 3-digit yellow LED shows the pulse rate in beats per
minute.
22 SpO2 pulse indicator: Red LED bar flashes to indicate that real-time pulse
rate measurements are being derived from SpO2 signals.
23 SpO2 window: 3-digit red LED indicates oxygen saturation in %.
24 MAP/Cuff window: 3-digit red LED indicates measured MAP in mmHg
and shows instantaneous cuff pressure during BP determination.
25 Min window: Displays the BP mode if manual or STAT is the cycle time
when in Auto Cycle mode.
26 Battery power indicator: Green LED indicates the Monitor is operating on
battery power.
27 Low battery power indicator: Yellow LED indicates LOW charge status of
internal battery.
28 Charging indicator: Green LED indicates presence of external power
source and battery charging.
29 Temperature window: 4-digit red LED indicates measured temperature.

2009381-001
Right-Side Panel
30 External power socket: To be used with approved GE Medical Systems
Information Technologies AC-DC power converter ONLY.

2009381-001
Symbols
The following symbols are associated with the ProCare Monitor.
Note: The model of the Monitor determines which symbols appear on it.
Attention, consult accompanying documents
Silence
Alarms
+/-
Menu
Inflate/Stop
Cycle
History
Print
On/Off
Battery Power
External Communications Port Connector
Charging
Defibrillator-proof type BF equipment
Class II equipment according to IEC 60536
Packaging label depicting the transportation and storage

atmospheric pressure range of 500 to 1060 hPa.

2009381-001
Product Description: 2.4. Host Communications Connector
2.4. Host Communications Connector

All host port signals are NON-ISOLATED and should be connected to
equipment conforming to IEC 601-1 ONLY. Where isolation of data
communication is required, the isolated level converter should be used. If
external alarm control is required, p/n 487208 (Isolated Remote Alarm Cable
Assembly) should ALWAYS be used. Please refer to the Information Sheet
included with the isolated remote alarm cable for operational details.
Note: When using remote alarm, the ProCare Monitor should be considered
the primary alarm source. The secondary alarm is used for secondary
purposes only.
2.4.1. DB15 Connector Pin Assignments

Connection Details
Host Port Connector (rear panel)
WARNING! Auxiliary equipment

connected to the DINAMAP® ProCare
Monitor will result in the formation of
an electromedical system and thus
must comply with the requirements of EN 60601-1-1/ IEC 601-1. All host port
signals are NON-ISOLATED and should be connected to equipment
conforming to IEC-601-1, configured to comply with IEC 601-1-1 ONLY.
Where isolation of data communication is required, GE Medical Systems
Information Technologies part number ILC1926 should be used. If external
alarm control is required, GE Medical Systems Information Technologies
part number 487208 (Isolated Remote Alarm Cable Assembly) should
ALWAYS be used. When a high-priority condition is displayed on the
Monitor, the remote alarm signal becomes active within 0.5 seconds. The
active state of the alarm signal is an open circuit. In the inactive state the
alarm signal is connected to ground. Please refer to the Information Sheet
included with the isolated remote alarm cable for operational details.
Note: When using remote alarm, the ProCare Monitor should be considered
the primary alarm source. The secondary alarm is used for secondary
purposes only.
Pin # Function
1 Common
2 Inverted TTL Transmit Data
3 Inverted TTL Receive Data
4 +5 volts
5 No connection
6 No connection
7 Common
8 Remote Alarm
9 No connection
10 No connection
11 RS232 Transmit Data (TxD)
12 No connection
13 RS232 Receive Data (RxD)
14 No connection
15 No connection

2009381-001
Product Description: 2.5. Compatible Parts
2.5. Compatible Parts
Reorder Codes Product Code ECAT
DINAMAP ProCare Monitor Operations Manual 2009360-001
DINAMAP ProCare Monitor Service Manual 2009381-001
Battery 633178CR
Power Cord 316579
Printer Paper (box of 10) 089100 E9050KP
DINAMAP Rolling Stand 003215 E9050JB
Pole Mounting Option 2009762-001
Wall Mounting Option 2009763-001
Hose Management Option 2009764-001
Bed Rail Option 2009765-001
Nurse Call 487208CR
NIBP OPTIONS:
Airhose 12 ft Adult/Pediatric, Screw Connector 107365 E9050LH
Airhose 24 ft Adult/Pediatric, Screw Connector 107366 E9050LJ
Airhose 12 ft Neonatal, Quick Disconnect 107368 E9050LK
Airhose 12 ft Adult/Pediatric, Quick Disconnect 88847 E9050KN
CUFF ASSORTMENT PACKS:
CLASSIC-CUF® Assortment pack 2692 E2692J

Includes 1 each: Infant, Child, Small Adult, Adult, Large Adult, Thigh Cuff
CLASSIC-CUF® Assortment Pack, Neonate 2693 E2693J

Includes 2 Neo #1, 3 Neo #2, 5 Neo #3, 5 Neo #4, 5 Neo #3
SOFT-CUF® Assortment Pack 2695 E2695J

SOFT-CUF® Assortment, Neonate 2694 E2694J

Includes 2 Neo #1, 3 Neo #2, 5 neo #3, 5 Neo #4, 5 Neo #5
DURA-CUF® Assortment Pack 2699 E2699J

DURA-CUF® Assortment Pack, Adult 2698 E2698J

Includes 1 each: Infant, CHild, Small Adult, Adult, Large Adult, Thigh Cuff

2009381-001
Product Description: 2.5. Compatible Parts
Reorder Codes Product Code ECAT
DURA-CUF® Assortment Pack, Child 2697 E2697J

Includes 2 Infant, 3 Child, and 1 Small Adult Cuff
Additional Blood Pressure Cuffs are available through http://www.gemedicalsystems.com
TEMPERATURE
IVAC* Turbo Temp Oral Temperature Probe, Long Cord 2008774-001
IVAC* Turbo Temp Rectal Temperature Probe, Long Cord 2008775-001
IVAC* Temperature Probe Covers 88015 E9050KK
SpO2
Nellcor**:
Pulse Oximeter Cable DOC-10 2008773-001
DuraSensor Adult Oxygen Sensor DS100A
Masimo***:
Adult Reusable Sensor, 1/Bx (NR125) 2009745-001
Cable (PC08) 2009743-001
* IVAC is a trademark of Alaris Medical Systems
** NELLCOR is a trademark of Mallinckrodt
*** Masimo is a trademark of Masimo Corporation

2009381-001
Product Description: 2.6. Specifications
2.6. Specifications
This product conforms with the essential requirements of the Medical Device Directive.
Accessories without the CE Mark are not guaranteed to meet the Essential requirements of
0 0 8 6 the Medical Device Directive.
The ProCare Monitor is protected against vertically falling drops of water and conforms to
IPX1 the IEC-529 standard at level IPX1. Vertically falling drops shall have no harmful effects to
the monitor.
Power Requirements
MAINS Protection against electrical shock - Class II
AC INPUT VOLTAGE 120 VAC/60 Hz 24W
Alternate Sources Protection against electrical shock - Class II
DC INPUT VOLTAGE 24 VDC (nominal), at 1A
The AC Mains adapter contains a nonresettable and nonreplaceable fuse.
Battery 6 volt, 3.3 amp-hours. Protected by internal auto-resetting fuse and thermal protection.
Minimum Operation Time 2 hrs (5 min cycle with adult cuff at 25° C, SpO2 active at 60 bpm, temp in monitor mode,
printout of current values every 5 minutes) from full charge.
Fuses The Monitor contains four fuses. The fuses are auto-resettable and mounted within the
Monitor. The fuses protect the low voltage DC input, the battery, the remote alarm output
and the +5V output on the host port connector.
Environmental
Operating Temperature +5° C to + 40° C (-41 F to +104 F)
Storage Temperature -20° C to +50° C (-4 F to +122 F)
Operating Atmospheric
700 to 1060 hecto Pascal
Pressure Range
Humidity Range 0% to 95% non-condensing
Radio Frequency Complies with IEC Publication 601-1-2 (April 1993) Medical Electrical Equipment,
Electromagnetic Compatibility Requirements and Tests, and CISPR 11 (Group1, Class A)
for radiated and conducted emissions.
Mechanical
Dimensions Height: 9.8 in (25.0 cm)
Width: 9.8 in (24.8 cm)
Depth: 6.9 in (17.5 cm)
Weight including battery 7.8 lb (3.5 Kg)
Mountings Self Supporting on rubber feet.
Portability Carried by built-in handle

2009381-001
Mechanical
Classification Information Mode of Operation: Continuous degree of Protection

against harmful ingress of water: Drip-Proof IPX1.
NIBP
CUFF PRESSURE RANGE Adult 0 mmHg to 290 mmHg

Neonate 0 mmHg to 145 mmHg
DEFAULT TARGET: Adult 150 ± 15 mmHg

CUFF INFLATION Neonate 110 ± 15 mmHg
TARGET CUFF INFLATION Adult 100 - 250 mmHg (5mmHg Steps)

ADJUSTMENT RANGE Neonate 100 - 140 mmHg (5 mmHg Steps)
BLOOD PRESSURE Adult 120 seconds maximum

DETERMINATION TIME Neonate 85 seconds maximum
PULSE RATE: RANGE Adult 30 - 200 BPM ±3%

Neonate 30 - 220 BPM ±3%
BLOOD PRESSURE: Systolic MAP Diastolic

MEASUREMENT RANGES mmHg mmHg mmHg
Adult 30 - 290 20 - 260 10 - 220

Neonate 30 - 140 20 - 125 10 - 110
NIBP ACCURACY Meets AAMI/ANSI standard SP-10

AAMI/ANSI standard: ±5 mmHg mean error
Intra-arterial method: ± 8 mmHg standard dev.
Temperature - Alaris Thermometry
SCALES Fahrenheit Celsius
RANGE Max 42.2° Celsius 108.0° Fahrenheit

Min 31.6° Celsius 88.9° Fahrenheit
Monitor Mode Accuracy ±0.1° C ± 0.2° F (when tested in a calibrated liquid bath; meets
ASTM E1112, Table 1 in range specified)
Predictive Mode Accuracy ±0.6° C ±1.0° F
Determination Time Less then 60 seconds
SpO2 - Nellcor Pulse Oximetry
SpO2 Range and Accuracy adult/neonate: 70-100% ±3.5 digits
Pulse Rate Range and Accuracy 30 - 250 BPM ±3 BPM
Saturation Pitch Indicator Pitch changes with saturation
The Monitor detects the connection or disconnection or a

Sensor Connect/Disconnect from Patient
sensor to the patient within 15 seconds

2009381-001
SpO2 - Nellcor Pulse Oximetry
The monitor detects the attachment or disconnection of a

Sensor Connect/Disconnect from Monitor
sensor from the Monitor within 5 seconds.
The Monitor detects a pulse of enters a no-signal state

Pulse Detection
within 15 seconds of being attached to a patient.
the monitor detects loss of pulse from patient and enters a

Loss of Pulse
no signal state within 10 seconds.
Nellcor Sensors - SpO2 Range 70% to 100%
OxiMAX Sensor Models Single Patient Use
MAX-A,* MAX-AL* ±2
MAX-N†* ±2
MAX-P* ±2
MAX-I* ±2
MAX-R‡ ±3.5
OxiCliq Sensor Models Single Patient Use
OxiCliq A ±2.5
OxiCliq P ±2.5
OxiCliq N† ±2.5
Reusable Sensor Models
D-YS ±3
D-YS & D-YSE ±3.5
D-YS & DYSPD ±3.5
DS-100A ±3
OXI-A/N ±3
OXI-P/I ±3
* The accuracy specification under motion conditions is ±3. For a definition of motion contact GE Medical Services
Technical Support.
† The MAX-N and the OxiCliq N were tested on patients > 40 kg.
‡ The accuracy specification has been determined between saturations of 80-100%
SpO2 - Masimo Oximetry
Saturation Range 1% - 100%
Pulse Rate and Accuracy 25-240 BPM ±3 digits
Perfusion Range 0.02 to 20%

2009381-001
SpO2 - Masimo Oximetry
Accuracy and Motion Tolerance
Without Motion - Adult/Ped* 70 to 100% ±2 digits
Without Motion - Neonate* 70 to 100% ±3 digits
With Motion - Adult/Ped/Neo**† 70 to 100% ±3 digits
Low Perfusion‡ 70 to 100% ±2 digits

0 to 69% unspecified
Pulse Rate
Without Motion 25 to 240 beats/min ±3 digits
With Motion normal physiologic range

25 to 240 beats/min ±5 digits
* The Masimo SET® SpO2 parameter with LNOP-Adt sensors has been
validated for no motion accuracy in human blood studies on healthy adult
volunteers in induced hypoxia studies in the range of 70-100% SpO2 against
a laboratory co-oximeter and ECG monitor. This variation equals plus or
minus one standard deviation. Plus or minus one standard deviation
encompasses 68% of the population.
**The Masimo SET® SpO2 parameter with LNOP-Adt sensors has been
validated for motion accuracy in human blood studies on healthy adult
volunteers in induced hypoxia studies while performing rubbing and tapping
motions at 2 to 4 Hz at an amplitude of 1 to 2 cm and a nonrepetitive motion
between 1 to 5 Hz at an amplitude of 2 to 3 cm in induced hypoxia studies in
the range of 70-100% SpO2 against a laboratory co-oximeter and ECG
monitor. This variation equals plus or minus one standard deviation. Plus or
minus one standard deviation encompasses 68% of the population.
†The Masimo SET® SpO2 parameter with LNOP-Neo Pt sensors has been
validated for neonatal motion accuracy in human blood studies on neonates
while moving the neonate’s foot at 2 to 4 cm against a laboratory co-
oximeter and ECG monitor. This variation equals plus or minus, one
standard deviation.Plus or minus one standard deviation encompasses 68%
of the population.
‡The Masimo SET® SpO2 parameter with has been validated for low
perfusion accuracy in bench top testing against a Biotek Index 2 stimulator
and Masimo’s simulator with signal strengths of greater than 0.02% and a %
transmission of greater than 5% for saturations ranging from 70 to 100%.
This variation equals plus or minus, one standard deviation.Plus or minus
one standard deviation encompasses 68% of the population.

