Download GE Dinamap ProCare Service manual

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 B
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, 2004 TAMPA, FL.
All rights reserved.
Revision B
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
2009381-001
Revision B
DINAMAP®
ProCare Monitor
Service Manual
2009381-001
Revision B
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, 2004. All rights reserved.
T-2
ProCare Monitor
2009381-001
Revision B
Table of Contents
1
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. . . . . 1-1
1.1 Scope of Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
1.2 Manual Changes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
1.3 Service Policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
1.3.1 Service Contracts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
1.3.2 Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
1.3.3 Return to Factory Repair Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1- 5
1.3.4 Service Loaners . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
1.3.5 Repair Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
1.3.6 Replacement Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7
1.4 Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
1.4.1 General Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1- 8
2
Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
2.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
2.2. Product Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
2.3. Controls, Indicators, and Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4
2.3.1. ProCare Monitor Rear Panel Connections . . . . . . . . . . . . . . . . . . . . . . . 2-4
2.3.2. Front Panel Controls and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
2.4. Host Communications Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
2.4.1. DB15 Connector Pin Assignments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
2.5. Compatible Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
2.6. Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
3
Principles of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
3.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
3.2 Overall Principles of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
3.2.1 SpO2 (Model 300 and 400) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
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3.2.2 Cuff Blood Pressure (BP) and Pulse . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
3.2.3 Temperature (Model 200 and 400) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
3.2.4 Host Communication Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
3.3 Functional Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
3.3.1 Main Board PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
3.3.2 User Interface (UI) Board PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
3.3.3 SPO2 PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
3.3.4 Printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
3.3.5 Pneumatic Valve/Manifold (PVM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
3.3.6 Optical Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
4
Calibration & Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
4.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4- 3
4.2 Configuring Your ProCare Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
4.2.1 Unpacking and Preparation for Installation . . . . . . . . . . . . . . . . . . . . . . . 4-4
4.2.2 Set the Date and the Clock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
4.2.3 Parameter Level Functional Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
4.3 Periodic Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
4.3.1 As Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
4.3.2 Annual Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
4.4 Care of the Storage Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
4.4.1 Battery Charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
4.5 Safety Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Notes on Electrical Safety Testing of the ProCare Monitor: . . . . . . . 4-9
4.5.1 Temp Circuit Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
4.5.2 SpO2 Circuit Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
4.6 ProCare Patient Monitor Parameter Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
4.6.1 SETUP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
4.6.2 Leakage Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
4.6.3 Pressure Transducer Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
4.6.4 Pressure Transducer Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-13
4.6.5 Overpressure Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14
4.6.6 Button Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14
4.6.7 LED Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-15
4.6.8 External DC Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-15
4.6.9 NIBP Determination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-15
4.6.10 NIBP Overpressure Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-16
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Table of Contents
4.6.11 Temperature (Perform if equipped with Temp module) . . . . . . . . . . .
4.6.12 SpO2 (Perform only if equipped with SpO2 module) . . . . . . . . . . . . .
4.6.13 Printer Output Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.6.14 Communication Port Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4-16
4-17
4-18
4-18
4.7 Alarm Code Interpretation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-19
4.7.1 System Failures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-19
Appendix A - Test Results Form . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4- 21
Appendix B - Connectivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4- 23
Appendix C - Display Cover: Removal, Installation . . . . . . . . . . . . . . . . . . . . . . . . . 4-25
Appendix D: Replacement Parts and Assemblies . . . . .. . . . . . . . . . . . . . . . . . . . . . 4-27
Appendix E: Electromagnetic Compatibility . .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-37
5
Revsion B
Assembly Drawings & ProCare Schematics. . . . . . . . . . . . . . . . . . 5-1
ProCare Patient Monitor Service Manual
2009381-001
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ProCare Patient Monitor Service Manual
2009381-001
Revision B
1
Revision B
Introduction
ProCare Patient Monitor Service Manual
2009381-001
1-1
1-2
ProCare Patient Monitor Service Manual
2009381-001
Revision B
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.
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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.
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Revision B
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.
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Introduction: 1.3 Service Policy
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 nonwarranty 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.
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Introduction: 1.3 Service Policy
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 1-800-5585102. Please have the Product Code of the item you wish to order, your
purchase order and account number available.
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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 DCoperated 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.
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ProCare Patient Monitor Service Manual
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2
Revsion B
Product Description
ProCare Partient Monitor Service Manual
2009381-001
2-1
For your notes
2-2
ProCare Partient Monitor Service Manual
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Revision B
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 B
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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 RS232 serial port) for use only with equipment conforming to IEC 601-1,
configured to comply with IEC 601-1.
3 Printer Door (optional.)
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Product Description: 2.3. Controls, Indicators, and Connectors
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.
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Product Description: 2.3. Controls, Indicators, and Connectors
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.
2-6
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Revision B
Product Description: 2.3. Controls, Indicators, and Connectors
Right-Side Panel
30 External power socket: To be used with approved GE Medical Systems
Information Technologies AC-DC power converter ONLY.
Revision B
ProCare Partient Monitor Service Manual
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2-7
Product Description: 2.3. Controls, Indicators, and Connectors
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.
2-8
ProCare Partient Monitor Service Manual
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Revision B
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 #
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
Revision B
Function
Common
Inverted TTL Transmit Data
Inverted TTL Receive Data
+5 volts
No connection
No connection
Common
Remote Alarm
No connection
No connection
RS232 Transmit Data (TxD)
No connection
RS232 Receive Data (RxD)
No connection
No connection
ProCare Partient Monitor Service Manual
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2-9
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
CLASSIC-CUF® Assortment pack
Includes 1 each: Infant, Child, Small Adult, Adult, Large Adult, Thigh Cuff
2692
E2692J
CLASSIC-CUF® Assortment Pack, Neonate
Includes 2 Neo #1, 3 Neo #2, 5 Neo #3, 5 Neo #4, 5 Neo #3
2693
E2693J
SOFT-CUF® Assortment Pack
Includes 1 each: Infant, Child, Small Adult, Adult, Large Adult, Thigh Cuff
2695
E2695J
SOFT-CUF® Assortment, Neonate
Includes 2 Neo #1, 3 Neo #2, 5 neo #3, 5 Neo #4, 5 Neo #5
2694
E2694J
DURA-CUF® Assortment Pack
Includes 1 each: Infant, Child, Small Adult, Adult, Large Adult, Thigh Cuff
2699
E2699J
DURA-CUF® Assortment Pack, Adult
Includes 1 each: Infant, CHild, Small Adult, Adult, Large Adult, Thigh Cuff
2698
E2698J
CUFF ASSORTMENT PACKS:
2-10
ProCare Partient Monitor Service Manual
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Revision B
Product Description: 2.5. Compatible Parts
Reorder Codes
Product Code
DURA-CUF® Assortment Pack, Child
Includes 2 Infant, 3 Child, and 1 Small Adult Cuff
2697
ECAT
E2697J
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
Revision B
ProCare Partient Monitor Service Manual
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2-11
Product Description: 2.6. Specifications
2.6. Specifications
0 0 8 6
IPX1
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
the Medical Device Directive.
The ProCare Monitor is protected against vertically falling drops of water and conforms to
the IEC-529 standard at level IPX1. Vertically falling drops shall have no harmful effects to
the monitor.
Power Requirements
MAINS
AC INPUT VOLTAGE
Protection against electrical shock - Class II
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
Pressure Range
700 to 1060 hecto Pascal
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
2-12
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
ProCare Partient Monitor Service Manual
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Revision B
Product Description: 2.6. Specifications
Mechanical
Classification Information
Mode of Operation: Continuous degree of Protection
against harmful ingress of water: Drip-Proof IPX1.
NIBP
CUFF PRESSURE RANGE
Adult
Neonate
0 mmHg to 290 mmHg
0 mmHg to 145 mmHg
DEFAULT TARGET:
CUFF INFLATION
Adult
Neonate
150 ± 15 mmHg
110 ± 15 mmHg
TARGET CUFF INFLATION
ADJUSTMENT RANGE
Adult
Neonate
100 - 250 mmHg (5mmHg Steps)
100 - 140 mmHg (5 mmHg Steps)
BLOOD PRESSURE
DETERMINATION TIME
Adult
Neonate
120 seconds maximum
85 seconds maximum
PULSE RATE: RANGE
Adult
Neonate
30 - 200 BPM ±3%
30 - 220 BPM ±3%
BLOOD PRESSURE:
MEASUREMENT RANGES
Adult
Neonate
NIBP ACCURACY
Systolic
mmHg
MAP
mmHg
Diastolic
mmHg
30 - 290
30 - 140
20 - 260
20 - 125
10 - 220
10 - 110
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
RANGE
Max
Min
Celsius
42.2° Celsius 108.0° Fahrenheit
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
Revision B
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
Sensor Connect/Disconnect from Patient
The Monitor detects the connection or disconnection or a
sensor to the patient within 15 seconds
ProCare Partient Monitor Service Manual
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2-13
Product Description: 2.6. Specifications
SpO2 - Nellcor Pulse Oximetry
Sensor Connect/Disconnect from Monitor
The monitor detects the attachment or disconnection of a
sensor from the Monitor within 5 seconds.
Pulse Detection
The Monitor detects a pulse of enters a no-signal state
within 15 seconds of being attached to a patient.
Loss of Pulse
the monitor detects loss of pulse from patient and enters a
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
2-14
Saturation Range
1% - 100%
Pulse Rate and Accuracy
25-240 BPM ±3 digits
Perfusion Range
0.02 to 20%
ProCare Partient Monitor Service Manual
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Revision B
Product Description: 2.6. Specifications
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 cooximeter 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.
Revision B
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Product Description: 2.6. Specifications
2-16
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Revision B
3
Revision B
Principles of Operation
ProCare Patient Monitor Service Manual
2009381-001
3-1
For your notes
3-2
ProCare Patient Monitor Service Manual
2009381-001
Revision B
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.
Revsion B
ProCare Partient Monitor Service Manual
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3-3
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 NonInvasive 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.
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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 preheats 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)
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ProCare Partient Monitor Service Manual
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3-5
Principles of Operation: 3.3 Functional Description
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-of16 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.
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Revision B
Principles of Operation: 3.3 Functional Description
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.
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Principles of Operation: 3.3 Functional Description
3-8
ProCare Patient Monitor Service Manual
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Revision B
Optical Switch
Main Board
SpO2 Probe
(Optional)
SpO2 Circuit
Isolated DC
Power Supply
Temp Probe
(Optional)
Pump/Valve
Manifold
Temp Control/ Data
External DC
6V Battery
Host Comm
Port (rear)
Tubing
Control
PT1/ PT2
NIBP Data
Pneumatic
Control
UI Board
Temp
Control
Interface
Regulated
DC Power
Control / Data
RS-232
Switches
Display
LEDs
Real Time
Clock
Remote Alarm
Audio
Control
Printer Driver
Speaker
Printer
Control/
Data
BP Cuff
tubing
ProCare Vital Signs Monitor System Block Diagram (1 of 2)
page 3-9/10
Real
Time
Clock
External DC
6Volt Battery
Isolated
Power
Supply
Regulated DC
Power Supply
Printer
Drivers
Audio
Control
Speaker
Pneumatic
Valve Control
PT1/PT2
NIBP Data
SpO 2
Interface
Host
Communications
Temp Probe
(optional)
Temperature
Control/Data
Temperature
Control
ProCare Vital Signs Monitor Main Board Diagram (2 of 2)
page 3-11/12
4
Revision B
Calibration &
Maintenance
ProCare Patient Monitor Service Manual
2009381-001
4-1
For your notes
4-2
ProCare Patient Monitor Service Manual
2009381-001
Revision B
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.
Revision B
ProCare Patient Monitor Service Manual
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4-3
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
SpO2 Averaging
Window
Text in Window
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.
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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 parameterspecific 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.
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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.
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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.
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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.
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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 75.1.3.2. (Some non-USA Power bricks are equipped with a non-conductive
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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 HiPot 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
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. 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
9. Record and verify the pressure reading on the top LED display
(SYSTOLIC)
10. Record and verify the pressure reading on the bottom LED display
(DIASTOLIC)
11. Use the valve on the bulb to reduce pressure to 100mmHg
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Calibration & Maintenance: 4.6 ProCare Patient Monitor Parameter Tests
12. Record and verify the pressure reading on the top LED display
(SYSTOLIC)
13. Record and verify the pressure reading on the bottom LED display
(DIASTOLIC)
14. Use the valve on the bulb to reduce pressure to 50mmHg
15. Record and verify the pressure reading on the top LED display
(SYSTOLIC)
16. Record and verify the pressure reading on the bottom LED display
(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.
Note: To enter service mode press and hold the CYCLE button while
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
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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
Note: To enter service mode press and hold the CYCLE button while
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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Calibration & Maintenance: 4.6 ProCare Patient Monitor Parameter Tests
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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Calibration & Maintenance: 4.6 ProCare Patient Monitor Parameter Tests
5. Record and verify systolic, diastolic, map and heart rate from the monitor
display
6. Press CYCLE button until
is displayed on the HISTORY LED to
initiate a determination in STAT mode.
7. Record and verify systolic, diastolic, map and heart rate from the monitor
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
alarm sounds
is displayed on the SYSTOLIC display and an audible
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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Calibration & Maintenance: 4.6 ProCare Patient Monitor Parameter Tests
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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Calibration & Maintenance: 4.6 ProCare Patient Monitor Parameter Tests
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
Definition
Possible Cause
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.
SpO2
Alarm
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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
Alarm
4-20
Definition
Possible Cause
E63
Temp Disconnected or
Wrong Probe Type
Incorrect type of temperature probe: use
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
900999
Internal Memory Errors
Refer Monitor to Customer Service
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Calibration & Maintenance: Appendix A - Test Results Form
Appendix A - Test Results Form
Step
4.6.2
Description
Min
Max
0
6
Pressure reading at 200mmHg, top display - Systolic
197
203
Pressure reading at 200mmHg, bottom display - Diastolic
197
203
Pressure reading at 150mmHg, top display - Systolic
147
153
Pressure reading at 150mmHg, bottom display - Diastolic
147
153
Pressure reading at 100mmHg, top display - Systolic
97
103
Pressure reading at 100mmHg, bottom display - Diastolic
97
103
Pressure reading at 50mmHg, top display - Systolic
47
53
Pressure reading at 50mmHg, bottom display - Diastolic
47
53
4.6.5
Overpressure threshold, Adult (mmHg)
305
325
Overpressure threshold, Neonate (mmHg)
155
159
4.6.6
on
off
107
133
Pass-Fail-N/A
Leakage
Leakage Result (mmHg)
4.6.3
Actual
Pressure Transducer Verification
Overpressure Verification
Buttons
Software revision in systolic display (top)
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)
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Step
4.6.9
4.6.10
Description
Min
Max
Diastolic reading (mmHg)
67
93
MAP reading (mmHg)
85
95
Heart rate reading (bpm)
76
84
Systolic reading (mmHg)
107
133
Diastolic reading (mmHg)
67
93
MAP reading (mmHg)
85
95
Heart rate reading (bpm)
76
84
Systolic reading (mmHg)
107
133
Diastolic reading (mmHg)
67
93
MAP reading (mmHg)
85
95
Heart rate reading (bpm)
76
84
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
N/A
N/A
Actual
Pass-Fail-N/A
NIBP Determination (continued)
NIBP Overpressure
"E80" displayed on SYSTOLIC display
Pump will not start
Overpressure alarm can be cleared
4.6.11
Temperature reading at BP verify reads E61
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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Calibration & Maintenance: Appendix B - Connectivity
• 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.