2009381-001

2009381-001
3 Principles of Operation

2009381-001
For your notes

2009381-001
Principles of Operation: 3.1 Introduction
3.1 Introduction
This section provides overall theory of operation and functional description
of the ProCare Monitor. The ProCare Monitor comes in six different
configurations:
• ProCare 100 - Capable of monitoring Blood Pressure (BP) and Pulse

• ProCare 200 - Capable of monitoring Blood Pressure (BP), Pulse, and
Temperature
• ProCare 300 Nellcor - Capable of monitoring Blood Pressure (BP), Pulse

and SPO2 (Nellcor technology)
• ProCare 300 Masimo - Capable of monitoring Blood Pressure (BP), Pulse

and SPO2 (Masimo technology)
• ProCare 400 Nellcor - Capable of monitoring Blood Pressure (BP), Pulse,

SPO2 (Nellcor technology), and Temperature
• ProCare 400 Masimo - Capable of monitoring Blood Pressure (BP), Pulse,

SPO2 (Masimo technology), and Temperature
The model of your monitor determines which parameters are in your monitor.
Using the ProCare monitor, a clinician can view, print and recall data that is
derived from each parameter. The Monitor is also capable of alerting the
clinician to changes in the patient’s condition. All of the main operations of
the ProCare Monitor are easy-to-use and only a button-touch away. Please
review the factory default settings and, where applicable, enter settings
appropriate for your use.

2009381-001
Principles of Operation: 3.2 Overall Principles of Operation
3.2 Overall Principles of Operation

The following paragraphs provide a general system interface relationship.
The general block diagram is located in Figure 3-1.
The ProCare Monitor is a portable unit that receives input power from an
internal rechargeable battery.
When the ON/OFF button is pressed, the Main Board is brought out of a
sleep mode and turns on the power regulators. The power regulators provide
conditioned power from the Lead Acid Battery. The external DC source is
used only to charge the Lead Acid Battery. Once the ProCare Monitor is
energized, a self-test is performed. The self-test automatically tests the main
functions of the ProCare Monitor. Failure of the self-test will set the ProCare
Monitor into a fail-safe mode with an audio alarm.
Under normal operating condition, the ProCare Monitor is ready to record

the patient vital signs using three external attachments: the temperature
probe, SPO2 sensor, and cuff. Interface with a central station or other device
is accomplished through the host communication port on the back of the
ProCare Monitor.
3.2.1 SpO2 (Model 300 and 400)

The SpO2 probe has a built-in sensor. When the SpO2 sensor is attached to
the SpO2 connector and patient, the probe senses the heart rate and oxygen
saturation. The analog signals are routed to the SpO2 PWA (Nellcor or
Masimo). The analog signals are analyzed on the SpO2 PWA. The results
are digitized and sent to the Main Board via opto couplers. The couplers
provide patient isolation as well as serial data interface. The Main Board
temporarily stores the data and routes it to the UI Board for display and/or
printer.
A reset signal to the SpO2 PWA is also provided so that the power up
sequencing is corrected. If the SpO2 circuit quits communicating to the Main
Board, the Main Board will attempt to reset the SpO2 PWA.
3.2.2 Cuff Blood Pressure (BP) and Pulse

When the cuff and hose are attached to the ProCare Monitor and a Non-
Invasive Blood Pressure (NIBP) determination is initiated, the pump inflates
the cuff. Pressure transducers PT1 and PT2 monitor pressure information.
The pneumatic manifold has one valve, which is used to deflate the cuff.
Valve control is through the Main Board. Once determinations are made for
the systolic BP and diastolic BP, the Main Board calculates the pulse rate/
Mean Arterial Pressure (MAP). The results are then displayed on the UI
Board and sent to the printer (if specified).
The Pneumatic Valve/Manifold (PVM) device is controlled by the secondary

processor. The secondary processor monitors pressure information from
PT2. If an over-inflation condition occurs, the OVERPRESSURE signal is
routed to the PVM to release the air pressure. The Main Board also
generates an alarm condition with the speaker sounding and error code
message on the UI Board.

2008381-001
Principles of Operation: 3.3 Functional Description
3.2.3 Temperature (Model 200 and 400)

The ProCare Monitor uses Alaris Turbo Temp technology to measure patient
temperature. The Turbo Temp probe contains a heating element that pre-
heats the probe to reduce determination time. The heating function is
controlled by the Main Board. The Turbo Temp probe also contains a
thermistor that indicates the temperature. When the probe is attached to the
temperature connector and patient, the signal generated by the thermistor is
routed to the Main Board. The Main Board converts the thermistor signal
along with status information (i.e ORAL or RECTAL probe indicators) to a
DIGITAL signal. The Main Board then processes the DIGITAL signal and
displays the patient temperature on the UI Board and printer in Celsius or
Fahrenheit.
3.2.4 Host Communication Port

The Host Comm Port is used to interface the ProCare Monitor with other
electronic devices (a central nurse's station or remote alarm device.) Signals
can be sent to the ProCare Monitor to initiate blood pressure determinations
and other functions. Patient data can also be retrieved through this port. For
further information, reference the Dinamap ProCare Series Host
Communication manual.
3.3 Functional Description

The following paragraphs provide the functional interface relationship. The
ProCare Monitor contains a number of electrical & electro-mechanical
assemblies. These assemblies are:
* Main Board PWA
* User Interface (UI) Board PWA
* SPO2 PWA (optional)
* Printer (optional)
* Pneumatic Valve/Manifold (PVM)
* Optical Switch (optional)

2009381-001
3.3.1 Main Board PWA

The ProCare Main Board is based on the Motorola MMC2107 integrated
microprocessor. The microprocessor integrates Flash ROM, RAM, A/D
converter with input multiplexor, SPI interface, and timers into one chip. This
microprocessor is the primary processor for the ProCare Monitor. It services
and controls the Patient Parameter Interface (PPI) devices, printer, UI
Board, Real Time Clock, audio circuit, and host communication. The
secondary processor controls the watchdog, pneumatic safety interlock,
timing check, primary processor reset, and power supply control. The
secondary processor is powered at all times.
Independent software in the primary and secondary processor periodically

communicate when the software systems are operating properly. When
either system stops processing or detects an error, it stops communicating
with the other. Either system, upon detecting a failure, can assert a safe
state (herein called FAILSAFE) of the hardware.
Upon entering a FAILSAFE condition, the Main Board will perform the
following tasks:
* Parameter monitoring disabled
* Alarm tone sounding from speaker
* Pneumatic FAILSAFE (deflate the cuff, pump off)
* Normal communications interface disabled
* Remote alarm control inactive
* Hard keys except ON/OFF key inactive
The ON/OFF key can reset the Monitor and end the FAILSAFE condition.
The FAILSAFE condition will terminate automatically after 10 minutes to
preserve battery power.
All regulated DC power, isolated and non-isolated is generated on the Main

Board from Battery supply. The external DC input is used to charge the
battery via charging circuitry on the Main Board.
3.3.2 User Interface (UI) Board PWA

The UI Board is used as a message center. It displays patient vital signs,
alarms status, monitor set-up, limit violation, BP cycle and the time the data
was received. The primary processor on the Main Board controls the UI
Board. When the primary processor reads the parameter signals, it decodes
the signals and routes the display information to the UI Board.
The UI assembly also provides hardkey switches for the ProCare Main
Board. The primary processor asserts a HIGH on the 16 outputs of the 1-of-
16 decoder/demultiplexer one at a time and then reads at the signal on
SW_MUX. A LOW on SW_MUX indicates that the switch is asserted.

2008381-001
3.3.3 SPO2 PWA

The ProCare monitor can be configured for use with either a Nellcor or
Masimo SPO2 PWA. The SPO2 PWA provides continuous readings of
oxygen saturation and pulse rate. Additional circuitry on the Main Board
provides power, data communications, and isolation between SPO2 PWA
and primary processor.
Patient data received from the finger sensor is filtered, amplified, and
analyzed on the SPO2 PWA. The information is sent to the Main Board via
the optically coupled electrically isolated serial connection. The primary
processor receives the data and routes it to the UI board for display. The
data is also sent to the printer if specified.
3.3.4 Printer
The printer receives power from the Main Board and communicates with the
primary processor. Printer presence and print head temperature is indicated
by PR_TH signal to the primary processor. When a print command is sent to
the printer from primary processor, the following will occur:
* PR_CLK signal - transfer the data into print head
* PR_DI signal - serial dot to be printed
* PR_LAT signal - latch the data stream into the head
* PR_ST1-6 - cause the head to print various sections
* PR_M1-4 signals - control power sequentially to the two stepper motor

windings
Together these signal (CONTROL DATA) cause the printer to print a graphic
hardcopy of the patient vital sign values and trend data. It also causes the
printer to print a hardcopy of error logging and service record data.
The printer has a built-in sensor to monitor the printer paper presence. When
the printer is out of paper, it sends a PAPER OUT signal to the primary
processor.
3.3.5 Pneumatic Valve/Manifold (PVM)

The PVM assembly consists of a pump, a deflate valve, and a dump valve.
The PVM inflates/deflates the cuff during BP determinations. During normal
operation the PVM is controlled by the primary processor. If a failsafe mode
or overpressure condition occurs, the secondary processor provides the
appropriate control signals to insure a safe condition, where the cuff vents to
ambient atmosphere pressure.
3.3.6 Optical Switch

The optical switch indicates whether the temperature probe is inserted in the
probe holder or not. The Main Board powers the switch.

2009381-001

2008381-001
Optical Switch
Main Board
SpO2 Probe
SpO2 Circuit
(Optional)
Isolated DC
Power Supply
Tubing
tubing Pump/Valve PT1/ PT2 Pneumatic
BP Cuff Control
Manifold NIBP Data Control
UI Board
Temp Probe Temp Control/ Data
Temp
(Optional) Control Switches
Interface
External DC Regulated Display

6V Battery DC Power LEDs
Control / Data
Real Time
Host Comm RS-232 Clock
Port (rear)
Remote Alarm
Audio
Printer Driver
Control
Control/
Data
Speaker Printer
ProCare Vital Signs Monitor -
System Block Diagram (1 of 2)
page 3-9/10
Real Isolated
Time Power
Clock Supply
External DC
Regulated DC
Power Supply
6Volt Battery
Printer
Drivers
Audio
Speaker
Control
Pneumatic
Valve Control
PT1/PT2
NIBP Data
SpO 2
Interface
Host
Communications
Temp Probe Temperature Temperature

Control
(optional) Control/Data ProCare Vital Signs Monitor -
Main Board Diagram (2 of 2)
page 3-11/12
4 Calibration &
Maintenance

2009381-001
For your notes

2009381-001
Calibration & Maintenance: 4.1 Introduction
4.1 Introduction
This section contains general Monitor service procedures, including alarm
code interpretation, service mode operation, and periodic maintenance and
battery care. Refer to Section 5 for disassembly and reassembly procedures
and related component service information.

2009381-001
Calibration & Maintenance: 4.2 Configuring Your ProCare Monitor
4.2 Configuring Your ProCare Monitor

4.2.1 Unpacking and Preparation for Installation
1.Unpack and identify the contents of all shipping materials.
2.Remove the ProCare monitor.
3.Unpack the external DC Power Input.
4.Insert the external DC Power Input connector into the DC input on the
lower right side of the monitor.
5.Plug the DC Power Input transformer into a Hospital Grounded AC

receptacle. The word CHARGING will illuminate green on the front of the
monitor indicating that an external power source is available.
Prior to usage, it is necessary to charge the monitor for 12 hours.
4.2.2 Set the Date and the Clock

Setting the Date and Time
To set the date and time on the ProCare Monitor, you must first access the
configuration mode. The following table illustrates the menus and the
corresponding LCD display graphics.
Setting Window Text in Window
SpO2 Averaging Pulse Rate and SpO2
SpO2
Temp Unit of Measure Temperature
Year Systolic
Month MAP/Cuff
Day Diastolic
Hour min
Minute min
Procedures
1. With the Monitor off, press and hold the Menu button at the same time as
pressing the On/Off button for 3 seconds.

2009381-001
Calibration & Maintenance: 4.2 Configuring Your ProCare Monitor
2. The Monitor automatically switches on in configuration mode.
3. To set the date and time, press the Menu button to move from one setting
to another. (You will need to press the Menu button several times until the
year setting appears. Use the +/- buttons to increment or decrement the
individual settings.) Once you are finished changing a setting, press the
Menu button again to move to the next setting.
Note: For the date and time to be saved, you must advance the menu
through the min setting.
4. To exit config mode, press the On/Off button.
4.2.3 Parameter Level Functional Testing

After the initial configuration is complete, perform functional testing of each
of the parameters, using the accessories supplied with the ProCare Monitor.
Refer to the ProCare Operator's Manual for more detailed parameter-

specific instructions.
Perform a blood pressure by connecting the supplied hose and cuff together,
then attaching to the front of the ProCare Monitor. Press the Inflate/Stop on
the front to begin the NIBP cycle.
Connect the supplied temperature probe to it’s corresponding connection. A

predictive temperature will begin once the probe is removed from its holster.
Replace the probe after completion of the Temp cycle.
·The SpO2 sensor is an assembly consisting of two parts: the DS-100A, and
the extender cable DOC-10. Connect the cables prior to attaching to the
monitor. An SpO2 reading will be displayed within moments of attaching the
sensor to either a Nellcor simulator or to your finger.

2009381-001
Calibration & Maintenance: 4.3 Periodic Maintenance
4.3 Periodic Maintenance

4.3.1 As Required
Perform the following maintenance procedures as required.
4.3.1.1 Integrity of Hoses and Cuffs
When the pneumatic integrity of any NIBP cuff and hose is in doubt, replace
the cuff and hose, and discard the questionable accessories.
4.3.1.2 Cleaning of Monitor
CAUTION: Do not clean Monitor with isopropyl alcohol or other solvents.
Wipe the exterior of the Monitor with a cloth slightly dampened with mild
detergent or normal hospital bactericides. Use dishwashing detergents such
as IVORY and JOY (registered trademarks of Procter & Gamble Corp.), or
PALMOLIVE (registered trademark of Colgate-Palmolive Corp.)
Do not immerse unit.
4.3.1.3 Cleaning of Accessories
Clean the adult cuffs supplied for use with the monitor by hand washing in
warm, soapy water. However, take care to avoid entry of water into the cuff
and hoses at any time. If water enters the cuff, dry the cuff by passing air
through it.
The neonatal cuffs are for single patient use - discard if they become soiled.
Clean cuffs and hoses with a cloth slightly dampened with mild detergent.
Do not immerse hoses.
Do not immerse cuffs without prior application of cuff hose caps.
Clean SpO2 sensor surface before and after each patient use. Clean SpO2
sensor with a cloth slightly dampened with a mild detergent. Wipe SpO2
sensor to ensure all detergent residue has been removed.
Compatible cleaning and disinfecting solutions are:
Chlorine bleach disinfectant, 5.25%, 0.75 cup per gallon of water.
CAUTION: Do not apply isopropyl alcohol to the Monitor - some parts can
become marred and cracked.

2009381-001
Calibration & Maintenance: 4.3 Periodic Maintenance
Cidex Formula 7 (registered trademark of Johnson & Johnson Medical

Products, Inc.) or pHisoHex (registered trademark of Winthrop-Breon
Laboratories.)
Quaternary-based germicidal detergents like VESTAL INSURANCE

(registered trademark of the Vestal Corp.), HI-TOR PLUS (registered
trademark of the Huntington Corp.), or VIREX (registered trademark of S.C.
Johnson & Son Corp.)
For the above, follow manufacturers' recommendations for dilution rate and
use. These recommendations are not an endorsement of the manufacturers
or of the effectiveness of these materials for cleaning or disinfecting.
4.3.1.4 Long-Term Storage
If it becomes necessary to store the Monitor for an extended period of time,

remove all attached accessories. Attach the original packing inserts, and
place the monitor into the original shipping container.
Long-term storage of a discharged lead-acid battery can permanently

degrade its storage capacity. Therefore, the battery should be fully charged
before storage.
Batteries in storage should be charged every six months to maintain their

capacity.
Elevated temperatures will shorten battery life and can lead to permanent
battery damage.
4.3.2 Annual Procedures

Perform the test procedures described in section 4.6 every twelve months,
or whenever the accuracy of of the monitor is in doubt.

2009381-001
Calibration & Maintenance: 4.4 Care of the Storage Battery
4.4 Care of the Storage Battery

The Monitor uses one Lead-Acid storage battery. The battery can be
charged at any time without reducing the charging capacity.
4.4.1 Battery Charging

The Monitor charges the Lead-Acid battery whenever the AC power supply
is in use. The Monitor automatically senses if the battery needs recharging.
Battery charging will continue as long as the Monitor is connected to the AC
power supply, even when the Monitor is turned off.
·Batteries should be charged before first use or after long periods of storage.
·The battery should be charged for 8 hours before use, as a charged battery
loses some charge when left in storage. It is possible to use the Monitor
while the Monitor is charging.
·The battery should be charged at room temperature (59° F - 86° F; 16° C -

30° C).
·It is normal for the battery to become warm during charging or after use.
·Batteries can be charged or topped-off at any time. It is not necessary to

wait until they are fully discharged.
·If the monitor is idle for extended periods, it should be fully charged once a
month to ensure optimum performance.

2009381-001
Calibration & Maintenance: 4.5 Safety Testing
4.5 Safety Testing

To adequately test the safety and integrity of the ProCare Monitor, the
following test equipment is recommended:
• 12VDC Power Supply
• DMM (Fluke 8842 or equivalent)
• NIBP Analyzer (DNI Nevada "Cufflink" or Equivalent)
• Adult BP Cuff, Neonate BP Cuff, hose, inflation bulb, and mandrel
• Inflation bulb and associated tubing
• Calibration Kit, p/n 320246 available through GE Medical Systems
• SPO2 Simulator (for appropriate SPO2 type if SPO2 is installed)
• SPO2 Cable (for appropriate SPO2 type, if SPO2 is installed)
• TE 1811 Temperature Probe Simulator (if TEMP is installed.) The

Temperature Simulator for the Alaris System is available from Alaris Medical
Systems, Inc. (619) 458-7000
• Printer Paper (if PRINTER is installed)

CAUTION! Calibration equipment should always be kept dry and free of
particulate matter. Moisture or foreign substances introduced to the
pneumatic system will likely cause damage to the monitor and/or the
accessories.
Complete the Test Record (Appendix A) as tests are performed.
Note: This test is written so that a knowledgeable technician who is familiar

with the ProCare monitor and the test equipment and will be able to follow
the test procedure.
Note: To enter service mode press and hold the CYCLE buttons while
pressing the ON/OFF button for 3 seconds.
Notes on Electrical Safety Testing of the ProCare Monitor:
The DINAMAP® ProCare Monitor is designed and tested to meet electrical

safety standard IEC 601-1. Requirements in this standard parallel
requirements in NFPA99 relating to electrical safety. This product meets the
requirements of NFPA99 section 7-5.1.2.2. (grounding of appliances)
through the use of double insulation in the external power supply module
(“Power Brick”.)
The absence of a ground connection on the power brick obviates the need
for any ground resistance test, such as that described in NFPA99 section 7-
5.1.3.2. (Some non-USA Power bricks are equipped with a non-conductive

2009381-001
Calibration & Maintenance: 4.5 Safety Testing
pin at the ground pin location to aid mechanical retention of the Power Brick
into the receptacle.)
Dielectric strength (“Hi-Pot”) testing of the double (reinforced) mains

insulation (4000 V RMS, 60 Hz) may be done by disconnecting the Power
Brick from the Monitor and applying the Hi-Pot tester as follows: Connect
one lead to the two mains power prongs. Connect the other lead to the
conductive sleeve on the DC output connector at the end of the cord.
Hi-Pot testing of the patient connections (1500 VRMS, 60 Hz) may be done
by connecting one lead of the Hi-Pot tester to the outer shell of a spare DC
connector plug inserted into the DC input connector on the Monitor. The
other lead of the tester should be connected to the patient connection being
tested.
WARNING: Don’t electrocute yourself or anyone else when performing Hi-

Pot testing.
NOTE: Hi-Pot testing is done on every unit at the factory and should not be
repeated unnecessarily nor performed more often than required.
4.5.1 Temp Circuit Leakage Test

1. Setup an IEC 601-1 approved leakage tester to apply 240 VAC to an
isolated circuit.
2. Plug temp probe Hi Pot adapter into the temp jack.
3. Record and verify the temp circuit leakage current.
4.5.2 SpO2 Circuit Leakage Test

1. Setup an IEC 601-1 approved leakage tester to apply 240 VAC to an
isolated circuit.
2. Plug an SpO2 cable into the SpO2 connector on the front of the unit.
3. Plug SpO2 probe Hi Pot adapter in to the DB9 jack at the end of the SpO2
cable.
4. Record and verify the SpO2 circuit leakage current.

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Calibration & Maintenance: 4.6 ProCare Patient Monitor Parameter Tests
4.6 ProCare Patient Monitor Parameter Tests

Complete the Test Record (Appendix A) as tests are performed.
Note: This test is written so that a technician who is familiar with the
ProCare monitor and the test equipment will be able to successfully
complete the test procedures. To enter service mode press and hold
the CYCLE button while pressing the ON/OFF button for 3 seconds.
Saving Changes into Flash Memory: Modifications made to the Monitor’s

settings/configuration must be saved prior to placing the Monitor into
service. The Monitor must be in service mode for any changes to be saved.
Events that require you to manually save to the Monitor’s memory include
calibration attempts and enabling/disabling the Monitor’s parameters (refer
to section 4.6.4.) It is not necessary to manually save following a pressure
transducer calibration verification or simple calibration check.
The number of times the flash memory can be saved is limited. The fatal
alarm error 975 may be issued after this process is performed more than 90
times. Following issuance of this fatal alarm, the monitor must be returned to
the GE Medical Systems Information Technologies Service Center to have
the flash memory reset so that future saves can be performed.
4.6.1 SETUP
1. Connect your NIBP Analyzer to the ProCare Monitor.
2. ‘T’ an inflation bulb into the pneumatic setup
3. Consult the following diagram for pneumatic setup guidelines.