4-24
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Calibration & Maintenance: Appendix B - Connectivity
- Apex version 2
- CIC version 3
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-25
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.
4-26
ProCare Patient Monitor Service Manual
2009381-001
Revision B
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.
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-27
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.
2.
3.
4.
5.
6.
7.
8.
9.
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
2010429-001
2010478-001
2010479-001
2010480-001
English 400 lbl kit
English 300 lbl kit
English 200 lbl kit
English 100 lbl kit
1. keypad labels set (LH & RH)
2. Fascia
3. Display cover
For language variants reference following pages
Help card guides
All 3 guides and for each language
15
16
4-28
Case, front & rear
Handle front & rear with h/w
Bulkheads 4 types & NIBP insert.
Nellcor & Masimo ‘inside’ labels
Std. labels, DC input, No temp side label.
Battery door & foam.
Help card guide and rubber feet.
Printer door (and blanking plate when available).
Cable tie hardware
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
2010429-001
Label Kit
English 400 printer
P/N (-001)
Language
Model
Is Printer Installed?
2010429-001
English
400
Printer Installed
Traditional
2010478-001
English
300
Printer Installed
Traditional
2010479-001
English
200
Printer Installed
Traditional
2010480-001
English
100
Printer Installed
Traditional
2010481-001
English
400
Printer Installed
Auscultatory
2010482-001
English
300
Printer Installed
Auscultatory
2010483-001
English
200
Printer Installed
Auscultatory
2010484-001
English
100
Printer Installed
Auscultatory
2010485-001
English
400
Traditional
2010486-001
English
300
Traditional
2010487-001
English
200
Traditional
2010488-001
English
100
Traditional
2010489-001
English
400
Auscultatory
2010490-001
English
300
Auscultatory
2010491-001
English
200
Auscultatory
2010492-001
English
100
Auscultatory
2010493-001
French
400
Printer Installed
Traditional
2010494-001
French
300
Printer Installed
Traditional
2010495-001
French
200
Printer Installed
Traditional
2010496-001
French
100
Printer Installed
Traditional
2010497-001
French
400
Printer Installed
Auscultatory
2010498-001
French
300
Printer Installed
Auscultatory
2010499-001
French
200
Printer Installed
Auscultatory
2010500-001
French
100
Printer Installed
Auscultatory
2010501-001
French
400
Traditional
2010502-001
French
300
Traditional
Revision B
Method of NIBP Determination
(Auscultatory is labeled on left keypad)
ProCare Patient Monitor Service Manual
2009381-001
4-29
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
2010503-001
French
200
Traditional
2010504-001
French
100
Traditional
P/N (-001)
Language
Model
2010505-001
French
400
Auscultatory
2010506-001
French
300
Auscultatory
2010507-001
French
200
Auscultatory
2010508-001
French
100
Auscultatory
2010509-001
German
400
Printer Installed
Traditional
2010510-001
German
300
Printer Installed
Traditional
2010511-001
German
200
Printer Installed
Traditional
2010512-001
German
100
Printer Installed
Traditional
2010513-001
German
400
Printer Installed
Auscultatory
2010514-001
German
300
Printer Installed
Auscultatory
2010515-001
German
200
Printer Installed
Auscultatory
2010516-001
German
100
Printer Installed
Auscultatory
2010517-001
German
400
Traditional
2010518-001
German
300
Traditional
2010519-001
German
200
Traditional
2010520-001
German
100
Traditional
2010521-001
German
400
Auscultatory
2010522-001
German
300
Auscultatory
2010523-001
German
200
Auscultatory
2010524-001
German
100
Auscultatory
2010525-001
Spanish
400
Printer Installed
2010526-001
Spanish
300
Printer Installed
2010527-001
Spanish
200
Printer Installed
2010528-001
Spanish
100
Printer Installed
2010529-001
Spanish
400
2010530-001
Spanish
300
2010531-001
Spanish
200
4-30
Is Printer Installed?
Method of NIBP Determination
(Auscultatory is labeled on left keypad)
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
2010532-001
Spanish
100
P/N (-001)
Language
Model
Is Printer Installed?
2010534-001
Italian
400
Printer Installed
2010535-001
Italian
300
Printer Installed
2010536-001
Italian
200
Printer Installed
2010537-001
Italian
100
Printer Installed
2010538-001
Italian
400
2010539-001
Italian
300
2010540-001
Italian
200
2010541-001
Italian
100
2010542-001
Swedish
400
Printer Installed
2010543-001
Swedish
300
Printer Installed
2010544-001
Swedish
200
Printer Installed
2010545-001
Swedish
100
Printer Installed
2010546-001
Swedish
400
2010547-001
Swedish
300
2010552-001
Swedish
200
2010553-001
Swedish
100
2010554-001
Dutch
400
Printer Installed
2010555-001
Dutch
300
Printer Installed
2010556-001
Dutch
200
Printer Installed
2010557-001
Dutch
100
Printer Installed
2010588-001
Dutch
400
2010559-001
Dutch
300
2010560-001
Dutch
200
2010561-001
Dutch
100
2010578-001
Chinese
400
Printer Installed
2010589-001
Chinese
300
Printer Installed
2010590-001
Chinese
200
Printer Installed
2010592-001
Chinese
100
Printer Installed
2010593-001
Chinese
400
Revision B
Method of NIBP Determination
(Auscultatory is labeled on left keypad)
ProCare Patient Monitor Service Manual
2009381-001
4-31
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
2010594-001
P/N (-001)
Chinese
Language
300
Model
Is Printer Installed?
2010595-001
Chinese
200
2010596-001
Chinese
100
2010597-001
Japanese
400
Printer Installed
2010598-001
Japanese
300
Printer Installed
2010599-001
Japanese
200
Printer Installed
2010600-001
Japanese
100
Printer Installed
2010601-001
Japanese
400
2010602-001
Japanese
300
2010603-001
Japanese
200
2010604-001
Japanese
100
2010605-001
Danish
400
Printer Installed
2010606-001
Danish
300
Printer Installed
2010607-001
Danish
200
Printer Installed
2010608-001
Danish
100
Printer Installed
2010609-001
Danish
400
2010610-001
Danish
300
2010611-001
Danish
200
2010612-001
Danish
100
2010613-001
Norwegian
400
Printer Installed
2010614-001
Norwegian
300
Printer Installed
2010615-001
Norwegian
200
Printer Installed
2010616-001
Norwegian
100
Printer Installed
2010617-001
Norwegian
400
2010618-001
Norwegian
300
2010619-001
Norwegian
200
2010620-001
Norwegian
100
2010621-001
Korean
400
Printer Installed
2010622-001
Korean
300
Printer Installed
2010623-001
Korean
200
Printer Installed
4-32
Method of NIBP Determination
(Auscultatory is labeled on left keypad)
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
P/N (-001)
Language
Model
Is Printer Installed?