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4.6.2 Leakage Testing

Note: To enter service mode press and hold the CYCLE button while
pressing the ON/OFF button
1. Turn the Monitor ON and enter Service Mode.
2. Press CYCLE button and the min display should change to a 1
3. Close the valve on the inflation bulb
4. Set the NIBP Analyzer to "Leak test" function
5. Press the "Pump" button on the NIBP Analyzer
6. After the system inflates to 200mmHg, wait for the "Wait" on the NIBP
analyzer message to be cleared
7. Press the "Start" button on the NIBP Analyzer to begin the leakage test
8. After 60 seconds the NIBP Analyzer will display the leakage rate
9. Record and verify the leakage rate.
10. Turn the ProCare Monitor off
4.6.3 Pressure Transducer Verification

pressing the ON/OFF button
1. Turn the Monitor ON and enter Service Mode.
2. The HISTORY LED should display 0.
3. Set NIBP Analyzer to "Manometer" function and press "Zero Pressure"
4. Press CYCLE button, HISTORY display should change to a 1.
5. Use the inflation bulb to inflate the cuff, hose and pressure indicator setup
to 200mmHg
6. Record and verify the pressure reading on the top LED display
(SYSTOLIC)
7. Record and verify the pressure reading on the bottom LED display
(DIASTOLIC)
8. Use the valve on the bulb to reduce pressure to 150mmHg
(SYSTOLIC)
(DIASTOLIC)

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(SYSTOLIC)
(DIASTOLIC)
(SYSTOLIC)
(DIASTOLIC)
If any of the tests fail, continue to section 4.6.4. Otherwise, continue to

section 4.6.5
4.6.4 Pressure Transducer Calibration

Perform only if Pressure Transducer Verification is out of tolerance as
specified in Appendix A.
pressing the ON/OFF button.
1. Turn the ProCare Monitor ON and enter Service Mode.
2. The min window should display 0.
3. Open valve on bulb to open pressure system to atmosphere
4. Set NIBP Analyzer to "Manometer" function and press "Zero Pressure"
5. Press CYCLE button until the min window shows 1.
6. Close valve on bulb and manually inflate pressure to 200 mmHg (using
the CuffLink manometer as reference).
7. Press MENU button when pressure reads 200 mmHg to save calibration
setting.
8. Two steps are necessary for burning changes into flash:

a. Press the CYCLE button repeatedly until the number 6 is displayed in
the min window.
Note: the number of remaining changes to the flash memory available are
displayed in the MAP/Cuff window. Following each true calibration, the
Monitor decrements by 1 the number of remaining calibrations available. If
the MAP/Cuff window is displaying a figure of less than 10 and the accuracy
of the Monitor is in doubt, contact General Electric Medical Systems
Information Technologies Technical Support at 1-877-274-8456.
b. Press and hold the MENU button until two beeps are heard (one when

2009381-001
the button is pressed and another after the button has been depressed long
enough for the process to complete.)
9. Turn the ProCare Monitor off
4.6.5 Overpressure Verification

pressing the ON/OFF button.
1. Remain in service mode.
2. Use the inflation bulb to inflate pressure until valve opens.
3. Record and verify pressure at which valve opens.
4. Press CYCLE button so that the min window changes to a 2.
5. Use the inflation bulb to inflate pressure until valve opens.
6. Record and verify pressure at which valve opens.
7. Turn unit off.
4.6.6 Button Testing

1. Turn the Monitor on.
2. Record software revision as shown in the systolic and diastolic display.
3. Press START/STOP button.
4. Verify an NIBP determination has been initiated.
5. Block pump port and verify "E80" alarm.
6. Press SILENCE button, verify alarm has been silenced.
7. Verify flashing red indicator of Silence.
8. Press the SILENCE button, verify alarm condition is removed
9. Press ALARM button several times, verify unit cycles through all alarm
settings (i.e SYS, DIA, SPO2).
10. Turn the Monitor off

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4.6.7 LED Tests

1. Power on the ProCare Monitor.
2. During the power-up self-test verify all 7 segment LED display segments
and all discrete LEDs (except CHARGING LEDs) illuminate and are the
correct color.
LED COLOR MATRIX
RED YELLOW GREEN NOT LIT
Systolic Pulse Rate AUTO CYCLE CHARGING
Diastolic LOW HISTORY
°F BATTERY
°C BATTERY ICON
HIGH (all) ALARM VOLUME
LOW (all) PULSE VOLUME
Alarm Bell Icon INFLATE

PRESSURE
SpO2 Strength Meter
3. Repeat power up cycle until all LEDs are checked.
4.6.8 External DC Verification

1. Plug the DC power cable into the monitor.
2. Verify that the CHARGING indicator is illuminated.
4.6.9 NIBP Determination

1. Set NIBP Analyzer to Adult Mode:
SYS/DIA = 120/80
MAP = 90
BPM = 80
2. Press START/STOP button on the Monitor to begin determination
3. Record and verify systolic, diastolic, map and heart rate from the monitor
display
4. Press CYCLE button to initiate a determination in "Auto BP" mode.

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display
6. Press CYCLE button until is displayed on the HISTORY LED to

initiate a determination in STAT mode.
display
8. Press Start/Stop button, end STAT mode.
4.6.10 NIBP Overpressure Verification

1. Restrict airflow through cuff hose port.
2. Press "Inflate/Stop" to begin NIBP determination
3. Verify that is displayed on the SYSTOLIC display and an audible

alarm sounds
4. Remove the air restriction
5. Press "Inflate/Stop" and verify that the pump does not start
6. Press the "Silence" button
7. Press the "Silence" button again
8. Verify the alarm condition is cleared from the SYSTOLIC display
4.6.11 Temperature (Perform if equipped with Temp module)

The Temperature Simulator for the Alaris System is available from Alaris
Medical Systems, Inc. (619) 458-7000.
1. Disconnect the temp probe from the Monitor.
2. Connect the probe simulator to the Monitor.
4. Set the probe simulator to 80.2° F.
5. Record and verify the reading in the TEMP display is 80.2° F ±0.2° F.
6. Set the probe simulator to 102° F.
7. Record and verify the reading in the TEMP display is 102° F ±0.2° F.
8. Set the probe simulator to B.P. and verify reading is 106.0° F ± 0.2° F.
Press broken probe button down and verify the Monitor displays .

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9. Calibration verification is complete. Disconnect the probe simulator and

install the temperature probe. If the Monitor does not pass the calibration
verification, then the Monitor needs repair.
4.6.12 SpO2 (Perform only if equipped with SpO2 module)

Note for Monitors equipped with Nellcor SpO2:
Nellcor is aware that various Nellcor oximetry platforms have some

interesting behaviors when used with various pulse simulators.
On occasion when testing the integrity of the Nellcor oximetry system,

abnormal results may occur when introducing large changes in the pulse
rate and/or pulse amplitude. Extreme changes in rate sent to the Nellcor
sensor by the SpO2 simulator may cause the SpO2 algorithm to completely
miss in finding the pulse rate.
This is an expected result. To workaround this, incrementally step up or

down the settings on your SpO2 simulator and allow for the Monitor to detect
and display the new pulse rate or saturation.
Nellcor recommends use of the SRCmax Portable Tester for use with
ProCare Monitors equipped with the Nellcor SpO2 system.
Masimo recommends BIO-TEK SpO2 simulators.
1. Connect the appropriate SpO2 simulator and cable to the SpO2 connector.
2. Verify the unit displays a:
Pulse value
Saturation value
Signal Strength Bar Graph
3. Disconnect the SpO2 cable
4. Verify the unit generates a alarm and speaker is sounding
5. Press the SILENCE button.
6. Verify the sound has stopped but the error display remains
7. Re-connect the SpO2 sensor
8. Verify the unit displays a:
Pulse Value
Saturation value
Signal Strength bar Graph

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4.6.13 Printer Output Test

1. Load Thermal Paper into the print mechanism
2. Press PRINT button
3. Verify the printer outputs a record and print quality is good
4.6.14 Communication Port Test

1. Connect unit to a PC terminal emulator.
2. Turn unit on.
3. Type " NC0!E", press "Enter"
4. Verify response from unit " NC+!@"
5. Verify that within 40 seconds the pump starts.
6. Type " ND!5", press "Enter"
7. Verify response from unit " ND+!A"
8. Verify the pump stops.

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Calibration & Maintenance: 4.7 Alarm Code Interpretation
4.7 Alarm Code Interpretation

If any other alarms appear that are not listed in the paragraphs that follow,
record the error message and report the failure to Customer Support. Refer
to the Operation Manual for information about patient alarms and general
procedural alarms.
4.7.1 System Failures

When a system failure is encountered, the error code is displayed on the
screen for five seconds and the system enters failsafe mode. The error code
is logged in the history log.
General system error codes are listed below.
Alarm Conditions and Error Codes

When responding to a Monitor alarm, always CHECK THE PATIENT FIRST
and then check the Monitor, cuff, hose and sensors. Press SILENCE to
reset patient alarm conditions.
NIBP
Alarm Definition Possible Cause
E89 NIBP No Determination Unable to make an NIBP determination due to

insufficient signal.
E84 Timeout Determination time > 2 minutes.

Motion Artifact.
E85 Timeout One cuff pressure at > 1 minute.

Motion artifact.
E83 Timeout: Inflation Inflation time is > 40 seconds

Possible air leak is being detected.
E82 Excess Air in Cuff Residual air in cuff above threshold for successful
auto-zero.
E80 Overpressure Overpressure condition detected
SpO2
E20 SpO2 No Sensor SpO2 sensor not connected.

No sensor code detected.
Sensor failure
E21 SpO2 Replace Sensor SpO2 sensor or cable possibly defective.

Cable not connected properly.

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Calibration & Maintenance: 4.7 Alarm Code Interpretation
E23 SpO2 Sensor off finger No SpO2 signal, check or reposition the sensor
E25 SpO2 No Signal No or very low SpO2 signal, reposition sensor
Temperature / Printer / Miscellaneous
E63 Temp Disconnected or Incorrect type of temperature probe: use

Wrong Probe Type TurboTemp-type temperature probe
E61 Temp Probe Broken Bad temperature probe

Temp probe not properly connected
E66 Temp probe Too Hot Bad temperature probe

Verify monitor with known good accessories
E10 Printer No Paper Printer is out of paper

Printer door open
Printer may be defective
E11 Printer Too Hot
E12 Recorder cannot print Main battery voltage is too low to operate
E00 Memory Lost Refer Monitor to Customer Service
900-
Internal Memory Errors Refer Monitor to Customer Service
999

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Calibration & Maintenance: Appendix A - Test Results Form
Appendix A - Test Results Form

Step Description Min Max Actual Pass-Fail-N/A
4.6.2 Leakage
Leakage Result (mmHg) 0 6
4.6.3 Pressure Transducer Verification
Pressure reading at 200mmHg, top display - Systolic 197 203
Pressure reading at 200mmHg, bottom display - Diastolic 197 203
4.6.5 Overpressure Verification
Overpressure threshold, Adult (mmHg) 305 325
Overpressure threshold, Neonate (mmHg) 155 159
4.6.6 Buttons
Software revision in systolic display (top) on off
Software revision in systolic display (bottom)
NIBP alarm initiated
"E80" displayed on SYSTOLIC display
Audible alarm can be silenced
"Silenced" LEDs flash
Overpressure alarm can be cleared
Alarm button is functioning
4.6.7 Display
All 7-Segment LEDs Light Correct Color
All Discrete LEDs Light, Correct Color
4.6.8 4.6.8 External DC Detection
Charging indicator LED illuminated
4.6.9 NIBP Determination
Systolic reading (mmHg) 107 133

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Calibration & Maintenance: Appendix A - Test Results Form
Step Description Min Max Actual Pass-Fail-N/A

4.6.9 NIBP Determination (continued)
Diastolic reading (mmHg) 67 93
MAP reading (mmHg) 85 95
Heart rate reading (bpm) 76 84
4.6.10 NIBP Overpressure
"E80" displayed on SYSTOLIC display
Pump will not start
Overpressure alarm can be cleared
4.6.11 Temperature Test 80.0°F 80.4°F
Temperature reading at 80.2° F 79.9° F 80.5° F
Temperature reading at 102.0° F 101.8° F 102.2° F
Temperature reading at BP verify reads E61 N/A N/A
4.6.12 SpO2
Pulse Value Displayed
Saturation Value Displayed
Signal Strength Bar Graph Displayed
"E23" displayed on SpO2 display
Alarm is silenced, error display remains
Pulse Value
Saturation Value Displayed
Signal Strength Bar Graph Displayed
4.6.13 Printer Test
Printout is generated cleanly
4.6.14 Communication Port Test
"_NC+!@" is displayed on terminal
Pump stops

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Calibration & Maintenance: Appendix B - Connectivity
Appendix B - Connectivity
CHANT
• Provides HL7 output for electronic Patient Medical Records

• Uses ILCs (Isolated Level Convertors) where required along with the
CHANT software to communicate with the HIS System
Compatible Monitors: DINAMAP XL, Compact, MPS (Select and Portable),

PRO 100-400 series, ProCare Series, and PRO 1000.
Nurse Call System
• When the DINAMAP monitor alarms, the Nurse Call System is triggered.
• Uses a Nurse Call Cable to attach to the System. P/N 487208CR.
Compatible Monitors: Compact, PRO 100-400 Series, ProCare Series, and
PRO 1000.
Alarm View
• Wireless transmitter attached to the Monitor.

• Sends alarms and vital signs results to a pager
Compatible Monitors: Compact, MPS (Select and Portable) PRO 100-400
series, ProCare Series, and PRO 1000.
CIC
• Provides Central Alarm Notification & Data Management.

• Compatible with StatView for paging.
Compatible Monitors: PRO 1000 Version 2 and Dash 2000 (both hardwired)
ApexPro
• Provides Central Alarm Notification and data management.