Printer Installed
2010624-001
Korean
100
2010625-001
Korean
400
2010626-001
Korean
300
2010627-001
Korean
200
2010628-001
Korean
100
2010629-001
Finnish
400
Printer Installed
2010630-001
Finnish
300
Printer Installed
2010631-001
Finnish
200
Printer Installed
2010632-001
Finnish
100
Printer Installed
2010633-001
Finnish
400
2010634-001
Finnish
300
2010635-001
Finnish
200
2010636-001
Finnish
100
2010638-001
Portuguese
400
Printer Installed
2010639-001
Portuguese
300
Printer Installed
2010640-001
Portuguese
200
Printer Installed
2010641-001
Portuguese
100
Printer Installed
2010642-001
Portuguese
400
2010643-001
Portuguese
300
2010644-001
Portuguese
200
2010645-001
Portuguese
100
2010646-001
Russian
400
Printer Installed
2010647-001
Russian
300
Printer Installed
2010648-001
Russian
200
Printer Installed
2010649-001
Russian
100
Printer Installed
2010650-001
Russian
400
2010651-001
Russian
300
2010652-001
Russian
200
2010653-001
Russian
100
Revision B
Method of NIBP Determination
(Auscultatory is labeled on left keypad)
ProCare Patient Monitor Service Manual
2009381-001
4-33
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
P/N (-001)
Language
Model
Is Printer Installed?
2010656-001
Hungarian
400
Printer Installed
2010657-001
Hungarian
300
Printer Installed
2010658-001
Hungarian
200
Printer Installed
2010659-001
Hungarian
100
Printer Installed
2010660-001
Hungarian
400
2010661-001
Hungarian
300
2010662-001
Hungarian
200
2010663-001
Hungarian
100
2010664-001
Czech
400
Printer Installed
2010665-001
Czech
300
Printer Installed
2010666-001
Czech
200
Printer Installed
2010667-001
Czech
100
Printer Installed
2010668-001
Czech
400
2010669-001
Czech
300
2010670-001
Czech
200
2010671-001
Czech
100
2010672-001
Slovak
400
Printer Installed
2010673-001
Slovak
300
Printer Installed
2010674-001
Slovak
200
Printer Installed
2010675-001
Slovak
100
Printer Installed
2010676-001
Slovak
400
2010677-001
Slovak
300
2010678-001
Slovak
200
2010679-001
Slovak
100
2010680-001
Polish
400
Printer Installed
2010681-001
Polish
300
Printer Installed
2010682-001
Polish
200
Printer Installed
2010683-001
Polish
100
Printer Installed
2010684-001
Polish
400
4-34
Method of NIBP Determination
(Auscultatory is labeled on left keypad)
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Calibration & Maintenance: Appendix D: Replacement Parts and Assemblies
P/N (-001)
Language
Model
Is Printer Installed?
2010685-001
Polish
300
2010686-001
Polish
200
2010687-001
Polish
100
2010688-001
Greek
400
Printer Installed
2010689-001
Greek
300
Printer Installed
2010690-001
Greek
200
Printer Installed
2010691-001
Greek
100
Printer Installed
2010692-001
Greek
400
2010693-001
Greek
300
2010694-001
Greek
200
2010695-001
Greek
100
Revision B
Method of NIBP Determination
(Auscultatory is labeled on left keypad)
ProCare Patient Monitor Service Manual
2009381-001
4-35
A
Revision B
Appendix E –
Electromagnetic
Compatibility
ProCare Patient Monitor Service Manual
2009381-001
4-37
4-38
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ProCare Monitor
Electromagnetic Compatibility (EMC): ProCare
Monitor
Changes or modifications to this system not expressly approved by GE
Medical Systems can cause EMC issues with this or other equipment.
This system is designed and tested to comply with applicable regulation
regarding EMC and must be installed and put into service according to
the EMC information stated in this appendix.
WARNING
Use of portable phones or other radio frequency (RF)
emitting equipment near the system may cause
unexpected or adverse operation.
WARNING
The equipment or system should not be used adjacent to,
or stacked with, other equipment. If adjacent or stacked
use is necessary, the equipment or system should be
tested to verify normal operation in the configuration in
which it is being used.
Guidance and Manufacturer’s Declaration – Electromagnetic
Emissions
The DINAMAP® ProCare Monitor is intended for use in the
electromagnetic environment specified below. It is the responsibility of
the customer or user to assure that the DINAMAP® ProCare Monitor is
used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment – Guidance
RF Emissions
EN 55011
Group 1
The equipment uses RF energy only for its internal function. Therefore, its RF
emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
RF Emissions
EN 55011
Class B
Harmonic Emissions
EN 61000-3-2
Class A
Voltage Fluctuations/
Flicker Emissions
EN 61000-3-3
Complies
Revision B
The equipment is suitable for use in all establishments, including domestic
establishments and those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes.
ProCare Patient Monitor Service Manual
2009381-001
4-39
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ProCare Monitor
Guidance and Manufacturer’s Declaration – Electromagnetic
Immunity
The DINAMAP® ProCare Monitor is intended for use in the
electromagnetic environment specified below. It is the responsibility of
the customer or user to assure that the DINAMAP® ProCare Monitor is
used in such an environment.
Immunity Test
EN 60601 Test Level
Compliance Level
Electromagnetic Environment – Guidance
Electrostatic
Discharge (ESD)
EN 61000-4-2
± 6 kV contact
± 6 kV contact
± 8 kV air
± 8 kV air
Floors should be wood, concrete or ceramic tile. If
floors are covered with synthetic material, the relative
humidity should be at least 30%.
Electrical Fast
Transient/Burst
EN 61000-4-4
± 2 kV for power supply lines
± 2 kV for power supply
lines
Mains power should be that of a typical commercial
or hospital environment.
±1 kV for input/output lines
±1 kV for input/output
lines
Surge
EN 61000-4-5
± 1 kV differential mode
± 1 kV differential mode
± 2 kV common mode
± 2 kV common mode
<5% Ut (>95% dip in Ut)
for 0.5 cycles
<5% Ut (>95% dip in Ut)
for 0.5 cycles
<40% Ut (>60% dip in Ut)
for 5 cycles
<40% Ut (>60% dip in
Ut) for 5 cycles
<70% Ut (>30% dip in Ut)
for 25 cycles
<70% Ut (>30% dip in
Ut) for 25 cycles
<5% Ut (>95% dip in Ut)
for 5 s
<5% Ut (>95% dip in Ut)
for 5 s
3 A/m
3 A/m
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
EN 61000-4-11
Power Frequency
(50/60 Hz)
Magnetic Field
EN 61000-4-8
Mains power should be that of a typical commercial
or hospital environment.
Mains power should be that of a typical commercial
or hospital environment. If the user of the equipment
requires continued operation during power mains
interruptions, it is recommended that the equipment
be powered from an uninterruptible power supply or
a battery.
Power frequency magnetic fields should be at levels
characteristics of a typical location in a typical
commercial or hospital environment.
NOTE:
Ut is the AC mains voltage prior to application of the test level.
4-40
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ProCare Monitor
Guidance and Manufacturer’s Declaration – Electromagnetic
Immunity
The DINAMAP® ProCare Monitor is intended for use in the
electromagnetic environment specified below. It is the responsibility of
the customer or user to assure that the DINAMAP® ProCare Monitor is
used in such an environment.
Immunity Test
EN 60601 Test Level
Compliance Level
Electromagnetic Environment – Guidance
Portable and mobile RF communications equipment should not
be used closer to any part of the equipment, including cables,
than the recommended separation distance calculated from the
equation applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
EN 61000-4-6
3 Vrms
150 KHz to 80 MHz
3 V rms
Radiated RF
EN 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
d = 1.2
P
d = 1.2
P 80 MHz to 800 MHz
d = 2.3
P 800 MHz to 2.5 GHz
where P is the maximum output power rating of the transmitter
in watts (W) according to the transmitter manufacturer, and d is
the recommended separation distance in meters (m).