• Transmits data wirelessly.
• Pro 100-400 Series and ProCare (requires P/N IPC-1931)
PatientNet
• Provides central alarm notification and data management.

• Lethal arrhythmia at the Central Station.
• WMTS frequency hopping spread spectrum.
Note: Dash 2000 is incompatible with PatientNet.
ILC-1926
• Interfaces the PRO 100-400 series or ProCare monitor to ANY hardwired

connection.

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• Requires Cables:
-PRO 100-400, ProCare Series, Compact, Plus: cable p/n 683235
-XL monitor series: p/n 682234
ILC-1927
• Interfaces the PRO 1000 monitor to any hardwire connection.

• Installs into the Communications bay at the rear of the monitor.
IPC1928
• Interfaces the PRO 1000 Monitor to the Unity network, hardwire.

• Installs into the Communications bay at the rear of the monitor.
IPC1931
Connects DINAMAP Monitors to the CIC system.
Transfers vital signs results from the Monitor to the CIC
Requirements for use:
- Plug DINAMAP into ApexPro using the DINALINK cable.

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- Apex version 2
- CIC version 3

2009381-001
Calibration & Maintenance: Appendix C - Display Cover: Removal, Installation
Appendix C - Display Cover: Removal, Installation

To remove the plastic display cover:
1. Place the Monitor on a stable surface.
2. Insert a flat-head screwdriver between the top of the display cover and
the body of the monitor.
3. Twist the screwdriver so that the display cover is slightly separated from
the body of the monitor.
4. Using two hands, grasp the top-middle edge of the display cover and pull
away and down.

2009381-001
Calibration & Maintenance: Appendix C - Display Cover: Removal, Installation
5. The fascia and displays are now visible.
Installing the Display Cover:
1. Place the Monitor on a flat, stable surface.
2. Insert the tabs at the base of the display cover into the slots underneath
the bottom row of LEDs.
3. Using two hands, apply firm pressure to the outside edges, while flexing
the upper middle-edge of the display cover away from the monitor. It is
imperative that even pressure is applied as the plastic retention tabs can
break free from the display cover.
4. Apply steady, even pressure to the opposite sides of the display cover
until an audible click is heard.

2009381-001
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
Appendix D: Replacement Parts and Assemblies

ID numbers reference the explode drawings in Section 5.
ID FRU Number Description Content/comments

1 2009910-001 Main PWA Supplied with Arterial ref product s/w
2 2009911-001 Main PWA- Ausc Supplied with Auscultatory version of Monitor
3 2009912-001 UI PWA
4 2009913-001 Nellcor Module Supplied with mounting spacers.

5 2009914-001 Masimo Module Supplied with mounting spacers.
6 2009915-001 Plastics kit 1. Case, front & rear
2. Handle front & rear with h/w
3. Bulkheads 4 types & NIBP insert.
4. Nellcor & Masimo ‘inside’ labels
5. Std. labels, DC input, No temp side label.
6. Battery door & foam.
7. Help card guide and rubber feet.
8. Printer door (and blanking plate when available).
9. Cable tie hardware
2009916-001 Screw kit All internal hardware, screws, washers etc
7 2009918-001 Temperature 1. Housing front & rear.

2. Mounting bracket and plastic guide.
3. Sensor and cable.
4. Mounting hardware
8 2009917-001 Printer 1. Printer
2. Printer chassis and screw.
3. Printer door with roller and label.
9 2009919-001 Printer door Door with label and roller
10 2009920-001 Pneumatics Pump assembly
11 2009921-001 Dump valve Dump valve and adhesive tape to apply.
12 2011645-001 Kit, Keypads Set, left and right keypads
13 2009922-001 Speaker Include mounting bracket
14 2009923-001 Host comms cable With mounting h/w
2008538-001 Power brick UK UK plug 240V input
2008539-001 Power brick EUR Euro plug 230V input
2009460-001 Power brick US US plug 120V input
15 2010429-001 English 400 lbl kit 1. keypad labels set (LH & RH)
2010478-001 English 300 lbl kit 2. Fascia
2010479-001 English 200 lbl kit 3. Display cover
2010480-001 English 100 lbl kit For language variants reference following pages
16 Help card guides All 3 guides and for each language

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2010429-001 Label Kit English 400 printer
P/N (-001) Language Model Is Printer Installed? Method of NIBP Determination

(Auscultatory is labeled on left keypad)
2010429-001 English 400 Printer Installed Traditional
2010481-001 English 400 Printer Installed Auscultatory
2010485-001 English 400 Traditional
2010489-001 English 400 Auscultatory
2010493-001 French 400 Printer Installed Traditional
2010497-001 French 400 Printer Installed Auscultatory
2010501-001 French 400 Traditional

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2010505-001 French 400 Auscultatory
2010509-001 German 400 Printer Installed Traditional
2010513-001 German 400 Printer Installed Auscultatory
2010517-001 German 400 Traditional
2010521-001 German 400 Auscultatory
2010525-001 Spanish 400 Printer Installed
2010529-001 Spanish 400
2010530-001 Spanish 300
2010531-001 Spanish 200

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2010532-001 Spanish 100

2010534-001 Italian 400 Printer Installed
2010538-001 Italian 400
2010539-001 Italian 300
2010540-001 Italian 200
2010541-001 Italian 100
2010542-001 Swedish 400 Printer Installed
2010546-001 Swedish 400
2010547-001 Swedish 300
2010552-001 Swedish 200
2010553-001 Swedish 100
2010554-001 Dutch 400 Printer Installed
2010588-001 Dutch 400
2010559-001 Dutch 300
2010560-001 Dutch 200
2010561-001 Dutch 100
2010578-001 Chinese 400 Printer Installed
2010593-001 Chinese 400

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2010594-001 Chinese 300

2010595-001 Chinese 200
2010596-001 Chinese 100
2010597-001 Japanese 400 Printer Installed
2010601-001 Japanese 400
2010602-001 Japanese 300
2010603-001 Japanese 200
2010604-001 Japanese 100
2010605-001 Danish 400 Printer Installed
2010609-001 Danish 400
2010610-001 Danish 300
2010611-001 Danish 200
2010612-001 Danish 100
2010613-001 Norwegian 400 Printer Installed
2010617-001 Norwegian 400
2010618-001 Norwegian 300
2010619-001 Norwegian 200
2010620-001 Norwegian 100
2010621-001 Korean 400 Printer Installed

2009381-001

2010625-001 Korean 400
2010626-001 Korean 300
2010627-001 Korean 200
2010628-001 Korean 100
2010629-001 Finnish 400 Printer Installed
2010633-001 Finnish 400
2010634-001 Finnish 300
2010635-001 Finnish 200
2010636-001 Finnish 100
2010638-001 Portuguese 400 Printer Installed
2010642-001 Portuguese 400
2010643-001 Portuguese 300
2010644-001 Portuguese 200
2010645-001 Portuguese 100
2010646-001 Russian 400 Printer Installed
2010650-001 Russian 400
2010651-001 Russian 300
2010652-001 Russian 200
2010653-001 Russian 100

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2010656-001 Hungarian 400 Printer Installed
2010660-001 Hungarian 400
2010661-001 Hungarian 300
2010662-001 Hungarian 200
2010663-001 Hungarian 100
2010664-001 Czech 400 Printer Installed
2010668-001 Czech 400
2010669-001 Czech 300
2010670-001 Czech 200
2010671-001 Czech 100
2010672-001 Slovak 400 Printer Installed
2010676-001 Slovak 400
2010677-001 Slovak 300
2010678-001 Slovak 200
2010679-001 Slovak 100
2010680-001 Polish 400 Printer Installed
2010684-001 Polish 400

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2010685-001 Polish 300
2010686-001 Polish 200
2010687-001 Polish 100
2010688-001 Greek 400 Printer Installed
2010692-001 Greek 400
2010693-001 Greek 300
2010694-001 Greek 200
2010695-001 Greek 100

2009381-001
Assembly Drawings & ProCare Schematics: Appendix D: Replacement Parts and Assemblies
5 Assembly Drawings &

ProCare Schematics

2009381-001
or
see Appendix C in Section 4

for Display Cover removal instructions.
or
Exploded Assembly Drawing -

ProCare Monitor (1 of 2)
page 5-1/2
or
PNEUMATIC TUBING ROUTING Exploded Assembly Drawing -

ProCare Monitor (front case)
page 5-3/4
MAIN PROCESSOR
P3V3
P5A
C47 C45
C50 100nF 25V 100nF 25V P3V3 P3V3
C48 C44
25V 100nF
100nF 25V C46 100nF 25V
R1 R117
100nF 25V 100K 100K
13 22 55 91 97
PR_TH R104
VDD1
VDD2
VDD3
VDD4
VDD5
R84 78 49 1K00
I_CHG PQA0 INT0 PUMP_ON
77 50
10K0 PQA1 INT1 DUMP_ON
76 53
V_DC_MON PQA3 INT2 LATCHED_OVP
75 56
PUMP_I PQA4 INT3 DUMP2_ON
74 57
PT1 PQB0 U9 INT4 ADULT-0
73 58
PT2 PQB1 INT5 PNEU_RESET
FPT 72
PQB2 MMC2107 INT6
60
TP34 R116
71 61
V_BAT_MON_PRI PQB3 INT7 TP33 100K
P3V3 80
1K00 79
VRH
VRL 7
R119 1K00 PA0 PR_DI
48 6
D_FROM_COMM RXD1 PA1 PR_CLK
R108 46 5
D_FROM_SPO2 RXD2 PA2 PR_ST1
47 4
D_TO_COMM TXD1 PA3 PR_ST2
45 3
D_TO_SPO2 TXD2 PA4 PR_ST3
2
1K00 PA5
1
PR_ST4
63
SPI_MISO MISO PA6 PR_ST5
R106 62 100
SPI_MOSI R206 MOSI PA7 PR_ST6
65
SPI_CLK SCK
R201 75R0 TP26
66
SS
17
TP39 TP40 TP41 75R0 PB0 PR_VHON
99 16
T_DE DE PB1 PR_M4
92 15
T_CLK TCLK PB2 PR_M2
93 14
T_TDI TDI PB3 PR_M3
94 11
T_TDO TDO PB4 PR_M1
95 10
T_TMS TMS PB5 PR_EOP_EN
98 9
T_TRST TRST PB6 PR_LAT
8
Place near U9 C32 PB7 PR_EOP
1K00
R103 10P
90
CLKOUT SHDN_TO_PRI
RESET_TEST-0 R62 87 27 R114
0R0 XL2 86
EXTAL PC0
26 1K00
C33 8.0MHZ 10M0 R63 XTAL PC1 SW_MUX
25 R113
10P 1K00 83
RESET
PC2 RTC_DATA
24
R90 84
RSTOUT
PC3
23
TP42
RESET_PRI-0 43
PC4 RTC_CLK
20
1K00 ICOC10 PC5 SPO2_RST-0
42 19
P3V3 R120 41
ICOC11 PC6 IPS_ON
18
40
ICOC12 PC7 CS_SEC-0
R115100K 39
ICOC13 R112
ICOC20
100K 38
ICOC21 PD0
35 1K00 FSP_FROM_PRI
ADC_PWM 37
ICOC22 PD1
34
FAST_OVP-0
CS_DISPLAY 36
ICOC23 PD2
33
DUMP_ON_MON
PWM_VOL PD3
32
D_FROM_TEMP
PWM_PITCH 59
VPP PD4
31
D_TO_TEMP
70 30
VDDH PD5 REM_ALARM-0
P5D 82
VDDA PD6
29
TEMP_PROBE_IN
81 28
52
VSSA PD7 DUMP2_ON_MON
VDDF
51
C49 85
VSSF
69 R107
C12 100NF VDDSYN PE5 FSP_TO_PRI
10N0 25V P5D P3V3 P3V3 88
VSSSYN PE6
68
TP30 1K00
64 67
VSTBY PE7
44
TEST
R118
VSS5
VSS1
VSS2
VSS3
VSS4
C53 P3V3SEC R98 P3V3 R190
C1 C52 C15 100NF C3 C16 C54 100K 10K0
C14 10N0 25V 10U0 10N0 100NF 12 21 54 89 96 10K0
10U0 10N0 100NF
25V
P5A 25V R95
1K00
PE7 needs to be high at start-up
C2 C5
10U0 100NF
25V
Schematic - Main Board

SCHEMATIC
PWA, MAIN BOARD, PROCARE
P/N 2008855 Rev B
(1 of 10) page 5-5/6
+3.3V SECONDARY POWER
PBAT
P3V3SEC
P3V3SEC
RESET 1
VIN
C141 3 U22 5
REAL TIME CLOCK

ON/OFFL LP2985 VOUT
100nF 25V U27 4
BYPASS
16 VCC Q14 3 Q14 C106 C105
C115 2 DTC143ZKA 2U2 C13 GND
2 10U0
9 OSCOUT2
Q13
1
Logic
16V 10N0
Q12
100nF 25V Q10 15
R137 10 OSCOUT1 13
Q9 P3V3SEC P3V3
10K0 Q8 14
11 OSCIN Q7 6
R141 Q6 4 C56
12 RESET 5
49K9 8 GND
Q5
7 25V 100nF
Q4
74LV4060 P3V3SEC U21 R2 R3

SECONDARY PROCESSOR C103 XL3 8
PCF8563T 4K99 4K99
R37 12P0 32.768KHZ 1 OSCI
VDD
CLKOUT 7
1K00
2 OSCO SCL 6 RTC_CLK
PT2_SEC
3 INT
VSS
SDA 5 RTC_DATA
R174 P3V3SEC 4
10K2 P3V3SEC
C55
R43 100nF 25V
R176 1K00
20K0
20
1 MCLR VDD
2 RA0/AN0 RB7 28 FAST_CHG

V_BAT_MON_SEC 3 RA1/AN1 RB6 27 LATCHED_OVP
I_CHG 4 RA2/AN2 RB5 26
25
P5A2
5 RA3/AN3/VREF RB4 FAST_OVP-0
6 24
TP1 RA4 RB3
RB2 23 PNEU_OVERRIDE-0
R175 RB1 22 RESET_PRI-0
10K2 RB0/INT0 21 SW_PWR-0
C35
R177 9 OSC1
U3
20K0 22P0 XL1 PIC16LC73B
4.0MHZ
C34 R35 10
OSC2
22P0 0R0 RC0 11
FSP_TO_PRI 12 RC1/CCP2 RC7/RX 18
13
SEC_ALARM RC2/CCP1 RC6/TX 17
RC5/SDO 16
RC4/SDI 15 FSP_FROM_PRI
RC3/SCK 14 PNEU_RESET
RA5/AN4/SS 7 ADULT-0
SPI_MOSI
AGND VSS
SPI_CLK
8 19
CS_SEC-0
SHDN_TO_PRI
PS_ON
SPI_MISO
SCHEMATIC Schematic - Main Board

PWA, MAIN BOARD, PROCARE P/N 2008855 Rev B
(2 of 10) page 5-7/8
P6VMIN
C66
P5A
100nF 25V
1 VIN
LP2980-5V PNEUMATICS
U7 VOUT 5
P5D PBAT
PBAT
Pump Connector
3 ON/OFF
P5D GND C37
C39
J7
2 2U2
3 16V
220U0 D9
PBAT BAS16
1
PUMP 1 C65 TP37 TP38
2
3 P5D
PBACK_IN PBACK_OUT
4 DUMP 100nF 25V
5 P5D P5D XFPM-050
6 DUMP2 3
C28 PT1 VCC
R51 PT1
1 R36
33U0 5V1 VOUT
2
C140 25V D1 GND

1
0R0 2K0
3 R180 C20 C67
33U0 CAP
6
100NF
25V 1K00 680P 25V
3 3
D10 D27
BAS16 BAS16
1 1
Spare Parts
DUMP_ON_MON U14 P5A P5A
R202 3 4
HCT04
100K
R9 C60
Q7 U14 10K0
SI2306DS 5 6
HCT04 100nF 25V
DUMP_ON
3
TLC2272
1
3 8
U14 1
FPT
2 9
HCT04
8 R10 2
4
DUMP2_ON_MON R203 10K0
U14 U13
11 10
100K HCT04
Q24 R6
SI2306DS C17
U14 10N0 10K0 R83
DUMP2_ON
3
13 12
649K
1
HCT04
C64
2
R204 R205 R173 R121
100K 100K 100K 100K 10N0 P5A
Q17 C61
SI2306DS R29
PNEU_OVERRIDE-0 3 4K99 100nF 25V
1 P6VMIN
VCC 14
R28 ADC_PWM
2 2 1
HCT04
5 C58 4K99 U14
Q9 6
C43 GND
7
SI9410DY 7 100nF 25V
470N
PUMP_ON 8 P5A2
4
2
LP2980-5V
1 VIN
3
U6 VOUT 5
3 ON/OFF C36
5
GND 2U2
Q8 6
2 16V
SI9410DY 7
FAST_OVP-0 4
8
R44 C63
2
1K00
3 C59 100nF 25V
R99 R100 R75

100NF XFPM-050
R5 10K0
25V
3
10K0 10K0 0R10 PT2 VCC
R50 PT2
VOUT 2
GND 1 2K0 C57
R181 C21 100NF
CAP 6 25V
PUMP_I 1K00 680P
PT2_SEC

(3 of 10) page 5-9/10
BATTERY CHARGER
DC Input Power
J3 V_IN PBAT
1
2
FS1 L4 D5 MIC4681-ADJ 68U0 D3
3 2 1
2 VIN SW 3 1 2 2 1
C104 2A5 900NH_0A7 BYG22

L1 BYG22
100nF U17
1
D8 C29 C69 1 SHDN FB 4
C40 C70
R96
1
100nF GND D4 100NF
301K SM6T39CA 33U0 5 6 7 8 220U0 25V
2
25V BYS10 25V
2
R25
V_DC_MON 49K9
C90
R87 100nF
100K
BC_5V
PBAT R39
MC78L05 301K
8 1
IN OUT
U2
C68 VR1
R149 GND 100NF
2 3 6 7 50K CW
0R10 25V
VF = 6.9 V
R150 VC = 7.2 V
0R10
R42
10K0
BC_5V
Battery Connector PBAT C71
R13
J2 4A0 10K0 100nF 25V
1
FS4
2
3 8 OPA2340
R72 D12
C98
MBR2030CTL
2
1 1 3
D14
U15
33U0 2
4 4K99 BAS16
25V
1
R11 R81
R138 10K0 200K

5 OPA2340
10K0 U15 7 C116 R148

6
150K
R92 R147 V = 0.191 V @ 75mA 100nF 25V
100K 100K R76 R182
0R10 0R10
R61
249K
C117 Q15
R93 C91 R146 C118 DTC143ZKA
100NF 100NF Logic
49K9 25V 100K 25V 100nF 25V
R64
4K99
V_BAT_MON_SEC
V_BAT_MON_PRI
I_CHG
FAST_CHG
(4 of 10) page 5-11/12
+3.3 V SUPPLY
PBAT
P3V3
MIC4680-3V3 68U0
2 VIN SW 3 1 2
U12 L2
1 SHDN FB 4
C30 C74 GND
C75
100NF C41 100NF
33U0 25V 5 6 7 8
220U0
25V
R101 25V 1
10K0 25V
D6
2
BYG22
PS_ON Q12 Q18

DTC143ZKA
Logic
SI2307DS
2 ANALOG VOLTAGE SUPPLY (+6.5 V)
1
1
68U0 2
3 P6VMIN
L3
MIC3172 D7
5 VIN VSW 7
2 1
U16 BYG22
4 EN
C93 FB 3 R27 C96 C97 C76
C31
33U0
100NF
25V
SGND GND COMP 12K1 220U0 220U0 100NF
25V
1 8 6 2 25V 25V
25V
R65
1K00
R33
C25 2K87
1U0
16V
PROGRAM CONNECTOR
J1
1 PGM_PS_ON-0
2
3
4
+5.0 V SUPPLY
5
P5D
MIC39101-5V
2 VIN VOUT 3
U5
C38 C72 1 EN
FLG 4
C73 C4
2U2 100NF
25V
GND 100NF
25V
10U0
16V 5 6 7 8
RESET_TEST-0

(5 of 10) page 5-13/14
P3V3
C79
P5D
PRINTER INTERFACE
R123 R59 R58 R57 R56 R55 R54 R122 100nF 25V
100K 100K 100K 100K 10K0 100K 100K 100K 20 19
VCC 2OE
PR_DI 2
1A0
U11 1Y0 18
4 16
1A1 1Y1
PR_ST6 6
1A2 1Y2
14
8 12
PR_ST5 1A3 1Y3
17 3
2A0 2Y0
PR_ST4 15
2A1 2Y1
5
13 7
PR_ST3 2A2 2Y2
11 9
2A3 2Y3
PR_ST2
PR_ST1 HCT240
1OE GND
PR_CLK 1 10
P5A P5A
P5A
P5D
Printer Connector
R91 R60
R97 20K0 30K1 J9
PR_EOP 1M00 TLC2272
8 5 1
7 2
P3V3 6 3
4 4
U13 R89 5
Q11 30K1 6
PR_EOP_EN DTA143XKA 7
Logic 8
R73 9
10
100R 11
PBAT 12
13
14
15
R14 Q5 16
10K0 SI2307DS
17
2
R15 1
18
10K0 PBAT_PR 19
20
3
21
C6 22
PR_VHON Q3 23
DTC143ZKA 33U0 P5A 24
Logic 25V
25
26
R26 27
15K0
PR_TH
P5D
R53
2K0
PR_LAT Q4
DTC143ZKA P3V3 C78
Logic
C77
100nF 25V
25V 100nF
2 13 5
VCC VS2 VS1
PR_M1 3 IN1 OUT1 4
LB1831M
PR_M3 7 IN2 OUT2 6
PR_M2 15 IN3 U4 OUT3 14
PR_M4 11 IN4 OUT4 12
17 19
FG5 FG7
18 20
FG6 FG8
FG1 FG2 FG3 FG4
1 8 9 16

(6 of 10) page 5-15/16
AUDIO ALARMS
P5D
R49
P5D 1R00
3 C
C7
R82 1 Q27 10U0
PWM_VOL
10K0 B MMBT3904LT1 16V
U10
E 2
LM386
C26 R24 C10 R41 3 6 J4
1U0 1 C42
100K 4K99 8
10N0
1
16V
2 5 2
4
7 220U0
R74
R111 C11 R71 C87 2R70 C88
10N0 100NF 100NF
10K0 15K0 25V
C8 C86 25V
Speaker Connector
10U0 100NF
25V
16V
D18
PWM_PITCH 1 3
R94
BAS16
49K9
P5D
C89
SEC_ALARM R124
10N0
10K0
R46
P5D
1K00
P5D
R178
1K00 R179
2K0
3
D15 3
D16
1
5V1 5V1 P5D
1 Q28
Q26 P5D DTC143ZKA
DTC143ZKA Logic
C85
Q25
Comms Connector
Logic
D_TO_COMM DTC143ZKA
FS2
0A3
100nF 25V
HOST COMM
Logic
J6
15 12 16 GND 1
VCC FON FOFF

C84 TTL_TX 2
C83 2 C1+ V+ 3 TTL_RX 3
100NF 100nF 25V
25V U8 5V_FUSED 4
4 C1- GND 5
5 C2+ ICL3221 C81 REMOTE_ALARM-0 6
V- 7
C82 100nF 25V
RS-232_TX 7
100NF RS-232_RX 8
25V
6 C2-
11 T1IN T1OUT 13
External DB15
Connector Mapping
9 R1OUT R1IN 8
J6 NAME DB15
1 EN 1 INVALID 0
GND
1 GND 1
D_FROM_COMM P5D 14 2 TTL_TX 2
3 TTL_RX 3
Q13 4 5V_FUSED 4
FS3
0A3
DTA143XKA
Logic 5 GND 7
6 REMOTE_ALARM-0 8
R110
10K0 7 RS-232_TX 11
Q6 8 RS-232_RX 13
NDT3055L
1
D2
REM_ALARM-0 SM6T15CA
2
R102
10K0

(7 of 10) page 5-17/18
Test Connector
P3V3
C92
R22 R19 R18 R17 100NF
25V
10K0 10K0 10K0 10K0
P3V3 P5D PBAT Display Connector

J10
T_TDI 1
2
T_TDO 3 R125
4 10K0
T_CLK 5
6
7
J5
8 1
RESET_TEST-0 9 2
T_TMS 10
SW_MUX 3
11 4
T_DE 12
CS_DISPLAY 5
13
SW_PWR-0 6
T_TRST 14
SPI_MOSI 7
SPI_CLK 8
9
R21 R133 R134 R135 CHARGING_LED 10
1K00 V_IN
499 499 499
R127 R126
100K 100K
ISOLATED POWER SUPPLY