Field strengths from fixed RF transmitters, as determined by an
electromagnetic site surveya, should be less than the
compliance level in each frequency rangeb.
Interference may occur in the vicinity of equipment marked with
the following symbol:
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by reflection from structures, objects,
and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radio,
AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the equipment is used exceeds the applicable RF compliance level above,
the equipment should be observed to verify normal operation. If abnormal performance is observed, additional measures
may be necessary, such as re-orienting or relocating the equipment.
bOver the frequency range 150 KHz to 80 MHz, field strengths should be less than 3 V/m.
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-41
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ProCare Monitor
Recommended Separation Distances
The table below provides the recommended separation distances (in
meters) between portable and mobile RF communications equipment and
the DINAMAP® ProCare Monitor.
The DINAMAP® ProCare Monitor is intended for use in the
electromagnetic environment on which radiated RF disturbances are
controlled. The customer or the user of the DINAMAP® ProCare Monitor
can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications
equipment (transmitters) and the DINAMAP® ProCare Monitor as
recommended below, according to the maximum output power of the
communications equipment.
Separation Distance in Meters (m) According to Frequency of Transmitter
Rated Maximum Output
Power of Transmitter in
Watts
150 kHz to 80 MHz a
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
a
d = 1.2
P
80 MHz to 800 MHz a
d = 1.2
P
800 MHz to 2.5 GHz a
d = 2.3
P
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
For transmitters rated at a maximum output power not listed above, the
recommended separation distance [d] in meters (m) can be estimated
using the equitation applicable to the frequency of the transmitter,
where P is the maximum output power rating of the transmitter in watts
(W) according to the transmitter manufacturer.
NOTE:
These guidelines may not apply in all instances. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects and people.
4-42
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ProCare Monitor
Compliant Cables and Accessories
WARNING
The use of accessories, transducers and cables other than
those specified may result in increased emissions or
decreased immunity performance of the equipment or
system.
The table below lists cables, transducers, and other applicable
accessories with which GE Medical Systems claims EMC compliance.
NOTE: Any supplied accessories that do not affect EMC compliance are
not included.
Part No
Description
Maximum Lengths
2008774-001
Turbo-Temp Oral Probe, Blue
3.0 m / 10 ft
2008775-001
Turbo-Temp Rectal Probe, Red
3.6 m / 12 ft
2016998-001
Dual Temp Cable
20 cm / 8 in
407705-006
Nellcor DuraSensor Reusable Finger Probe
(DS100A)
0.9 m/ 3 ft
2008773-001
Nellcor Interface Cable, OxiSmart, DOC 10 Cable
3.3 m / 11 ft
2009743-001
Masimo PC08 Cable
2.5 m / 8.2 ft
2009745-001
Masimo Finger Sensor, Adult, Reusable
N/A
316579-001
AC Cable, Hospital Grade, AHA
3.6 m / 12 ft
2013057-001
Universal AC/DC Adapter
N/A
ILC-1926
Isolated Level Converter
N/A
Temperature Cables and Probes
Pulse Oximetry Cables and Sensors
Accessories
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-43
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1926
Electromagnetic Compatibility (EMC): ILC-1926
Changes or modifications to this system not expressly approved by GE
Medical Systems can cause EMC issues with this or other equipment.
This system is designed and tested to comply with applicable regulation
regarding EMC and must be installed and put into service according to
the EMC information stated in this appendix.
WARNING
Use of portable phones or other radio frequency (RF)
emitting equipment near the system may cause
unexpected or adverse operation.
WARNING
The equipment or system should not be used adjacent to,
or stacked with, other equipment. If adjacent or stacked
use is necessary, the equipment or system should be
tested to verify normal operation in the configuration in
which it is being used.
Guidance and Manufacturer’s Declaration – Electromagnetic
Emissions
The ILC-1926 is intended for use in the electromagnetic environment
specified below. It is the responsibility of the customer or user to assure
that the ILC-1926 is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment – Guidance
RF Emissions
EN 55011
Group 1
The equipment uses RF energy only for its internal function. Therefore, its RF
emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
RF Emissions
EN 55011
Class B
Harmonic Emissions
EN 61000-3-2
Not Applicable
Voltage Fluctuations/
Flicker Emissions
EN 61000-3-3
Complies
4-44
The equipment is suitable for use in all establishments, including domestic
establishments and those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes.
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1926
Guidance and Manufacturer’s Declaration – Electromagnetic
Immunity
The ILC-1926 is intended for use in the electromagnetic environment
specified below. It is the responsibility of the customer or user to assure
that the ILC-1926 is used in such an environment.
Immunity Test
EN 60601 Test Level
Compliance Level
Electromagnetic Environment – Guidance
Electrostatic
Discharge (ESD)
EN 61000-4-2
± 6 kV contact
± 6 kV contact
± 8 kV air
± 8 kV air
Floors should be wood, concrete or ceramic tile. If
floors are covered with synthetic material, the relative
humidity should be at least 30%.
Electrical Fast
Transient/Burst
EN 61000-4-4
± 2 kV for power supply lines
No AC Input
No AC Input
Surge
EN 61000-4-5
± 1 kV differential mode
No AC Input
Mains power should be that of a typical commercial
or hospital environment.
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
EN 61000-4-11
Power Frequency
(50/60 Hz)
Magnetic Field
EN 61000-4-8
±1 kV for input/output lines
± 2 kV common mode
<5% Ut (>95% dip in Ut)
for 0.5 cycles
<5% Ut (>95% dip in Ut)
for 0.5 cycles
<40% Ut (>60% dip in Ut)
for 5 cycles
<40% Ut (>60% dip in
Ut) for 5 cycles
<70% Ut (>30% dip in Ut)
for 25 cycles
<70% Ut (>30% dip in
Ut) for 25 cycles
<5% Ut (>95% dip in Ut)
for 5 s
<5% Ut (>95% dip in Ut)
for 5 s
3 A/m
3 A/m
Mains power should be that of a typical commercial
or hospital environment. If the user of the DINAMAP
ILC-1926 requires continued operation during power
mains interruptions, it is recommended that the Host
monitor be powered from an uninterruptible power
supply or a battery.
Power frequency magnetic fields should be at levels
characteristics of a typical location in a typical
commercial or hospital environment.
NOTE:
Ut is the AC mains voltage prior to application of the test level.
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-45
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1926
Guidance and Manufacturer’s Declaration – Electromagnetic
Immunity
The ILC-1926 is intended for use in the electromagnetic environment
specified below. It is the responsibility of the customer or user to assure
that the ILC-1926 is used in such an environment.
Immunity Test
EN 60601 Test Level
Compliance Level
Electromagnetic Environment – Guidance
Portable and mobile RF communications equipment should not
be used closer to any part of the equipment, including cables,
than the recommended separation distance calculated from the
equation applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
EN 61000-4-6
3 Vrms
150 KHz to 80 MHz
3 V rms
Radiated RF
EN 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
d = 1.2
P
d = 1.2
P 80 MHz to 800 MHz
d = 2.3
P 800 MHz to 2.5 GHz
where P is the maximum output power rating of the transmitter
in watts (W) according to the transmitter manufacturer, and d is
the recommended separation distance in meters (m).
Field strengths from fixed RF transmitters, as determined by an
electromagnetic site surveya, should be less than the
compliance level in each frequency rangeb.
Interference may occur in the vicinity of equipment marked with
the following symbol:
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by reflection from structures, objects,
and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radio,
AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the equipment is used exceeds the applicable RF compliance level above,
the equipment should be observed to verify normal operation. If abnormal performance is observed, additional measures
may be necessary, such as re-orienting or relocating the equipment.
bOver the frequency range 150 KHz to 80 MHz, field strengths should be less than 3 V/m.