P5TEMP
L12 D19 MIC39101-5V
2 1 2 VIN VOUT 3
C147 MCB1608S102E BYG22 U29
330P C148 C121
C122 100NF 1 EN
FLG 4 10U0
R200 10U0 25V GND
150 5 6 7 8
ISOLATION BARRIER
C126
10U0
R185 C124 C149 N5VSP
PBAT SP
10U0
100NF MIC5270-5.0 SP
4K99 25V
2 GND
D21 U28-VOUT 4
1 2 5 -VIN
BYG22 DO NOT POPULATE
C151 C129
T1 P5VSP
100NF 33U0 C128 6395-TO12
25V 25V 680P 7 D20 MIC39101-5V
2 2 1 2 VIN VOUT 3
BYG22 U30
R153 8 L11 C150 C125
12 75R0 11 C123 1 EN
FLG 4
10U0
100NF
10U0
VIN L13 MCB1608S102E 25V GND
IPS_ON 15 SD-0 SW 11
5 5 6 7 8
6 SYNC R151 MMZ2012R102A 12

FB 3
C127
4 VC ROC 14 13K7
0.1%
SP
1N0 5 RREF RCC 13

PKG_TYPE=0603 R152 LT1425CS
3K01 U31
9 G3 G1 1
16 G4 G2 8 C101 C102
7 SG PG 10 1N0 1N0
3K15V 3K15V
SP
C145 C146
1N0 1N0
3K15V 3K15V
ISOLATION BARRIER
T

(8 of 10) page 5-19/20
SpO2 Module Connector 10 pin SpO2 Patient Connector
Allow 4mm clearance between these signal and all other board signals J8
FL3 NELLCOR MASIMO
1 8
1
LED + IR LED CATHODE
2 7 2
J11 3
RCAL - RETURN
3 6
4
1
4 5 5
2
Z>200/100MHZ 6
3 INNER SHIELD INNER SHIELD
DET + A 7
4 DET ANODE DET CATHODE
GND 8
5 LED - RED LED CATHODE
DIGICAL 9
6 RCAL
DET - C 10
7 FL1 DIGICAL
TO J1 ON NELLCOR MP506 GND
8
3 2 11
N/C 12
9 4 1
LED - 13
10 Z>200/100MHZ ANALOG GND OUTER SHIELD
N/C NC 14
11 DET CATHODE DET ANODE
LED + 15
12
GND FL2 16
13 3 2
14 4 1
Z>200/100MHZ
J16
1
DET + A
2
DET - C
3
P5VSP
INNER SHIELD
4
INNER SHIELD
5
N/C NC
TO J1 ON MASIMO MS-5 6
OUTER SHIELD 2
7
IR LED CATH
8
D35
OUTER SHIELD
9
3
BAV199
RED LED CATH
10
N/C NC
1
P3V3 P5VSP
R183
Q19
SP
DTA143XKA
U23 10K0
4N35
P3V3
SpO2 Module Connector 14 pin
Logic
R144 1 5
AN C
249 B
6
2 4
CTH E
R129 N5VSP P5VSP

10K0
SP
J12
NELLCOR
P5VSP 1
C-LOCK
P5D 2
3
GND
C119 U25 4
GND
RESET
HCPL-2601 5
100nF 25V R142 GND
C 3
6
SPO2_RST-0 8
VCC
AN
2 3K01 7
+12V (N/A)
ANALOG OUT (N/A)
Q16
7
VE 1 8
6 TRANSMIT (MP506 OUT) TO J2 ON NELLCOR MP506
5
VO
CTH
3 MMBT3904LT1 B 9
RECEIVE (MP506 IN)
GND 10
2 E +5 ANALOG
11
CTS (MP506 IN)
12
D_FROM_SPO2 R136 13
GND
+5V DIGITAL
14
499 GND
R184
P5VSP SP 1K00
P3V3
SP SP
J17
Q20 U26 C120 R139 MASIMO
D_TO_SPO2 DTA143XKA HCPL-2601
1K00 1
100nF 25V +5V
Logic 2
R145 2 VCC
8
3
GND
AN 7
VE
249 6
SP 4
GND
3
CTH
VO 5 TO J3 ON MASIMO MS-5
5
GND 6
GND
7
RESET
8
SP 9
RECEIVE (MS-5 IN)
10
TRANSMIT (MS-5 OUT)
ISOLATION BARRIER SP

(9 of 10) page 5-21/22
P5TEMP
P5TEMP
R166
1K00
C137
U36 R186 100nF 25V P5TEMP
TL431 1 10K0 T
C130
17 AVDD DVDD 1
Temp PGM Connector
2 3 6 7 11 DIN 20
D_TO_T_ADC 6
10U0 12
AD0
D_FROM_T_ADC 5
16V AD1 DOUT 21
13 AD2 SCLK 22
SCLK_TO_T_ADC 4
3
14 AD3
DRDY-0 23
DRDY_FROM_T_ADC 2
1
15 AINCOM
T
U34 CS-0 19 DO NOT POPULATE
P5TEMP R172 P5TEMP
9 REF+
ADS1240 T J15
10 REF-
13K7 6 R156
0.1% CLK_TADC R167 DSYNC-0
3 18
P5TEMP X_IN POL 10K0
Temperature
4 24
100R X_OUT BUFEN
R155
R193 PDWN-0 7
Probe Connector 10K0 3

D24
5 RESET-0
DGND1 2
10K0
ISOLATION BARRIER
BAS16 16 AGND DGND2 8
1
L14 R157
J14 V_THERM
1 BLM11B221SB 1K00 T T
2 L9 C152 C136
3 100NF 100NF
3
D23 25V 25V
4
BLM11B221SB 1
BAS16 P5TEMP P3V3
5
6
T T C138
R154
T
100nF 25V
T P5TEMP U33
4N35 10K0
C133 T
P5TEMP 1
AN C
5
D_FROM_TEMP
P5TEMP 100nF 25V R168 2
B
6
4
CTH E
T
2K0
Q21 R171 R191
3
D28 R194 R195 R196 R197 R164 SI2307DS
15 14 2K21 Q23
30R 30R 30R 30R 499K 2 1K00 VDD1 RB7
DTA143XKA D_TO_TEMP
BAS16 R192 16 13
L7 1 1 VDD2 RB6
4 12 Logic
MCLR-0 RB5
10K0 11
BLM11B221SB
3
19
RB4/PGM
10 T U32 R169
RA0/AN0 RB3
20
RB2/TX
9
4N35
1K00
3 RA1/AN1
D29 1
RA2/AN2/VREF RB1/RX
8 R198 R188 5
C AN
1
BAS16 2
RA3/AN3/CMP1 RB0/INT
7 10K0 100K 6
1
R160 MON_HTR 3 4
B
2
RA4/T0CKI/CMP2 E CTH
10K0
C134
18
OSC1
U35
R187
T T T
100NF PIC16F628
25V 17 10K0
OSC2/OUT
P5TEMP
VSS1 VSS2
T C132 5 6
T
3
D22 22P0 R162
BAS16
XL4
1 4.0MHZ 0R0 T T
L10 C131
BLM11B221SB 22P0
3
D25 TEMP_PROBE_IN
1
BAS16 Q22 T
SI2306DS
3
P3V3
Temp Probe Switch Connector
R158 R189 R132 P5D
10K0
T
EN_HTR 10K0 J13
499K
V_JUMPER C142 1
2
2U2
C135 16V
3
100NF R165
25V
499K T
Schematic - Main Board

T
SCHEMATIC
(10 of 10) page 5-23/24
P5D
C3
PBAT
P5D 100NF
C2
24 PDG_L[0:12]
100NF VCC 11 PDG_L0
Y0
20 9 PDG_L1
Y1
VCC 7 DIG_MUX0 2 10 PDG_L2
IO0 A0 Y2
R127 11 13 DIG_MUX1 3 8 PDG_L3 R1 R13 R4 R3 R5 R6 R7 R8 R9 R10 R11 R12
DS0 IO1 A1 Y3
100R 12 6 DIG_MUX2 21 7 PDG_L4 10K0 10K0 10K0 10K0 10K0 10K0 10K0 10K0 10K0 10K0 10K0 10K0
CLK IO2 A2 Y4 1% 1% 1% 1% 1% 1% 1% 1% 1% 1% 1% 1%
8 14 DIG_MUX3 22 6 PDG_L5
Q0 IO3 A3 Y5 Q15 Q16 Q17 Q18 Q19 Q20 Q21 Q22 Q23 Q24 Q25 Q26
2 HCT299 5 5 PDG_L6
OE1 U5 IO4 Y6 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188 2SB1188
P5D 3 15 4 PDG_L7
OE2 IO5 P5D Y7
1 4 18 PDG_L8 R41 R53 R52 R43 R45 R44 R49 R48 R47 R46 R51 R50
DG11
DG10
DG0
DG1
DG2
DG3
DG4
DG5
DG6
DG7
DG8
DG9
S0 IO6 Y8
19
19 16 17 PDG_L9
180R 180R 180R 180R 180R 180R 180R 180R 180R 180R 180R 180R
PDG_L11
PDG_L10
S1 IO7 Y9
PDG_L0
PDG_L1
PDG_L2
PDG_L3
PDG_L4
PDG_L5
PDG_L6
PDG_L7
PDG_L8
PDG_L9
17 R60 20 PDG_L10
Q7 10K0 HEF4514 Y10
P5D 18 1% U2 19 PDG_L11
CLR GND DS7 Y11 L Q1 L Q3 L Q4 L Q5 L Q6 L Q7 L Q8 L Q9 L Q10 L Q11 L Q12 L Q14
9 1 14 PDG_L12 DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA DTC143ZKA
EL Y12
9 10
23 13
E Y13
16
Y14
R61 15
Y15
P5D P5D 10K0 GND
D1 HCT132 1% DG[0:12]
12
GND R2
U1 10K0
1%
MAP PULSE
BAT54C
R39
Q2
2SB1188 SYSTOLIC
200R LED13 LED10 LED16
DMR20A-1 RED DMR20A-1 RED DMR20A-1 RED LED29 LED28
R42 DG12
180R SA0 2 SA0 2 SA0 2 LTC2621JD RED LTC4624Y YELLOW
C1 A A A
PDG_L12
SA1 15 SA1 15 SA1 15 S8 R104 15 S0 R111 12
R40 100NF B a B a B a A/L1 A/L1
470K SA2 13 SA2 13 SA2 13 S9 R98 620 12 S1 R105 200 11
C C C B/L2 a a a B/L2 a a a
50V L Q13 SA3 11
f b
SA3 11
f b
SA3 11
f b
S10 620 R103 6 L3 S2 200 R110 3 L3
D1 D1 D1 C/L3 C/L3
DTC143ZKA 9 g 9 g 9 g S11 R99 620 1
f b f b f b
S3 R106 200 4
f b f b f b
D2 D2 D2 D L1 D L1
5 5 5 S12 620 R102 4 g g g S4 200 R109 2 g g g
E1 e c E1 e c E1 e c E E
SA4 7 SA4 7 SA4 7 S13 R100 620 16 S5 R107 200 15
E2 E2 E2 F e c e c e c F e c e c e c
P5D P5D d d d 620 R101 200 R108
CONN_S_2X5_HDRF SA5 3 SA5 3 SA5 3 S14 7 L2 S6 8 L2
PBAT C9 F F F G G
HCT132 DP DP DP
d d d d d d
SA6 14 SA6 14 SA6 14 620 3 200 6
V_IN G G G DP DP
DP DP DP DG6 1 DP DP DP
10 100NF 10 10 10 DG0 2 DG1
PBAT DP DP DP DIG1 DG7 5 DG2
9 GND 4 4 4 DG1 5
SPI_CLK P5D U1 COM COM COM DIG2 DG8 7
12 12 12 DG2 138 DIG3
8 HCT132
HCT132P5D
SPI_MOSI COM COM COM DIG3 14
R55 L1,L2,L3 L1,L2,L3
7 17 17 17
SW_PWR COM COM COM
6 R131 100R S0 R14 SA0
DG0
DG1
DG2
CS_DISPLAY GND
5 100R U1 GND S1 R23 330 SA1
P5D P5D U1
4 S2 330 R24 SA2
SW_MUX SA[0:6]
3 S3 R25 330 SA3
GND
2 S4 330 R26 SA4 LED9 GURX10D
RED
1 S5 R27 330 SA5 DIASTOLIC SPO2
LED17 LED18 LED19 1 20
J1 S6 330 R28 SA6
DMR20A-1 RED DMR20A-1 RED DMR20A-1 RED LED27
330 LTC4624JD RED 2 19
SA0 2 SA0 2 SA0 2
A A A S0 R97 12
SA1 15
B a SA1 15
B a SA1 15
B a
A/L1 3 18
S1 R37 330 11
P5D SA2 13 SA2 13 SA2 13 B/L2 a a a
C
f b
C
f b
C
f b S2 330 R96 3
C/L3
L3 4 17
needs pull up on main board SA3 11 SA3 11 SA3 11 f b f b f b
C4 D1 D1 D1 S3 R57 330 4
9
D2
g 9
D2
g 9
D2
g D L1 5 16 R119 S15
S4 330 R95 2 g g g
100NF 5 5 5 E 200
E1 e c E1 e c E1 e c S5 R58 330 15
F
6 15 R120 S14
SA4 7 SA4 7 SA4 7 e c e c e c
E2 E2 E2 S6 330 R94 8 L2 200
R56 SA5 3
F
d SA5 3
F
d SA5 3
F
d G
d d d
7 14 R121 S13
20 DP DP DP 330 1 6
100R DP 200
SA6 14 SA6 14 SA6 14 DG9 DP DP DP
P5D VCC
IO0
7 PS0 G G G 5 DG1 8 13 R122 S12
10 10 10 DG10 DG2
11 13 PS1 DP DP DP 7 200
DS0 IO1 4
COM
4
COM
4
COM
DG11
DIG3
9 12 R123 S11
12 6 PS2 14
CLK IO2 12 12 12 200
8
Q0 IO3
14 PS3 COM COM COM L1,L2,L3 10 11 R124 S15
HCT299 17 17 17
2 5 PS4 COM COM COM 200 S[0:15]
OE1 U4 IO4
DG11
DG3
DG4
DG5
DG6
3 15 PS5
OE2 IO5
1 4 PS6
19 S0 IO6
19 16 PS7
S1 IO7 AUTO/TIME
Q7
17
TEMP LED11
CLR 18 LED30
GND DS7 LTC2623JD RED
P5D 9 LTC4627JD RED
9 10 S8 R118 13
S8 R36 14 A/L1
A S9 R112 620 15
S9 R29 330 16 B/L2 a a a a
B a a a a S10 620 R117 2 L3
S10 330 R35 13 C/L3
C R113 620 f b f b f b f b
f b f b f b f b S11 6 L1
S11 R30 330 3 D
P5D D S12 620 R116 5 g g g g
C5 S12 330 R34 5 g g g g E
E S13 R114 620 16
S13 R31 330 11 F e c e c e c e c
100NF F e c e c e c e c S14 620 R115 7 L2
S14 330 R33 15 G
20 G 620 3 d d d d
S15 R32 330 7 d d d d DP DP DP DP DP
VCC 7 PS8 DP DP DP DP DP DG3 1
P5D IO0 330 DG7 1 DIG1
11 13 PS9 DIG1 DG4 14
DS0 IO1 DG8 2 DIG2
12 6 PS10 DIG2 DG5 11
CLK IO2 DG9 6 DIG3
8 14 PS11 DIG3 DG6 8
Q0 IO3 DG10 8 DIG4
2 HCT299 5 PS12 DIG4 DG11 12
OE1 U3 IO4 L1,L2,L3
3 15 PS13
OE2 IO5
1 4 PS14
19 S0 IO6
19 16 PS15
S1 IO7
17
Q7
CLR 18
GND DS7
P5D 9
9 10
PS[0:15]
DTC143ZKA is a digital transistor with a 4K7 base resistor and a 47K base pull-down resistor
DTD123EK is a digital transistor with a 2K2 base resistor and a 2K2 base pull-down resistor S[0:15]
S10
S9
S11
S12
S13
S14
S15
S1
S2
S3
S4
S5
S6
S7
S8
S0
Schematic -
L Q27
DTD123EK
L Q28
DTD123EK
L Q29
DTD123EK
L Q30
DTD123EK
L Q31
DTD123EK
L Q32
DTD123EK
L Q33
DTD123EK
L Q34
DTD123EK
L Q35
DTD123EK
L Q36
DTD123EK
L Q37
DTD123EK
SCHEMATIC L Q38
DTD123EK
L Q39
DTD123EK
L Q40
DTD123EK
L Q41
DTD123EK
L Q42
DTD123EK
User Interface Board
P/N 2008741 Rev B
PS10
PS11
PS12
PS13
PS14
PS15
PS0
PS1
PS2
PS3
PS4
PS5
PS6
PS7
PS8
PS9
(1 of 2) page 5-25/26
PROCARE USER INTERFACE BOARD
PCB BOARD SWITCH LOCATIONS
SILENCE 2 5 INFLATE
PBAT P5D
ALARM 1 3 CYCLE
C12 C11 C10 C8 C6 C7

+ 7 0 HISTORY
100NF
50V
100NF
50V
100NF
50V
47U0
16V
47U0
16V
47U0
16V
- 6 8 PRINT
MENU 4 9 ON/OFF
V_IN
DG[0:12]
DG3
LED37 DG4
PDG_L[0:11] APTD3216QYC
GREEN
CHARGING DG5
R126
10K0 R135
1% 10K0
LED21 1% R136
APTD3216QYC 10K0
GREEN 1%
LED56
APTD3216SYCK LED54 LED15 LED1
SW9 YELLOW AP3216SURC APTD3216QYC APTD3216QYC
SW_PWR A B BATT BATT RED 2 GREEN GREEN
LED66 LOW LOW BELL BATTERY BATTERY
LEFT RIGHT BATTERY MIDDLE LEFT
ON/OFF APTD3216QYC RIGHT
GREEN LED62 LED61
AP3216SURC AP3216SURC LED69 LED60 LED55 LED68 LED57 LED5
CHARGING RED RED APTD3216SYCK AP3216SURC 1 APTD3216QYC APTD3216QYC
APTD3216SYCK APTD3216QYC
degF degC YELLOW YELLOW RED GREEN GREEN GREEN
LED65
APTD3216QYC
GREEN R20 R18 R75
SW_MUX 38R3 38R3 R133 R77 R134 R16 R74
38R3 22R 38R3
22R 22R 22R
Q43 L SW0 S7 S15 S7 S7 S15 S15 S15 S7

DTD123EK D2 PDG_L0
A B
HISTORY
SW1
BAT54C
A B
PDG_L1
ALARM DG12
SW2
A B LED53 LED40 LED52 LED50 LED49 LED46 LED44 LED42
D6 SILENCE PDG_L2 LED67 AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC
AP3216SURC RED RED RED RED RED RED RED RED
RED PULSE PULSE SpO2 SpO2 DIA DIA SYS
LOW HIGH LOW HIGH LOW HIGH LOW SYS
minus HIGH
R125
10K0 LED38 LED39 LED41 LED51 LED48 LED47 LED45 LED43
BAT54C SW3 1% AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC AP3216SURC
RED RED RED RED RED RED RED RED
A B PDG_L3 R64
CYCLE 38R3
SW4 R79 R65 R63 R38 R21 R19 R17 R15

A B 22R 22R 22R 22R 22R 22R 22R 22R
D5 MENU PDG_L4 S8 S7 S6 S5 S4 S3 S2 S1 S0
SW5
BAT54C A B
INFLATE PDG_L5
DG0
DG1
SW6
DG2
A B
D4 PDG_L6 DG12
MINUS
LED3 LED2 LED58 LED35 LED34 LED32

APTD3216QYC APTD3216QYC APTD3216QYC LED64 LED7 LED22 APTD3216QYC APTD3216QYC APTD3216QYC LED26 LED25 LED24
BAT54C AL VOL GREEN AL VOL GREEN AL VOL GREEN APTD3216QYC APTD3216QYC APTD3216QYC GREEN GREEN GREEN APTD3216QYC APTD3216QYC APTD3216QYC
SW7 GREEN GREEN GREEN GREEN GREEN GREEN
RIGHT MIDDLE LEFT PUL VOL PUL VOL
A B PDG_L7 LEFT MIDDLE PUL VOL AUTO AUTO 2
RIGHT RIGHT LEFT INF PRES INF PRES INF PRES
PLUS HISTORY RIGHT MIDDLE LEFT
LED8 LED6 LED59 LED36 LED70 LED14 LED33
APTD3216QYC APTD3216QYC APTD3216QYC LED63 LED20 LED4 APTD3216QYC APTD3216QYC APTD3216QYC LED31 LED12
SW8 GREEN GREEN GREEN APTD3216QYC APTD3216QYC APTD3216QYC GREEN
APTD3216QYC
GREEN GREEN APTD3216QYC 1 APTD3216QYC
LED23
GREEN GREEN GREEN GREEN GREEN GREEN APTD3216QYC
A B GREEN
D3 PDG_L8
PRINT
R90 R137 R89 R87 R85 R84
R70 R72 R22 22R 38R3 22R 22R 22R 22R R82
22R 22R 22R R62 R68 R80 22R
22R 22R 22R
BAT54C
S7 S15 S15 S7 S7 S15 S15 S14 S14 S13 S12 S11 S10
Schematic -
User Interface Board
P/N 2008741 Rev B
(2 of 2) page 5-27/28
PROCARE USER INTERFACE BOARD
0086
2009381-001 A
gemedical.com
World Headquarters European Representative Asia Headquarters

GE Medical Systems GE Medical Systems GE Medical Systems
Information Technologies, Inc. Information Technologies GmbH Information Technologies Asia; GE (China) Co., Ltd.
8200 West Tower Avenue Munzinger Straße 3-5 24th Floor, Shanghai MAXDO Center,
Milwaukee, WI 53223 USA D-79111 Freiburg 8 Xing Yi Road, Hong Qiao Development Zone
Tel: + 1 414 355 5000 Germany Shanghai 200336, P.R. China
1 800 558 5120 (US only) Tel: + 49 761 45 43 - 0 Tel: + 86 21 5257 4650
Fax: + 1 414 355 3790 Fax: + 49 761 45 43 - 233 Fax: + 86 21 5208 2008

Manu Usu Oper Manto Monit Procare 300 Dinamap

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Manu Usu Oper Manto Monit Procare 300 Dinamap

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DINAMAP® ProCare Monitor

• ProCare 100: BP, Pulse

Reissues and Updates

Errors and Omissions

Part No. 2009381-001 A

Illustrations may show design models; production units may incorporate

Hierarchy of Warnings and Cautions

A general caution is a statement that alerts the user to the possibility of a

© GE Medical Systems Information Technologies 2002, TAMPA, FL 33614

Printed in the U.S.A. All rights reserved.

Revision A ProCare Patient Monitor Service Manual

ProCare Patient Monitor Service Manual Revision A

© GE Medical Systems Information Technologies, 2002. All rights reserved.

T-2 ProCare Monitor Revision A

1.2 Manual Changes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

1.3 Service Policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

1.4 Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

2.2. Product Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3

2.3. Controls, Indicators, and Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

2.4. Host Communications Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

2.5. Compatible Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

3.2 Overall Principles of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

Revsion A ProCare Patient Monitor Service Manual

3.2.2 Cuff Blood Pressure (BP) and Pulse . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

3.3 Functional Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

4 Calibration & Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . 1

4.2 Configuring Your ProCare Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

4.3 Periodic Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

4.4 Care of the Storage Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

4.5 Safety Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

4.6 ProCare Patient Monitor Parameter Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

ProCare Patient Monitor Service Manual Revision A

4.6.11 Temperature (Perform if equipped with Temp module) . . . . . . . . . . . 16

4.7 Alarm Code Interpretation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

Appendix A - Test Results Form . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

Appendix C - Display Cover: Removal, Installation . . . . . . . . . . . . . . . . . . . . . . . . . 25

Appendix D: Replacement Parts and Assemblies . . . . . . . . . . . . . . . . . . . . . . . . . . 27

5 Assembly Drawings & ProCare Schematics

Revsion A ProCare Patient Monitor Service Manual

ProCare Patient Monitor Service Manual Revision A

Revision A ProCare Patient Monitor Service Manual 1-1

To reduce the risk of electric shock, do not

Only qualified technicians should perform repairs to this equipment.

For information about operating the Monitor in a clinical environment, refer to

This Service Manual consists of the following five sections:

Section 2 provides a general overview of the ProCare Monitor including the

Section 3 presents principles of operation for the Monitor, including an

Section 4 provides information about periodic and corrective maintenance of

Section 5 provides component information about the Monitor, including

1-3 ProCare Patient Monitor Service Manual Revision A

1.2 Manual Changes

General Electric Medical Systems Information Technologies

Changes to the Service Manual, either in response to user input or to reflect

Changes occurring between reissues are addressed through Change

1-4 ProCare Patient Monitor Service Manual Revision A

1.3 Service Policy

1.3.1 Service Contracts

Prior to calling, please be prepared to provide:

 product name and model number

 the product serial number

1.3.3 Return to Factory Repair Service

The Customer Support representative will record all necessary information

Revsion A ProCare Patient Monitor Service Manual 1-5

product name and model number

the product serial number

Facility's complete name, address, and phone number

The ability to uses industry standard accessories