4-46
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1926
Recommended Separation Distances
The table below provides the recommended separation distances (in
meters) between portable and mobile RF communications equipment and
the ILC-1926.
The ILC-1926 is intended for use in the electromagnetic environment on
which radiated RF disturbances are controlled. The customer or the user
of the ILC-1926 can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the ILC-1926 as
recommended below, according to the maximum output power of the
communications equipment.
Separation Distance in Meters (m) According to Frequency of Transmitter
Rated Maximum Output
Power of Transmitter in
Watts
150 kHz to 80 MHz a
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
a
d = 1.2
P
80 MHz to 800 MHz a
d = 1.2
P
800 MHz to 2.5 GHz a
d = 2.3
P
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
For transmitters rated at a maximum output power not listed above, the
recommended separation distance [d] in meters (m) can be estimated
using the equitation applicable to the frequency of the transmitter,
where P is the maximum output power rating of the transmitter in watts
(W) according to the transmitter manufacturer.
NOTE:
These guidelines may not apply in all instances. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects and people.
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-47
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1926
Compliant Cables and Accessories
WARNING
The use of accessories, transducers and cables other than
those specified may result in increased emissions or
decreased immunity performance of the equipment or
system.
The table below lists cables, transducers, and other applicable
accessories with which GE Medical Systems claims EMC compliance.
NOTE: Any supplied accessories that do not affect EMC compliance are
not included.
Part No
Description
Maximum Lengths
N/A
RJ45 series Category 5 cable
N/A
683235
Adapter Cable, RJ45 to DB15.
600 mm / 2 ft
683236
Adapter Cable, RJ45 to DB25
460 mm / 18 in
683242
Adapter Cable, RJ45 to DB9.
3.0 m / 10 ft
Accessories
4-48
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1931
Electromagnetic Compatibility (EMC): ILC-1931
Changes or modifications to this system not expressly approved by GE
Medical Systems can cause EMC issues with this or other equipment.
This system is designed and tested to comply with applicable regulation
regarding EMC and must be installed and put into service according to
the EMC information stated in this appendix.
WARNING
Use of portable phones or other radio frequency (RF)
emitting equipment near the system may cause
unexpected or adverse operation.
WARNING
The equipment or system should not be used adjacent to,
or stacked with, other equipment. If adjacent or stacked
use is necessary, the equipment or system should be
tested to verify normal operation in the configuration in
which it is being used.
Guidance and Manufacturer’s Declaration – Electromagnetic
Emissions
The ILC-1931 is intended for use in the electromagnetic environment
specified below. It is the responsibility of the customer or user to assure
that the ILC-1931 is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment – Guidance
RF Emissions
EN 55011
Group 1
The equipment uses RF energy only for its internal function. Therefore, its RF
emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
RF Emissions
EN 55011
Class A
Harmonic Emissions
EN 61000-3-2
Not Applicable
Voltage Fluctuations/
Flicker Emissions
EN 61000-3-3
Not Applicable
Revision B
The equipment is suitable for use in all establishments other than domestic and
those directly connected to the public low-voltage power supply network that
supplies buildings used for domestic purposes.
ProCare Patient Monitor Service Manual
2009381-001
4-49
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1931
Guidance and Manufacturer’s Declaration – Electromagnetic
Immunity
The ILC-1931 is intended for use in the electromagnetic environment
specified below. It is the responsibility of the customer or user to assure
that the ILC-1931 is used in such an environment.
Immunity Test
EN 60601 Test Level
Compliance Level
Electromagnetic Environment – Guidance
Electrostatic
Discharge (ESD)
EN 61000-4-2
± 6 kV contact
± 6 kV contact
± 8 kV air
± 8 kV air
Floors should be wood, concrete or ceramic tile. If
floors are covered with synthetic material, the relative
humidity should be at least 30%.
Electrical Fast
Transient/Burst
EN 61000-4-4
± 2 kV for power supply lines
N/A
No AC Input
Surge
EN 61000-4-5
± 1 kV differential mode
N/A
No AC Input
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
EN 61000-4-11
Power Frequency
(50/60 Hz)
Magnetic Field
EN 61000-4-8
±1 kV for input/output lines
± 2 kV common mode
<5% Ut (>95% dip in Ut)
for 0.5 cycles
<5% Ut (>95% dip in Ut)
for 0.5 cycles
<40% Ut (>60% dip in Ut)
for 5 cycles
<40% Ut (>60% dip in
Ut) for 5 cycles
<70% Ut (>30% dip in Ut)
for 25 cycles
<70% Ut (>30% dip in
Ut) for 25 cycles
<5% Ut (>95% dip in Ut)
for 5 s
<5% Ut (>95% dip in Ut)
for 5 s
3 A/m
3 A/m
Mains power should be that of a typical commercial
or hospital environment. If the user of the ILC-1931
requires continued operation during power mains
interruptions, it is recommended that the Host
monitor be powered from an uninterruptible power
supply or a battery.
Power frequency magnetic fields should be at levels
characteristics of a typical location in a typical
commercial or hospital environment.
NOTE:
Ut is the AC mains voltage prior to application of the test level.
4-50
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1931
Guidance and Manufacturer’s Declaration – Electromagnetic
Immunity
The ILC-1931 is intended for use in the electromagnetic environment
specified below. It is the responsibility of the customer or user to assure
that the ILC-1931 is used in such an environment.
Immunity Test
EN 60601 Test Level
Compliance Level
Electromagnetic Environment – Guidance
Portable and mobile RF communications equipment should not
be used closer to any part of the equipment, including cables,
than the recommended separation distance calculated from the
equation applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
EN 61000-4-6
3 Vrms
150 KHz to 80 MHz
3 V rms
Radiated RF
EN 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
d = 1.2
P
d = 1.2
P 80 MHz to 800 MHz
d = 2.3
P 800 MHz to 2.5 GHz
where P is the maximum output power rating of the transmitter
in watts (W) according to the transmitter manufacturer, and d is
the recommended separation distance in meters (m).
Field strengths from fixed RF transmitters, as determined by an
electromagnetic site surveya, should be less than the
compliance level in each frequency rangeb.
Interference may occur in the vicinity of equipment marked with
the following symbol:
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by reflection from structures, objects,
and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radio,
AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the equipment is used exceeds the applicable RF compliance level above,
the equipment should be observed to verify normal operation. If abnormal performance is observed, additional measures
may be necessary, such as re-orienting or relocating the equipment.
bOver the frequency range 150 KHz to 80 MHz, field strengths should be less than 3 V/m.
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-51
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1931
Recommended Separation Distances
The table below provides the recommended separation distances (in
meters) between portable and mobile RF communications equipment and
the ILC-1931.
The ILC-1931 is intended for use in the electromagnetic environment on
which radiated RF disturbances are controlled. The customer or the user
of the ILC-1931 can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the ILC-1931 as
recommended below, according to the maximum output power of the
communications equipment.
Separation Distance in Meters (m) According to Frequency of Transmitter
Rated Maximum Output
Power of Transmitter in
Watts
150 kHz to 80 MHz a
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
a
d = 1.2
P
80 MHz to 800 MHz a
d = 1.2
P
800 MHz to 2.5 GHz a
d = 2.3
P
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
For transmitters rated at a maximum output power not listed above, the
recommended separation distance [d] in meters (m) can be estimated
using the equitation applicable to the frequency of the transmitter,
where P is the maximum output power rating of the transmitter in watts
(W) according to the transmitter manufacturer.
NOTE:
These guidelines may not apply in all instances. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects and people.
4-52
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1931
Compliant Cables and Accessories
WARNING
The use of accessories, transducers and cables other than
those specified may result in increased emissions or
decreased immunity performance of the equipment or
system.
The table below lists cables, transducers, and other applicable
accessories with which GE Medical Systems claims EMC compliance.
NOTE: Any supplied accessories that do not affect EMC compliance are
not included.
Part No
Description
Maximum Lengths
683235
Adapter Cable, RJ45 to DB15
600 mm / 2 ft
418497-002
Apex Pro Cable
1.8m / 6 ft
Accessories
Revision B
ProCare Patient Monitor Service Manual
2009381-001
4-53
Appendix E – Electromagnetic Compatibility: Electromagnetic Compatibility (EMC): ILC-1931
4-54
ProCare Patient Monitor Service Manual
2009381-001
Revision B
Assembly Drawings & ProCare Schematics: Appendix D: Replacement Parts and Assemblies
5
Assembly Drawings &
ProCare Schematics
ProCare Patient Monitor Service Manual
2009381-001
Revision B
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
C50
C45
100nF 25V
C48
25V 100nF
100nF 25V
C44
C46
P3V3 P3V3
100nF 25V
100nF 25V
R1
R117
100K 100K
100nF 25V
10K0
P3V3
R108
1K00
T_DE
T_CLK
T_TDI
T_TDO
T_TMS
T_TRST
75R0
R201
TP26
75R0
99
92
93
94
95
98
C32
10P
0R0
C33
10P
R90
RESET_PRI-0
P3V3
R120
R62
10M0
XL2
8.0MHZ
1K00
R115100K
100K
ADC_PWM
CS_DISPLAY
PWM_VOL
PWM_PITCH
59
70
82
81
52
51
85
88
64
44
P5D
C12
10N0
C49
100NF
25V
P5D
C1
10U0
P3V3
C14
10N0
C52
100NF
25V
C15
10N0
P5A
C2
10U0
P3V3
C53
100NF
25V
C3
10U0
C16
10N0
VDD5
VDD4
VDD3
PB0
PB1
PB2
PB3
PB4
PB5
PB6
PB7
DE
TCLK
TDI
TDO
TMS
TRST
90
CLKOUT
87
EXTAL
86
XTAL
83
RESET
84
RSTOUT
43
ICOC10
42
ICOC11
41
ICOC12
40
ICOC13
39
ICOC20
38
ICOC21
37
ICOC22
36
ICOC23
R63
1K00
C54
P3V3SEC
100NF
25V
VPP
VDDH
VDDA
VSSA
VDDF
VSSF
VDDSYN
VSSSYN
VSTBY
TEST
R95
1K00
R104
1K00
49
50
53
56
57
58
60
61
PUMP_ON
DUMP_ON
LATCHED_OVP
DUMP2_ON
ADULT-0
PNEU_RESET
R116
TP34
TP33
100K
7
PA0
6
PA1
5
PA2
4
PA3
3
PA4
2
PA5
1
PA6
100
PA7
63
MISO
62
MOSI
65
SCK
66
SS
R206
Place near U9
R103
RESET_TEST-0
U9
MMC2107
PC0
PC1
PC2
PC3
PC4
PC5
PC6
PC7
PD0
PD1
PD2
PD3
PD4
PD5
PD6
PD7
PR_DI
PR_CLK
PR_ST1
PR_ST2
PR_ST3
PR_ST4
PR_ST5
PR_ST6
17
16
15
14
11
10
9
8
12
21
54
89
96
PR_VHON
PR_M4
PR_M2
PR_M3
PR_M1
PR_EOP_EN
PR_LAT
PR_EOP
1K00
27
26
25
24
23
20
19
18
R114
SHDN_TO_PRI
1K00
SW_MUX
RTC_DATA
R113
TP42
RTC_CLK
SPO2_RST-0
IPS_ON
CS_SEC-0
R112
1K00
35
34
33
32
31
30
29
28
FSP_FROM_PRI
FAST_OVP-0
DUMP_ON_MON
D_FROM_TEMP
D_TO_TEMP
REM_ALARM-0
TEMP_PROBE_IN
DUMP2_ON_MON
R107
69
PE5
68
PE6
67
PE7
VSS5
R106
TP39 TP40 TP41
97
INT0
INT1
INT2
INT3
INT4
INT5
INT6
INT7
VSS4
SPI_MISO
SPI_MOSI
SPI_CLK
91
80
VRH
79
VRL
48
RXD1
46
RXD2
47
TXD1
45
TXD2
1K00
R119
D_FROM_COMM
D_FROM_SPO2
D_TO_COMM
D_TO_SPO2
55
VSS3
1K00
PQA0
PQA1
PQA3
PQA4
PQB0
PQB1
PQB2
PQB3
VSS2
V_DC_MON
PUMP_I
PT1
PT2
FPT
V_BAT_MON_PRI
VSS1
I_CHG
78
77
76
75
74
73
72
71
22
VDD2
R84
VDD1
13
PR_TH
R98 P3V3
10K0
FSP_TO_PRI
1K00
TP30
R118
100K
R190
10K0
PE7 needs to be high at start-up
C5
100NF
25V
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(1 of 10) page 5-5/6
+3.3V SECONDARY POWER
PBAT
P3V3SEC
C141
100nF 25V
16 VCC
C115
R137
10K0
R141
49K9
P3V3SEC
RESET
U27
9 OSCOUT2
100nF 25V
10 OSCOUT1
11 OSCIN
12 RESET
8 GND
Q14
Q13
Q12
Q10
Q9
Q8
Q7
Q6
Q5
Q4
3
2
1
15
13
14
6
4
5
7
1
VIN
C106
2U2 C13
10N0
16V
Q14
DTC143ZKA
Logic
U22
3
ON/OFFL LP2985
4
BYPASS
VOUT
GND
2
C56
SECONDARY PROCESSOR
P3V3SEC
R174
10K2
P3V3SEC
2
3
4
5
6
TP1
C35
C34
22P0
C103
12P0
XL3
32.768KHZ
1 OSCI
8
VDD
R3
4K99
CLKOUT 7
2 OSCO
SCL 6
RTC_CLK
3 INT
SDA 5
RTC_DATA
VSS
4
20
VDD
RA0/AN0
RA1/AN1
RA2/AN2
RA3/AN3/VREF
RA4
R175
10K2
9 OSC1
XL1
4.0MHZ
R37
1K00
R2
4K99
100nF 25V
1 MCLR
22P0
U21
PCF8563T
P3V3SEC
C55
R43
1K00
R176
20K0
FSP_TO_PRI
SEC_ALARM
P3V3
25V 100nF
PT2_SEC
R177
20K0
REAL TIME CLOCK
C105
10U0
P3V3SEC
74LV4060
V_BAT_MON_SEC
I_CHG
P5A2
5
R35
0R0
10
RB7
RB6
RB5
RB4
RB3
RB2
RB1
RB0/INT0
28
27
26
25
24
23
22
21
FAST_CHG
LATCHED_OVP
FAST_OVP-0
PNEU_OVERRIDE-0
RESET_PRI-0
SW_PWR-0
U3
PIC16LC73B
OSC2
RC0 11
12 RC1/CCP2
13
RC2/CCP1
RC7/RX
RC6/TX
RC5/SDO
RC4/SDI
RC3/SCK
RA5/AN4/SS
AGND
8
18
17
16
15
14
7
VSS
19
FSP_FROM_PRI
PNEU_RESET
ADULT-0
SPI_MOSI
SPI_CLK
CS_SEC-0
SHDN_TO_PRI
PS_ON
SPI_MISO
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(2 of 10) page 5-7/8
P6VMIN
C66
P5A
100nF 25V
1 VIN
Pump Connector
P5D
PBAT
P5D
C39
J7
1
2
3
4
5
6
220U0
PBAT
PUMP
P5D
DUMP
P5D
DUMP2
PBAT
3
1
3 ON/OFF
U7
VOUT 5
C37
2U2
GND
2
16V
D9
BAS16
C28
33U0
1
25V
3
25V
3
1
TP38
TP37
C65
100nF 25V
P5D
C140
33U0
PNEUMATICS
LP2980-5V
PBACK_IN
PBACK_OUT
XFPM-050
PT1
5V1
D1
3
VCC
VOUT
GND
CAP
3
D10
BAS16
1
2
1
R180
6
C20
R36
R51
0R0
2K0
PT1
C67
100NF
25V
1K00 680P
D27
BAS16
Spare Parts
DUMP_ON_MON
R202
3
100K
Q7
5
SI2306DS
DUMP_ON
3
9
2
DUMP2_ON_MON R203
11
Q24
SI2306DS
DUMP2_ON
3
13
1
R204
100K
R205
100K
R173
100K
U14
HCT04
P5A
4
R9
10K0
6
U14
HCT04
C60
100nF 25V
U14
HCT04
U14
HCT04
3
R10
8
2
10K0
U13
8
FPT
1
4
10
R6
10K0
C17
10N0
12
R83
649K
C64
2
R121
100K
10N0
Q17
PNEU_OVERRIDE-0
P5A
TLC2272
1
100K
U14
HCT04
R29
4K99
SI2306DS
3
P6VMIN
1
2
Q9
SI9410DY
PUMP_ON
6
100nF 25V
7
2
1 VIN
3
Q8
SI9410DY
FAST_OVP-0
4
6
7
R100
10K0
U6
GND
1
ADC_PWM
U14
7
GND
2
VOUT 5
C36
2U2
16V
R44
1K00
3
R99
10K0
4K99
HCT04
8
2
R5
10K0
2
LP2980-5V
3 ON/OFF
5
100nF 25V
C43
470N
P5A2
8
4
C61
VCC 14
R28
C58
5
P5A
R75
0R10
C63
C59
100NF
25V
100nF 25V
XFPM-050
PT2
VCC
PUMP_I
3
GND
2
1
CAP
6
VOUT
PT2
R50
R181
C21
1K00
680P
2K0
C57
100NF
25V
PT2_SEC
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(3 of 10) page 5-9/10
BATTERY CHARGER
DC Input Power
V_IN
J3
1
2
3
C104
100nF
FS1
L4
2A5
900NH_0A7
2
D5
PBAT
MIC4681-ADJ
2 VIN
1
BYG22
1
R96
301K
2
D8
C69
C29
33U0
SM6T39CA
1 SHDN
100nF
5
25V
1
SW 3
U17
FB 4
GND
6
7
8
1
2
D4
BYS10
68U0
L1
2
2
D3
1
BYG22
C70
C40
220U0
100NF
25V
25V
R25
49K9
V_DC_MON
C90
R87
100K
100nF
BC_5V
8
MC78L05
IN
R149
0R10
U2
OUT
GND
2 3 6 7
R39
301K
PBAT
1
C68
VR1
50K
100NF
25V
CW
VF = 6.9 V
VC = 7.2 V
R150
0R10
R42
10K0
BC_5V
Battery Connector
PBAT
J2
1
C71
R13
10K0
4A0
FS4
100nF 25V
3
MBR2030CTL
3
D14
25V
1
C98
33U0
2
2
2
R11
R138
5
10K0
R92
100K
R147
100K
R76
0R10
10K0
OPA2340
U15
V = 0.191 V @ 75mA
R182
0R10
8 OPA2340
1
4
R72
4K99
1
D12
3
BAS16
R81
200K
C116
7
6
U15
100nF 25V
R148
150K
R61
R93
49K9
C91
100NF
25V
R146
100K
249K
C117
C118
100NF
25V
100nF 25V
Q15
DTC143ZKA
Logic
R64
4K99
V_BAT_MON_SEC
V_BAT_MON_PRI
I_CHG
FAST_CHG
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(4 of 10) page 5-11/12
+3.3 V SUPPLY
PBAT
P3V3
MIC4680-3V3
2 VIN
C30
33U0
R101
10K0
25V
U12
1 SHDN
C74
100NF
25V
GND
6
7
5
1
SW 3
Q12
C41
220U0
C75
100NF
25V
25V
D6
BYG22
ANALOG VOLTAGE SUPPLY (+6.5 V)
SI2307DS
Logic
2
8
1
Q18
DTC143ZKA
L2
FB 4
2
PS_ON
68U0
2
1
1
3
5 VIN
C31
33U0
25V
C93
100NF
25V
68U0
MIC3172
U16
4 EN
L3
2
P6VMIN
VSW 7
1
BYG22
FB 3
GND COMP
8 6
2
SGND
1
D7
2
R27
12K1
R65
1K00
C96
220U0
25V
C97
220U0
25V
C76
100NF
25V
R33
2K87
C25
1U0
16V
PROGRAM CONNECTOR
J1
1
PGM_PS_ON-0
2
3
4
+5.0 V SUPPLY
5
2 VIN
C38
2U2
16V
C72
100NF
25V
P5D
MIC39101-5V
1 EN
5 6
U5
GND
VOUT 3
FLG 4
7 8
C73
100NF
25V
C4
10U0
RESET_TEST-0
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(5 of 10) page 5-13/14
P3V3
R123 R59
100K 100K
R58
100K
R57
100K
R56
10K0
R55
100K
R54
100K
R122
100K
100nF 25V
20
19
VCC 2OE
2
1A0
4
1A1
6
1A2
8
1A3
17
2A0
15
2A1
13
2A2
11
2A3
PR_DI
PR_ST6
PR_ST5
PR_ST4
PR_ST3
PR_ST2
PR_ST1
PR_CLK
U11 1Y0 18
16
1Y1
14
1Y2
12
1Y3
3
2Y0
5
2Y1
7
2Y2
9
2Y3
HCT240
1OE
1
P5A
R97
1M00
PR_EOP
7
P3V3
8
4
Q11
P5D
R60
30K1
R91
20K0
TLC2272
GND
10
P5A
P5A
PR_EOP_EN
PRINTER INTERFACE
P5D
C79
Printer Connector
J9
5
1
2
6
3
4
R89
30K1
U13
5
6
7
DTA143XKA
Logic
8
R73
9
10
100R
PBAT
11
12
13
14
R14
10K0
15
Q5
16
SI2307DS
R15
17
2
18
1
PBAT_PR
10K0
19
20
3
21
PR_VHON
C6
33U0
Q3
DTC143ZKA
22
25V
Logic
23
P5A
24
25
26
R26
15K0
27
PR_TH
P5D
R53
2K0
PR_LAT
Q4
DTC143ZKA
C77
Logic
C78
P3V3
100nF 25V
25V 100nF
2 13 5
VCC VS2 VS1
3 IN1
OUT1 4
PR_M1
PR_M3
PR_M2
PR_M4
7 IN2
15 IN3
LB1831M
U4
OUT2 6
OUT3 14
11 IN4
OUT4 12
17
19
FG7
FG5
18
20
FG6
FG8
FG1 FG2 FG3 FG4
1 8
9 16
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(6 of 10) page 5-15/16
AUDIO ALARMS
P5D
R49
1R00
P5D
PWM_VOL
3 C
R82
10K0
C7
10U0
Q27
MMBT3904LT1
1
B
16V
E 2
C26
1U0
R24
100K
16V
1
D18
R41
10N0
4K99
U10
LM386
3
6
1
2
C11
10N0
R111
10K0
PWM_PITCH
C10
C87
R71
15K0
100NF
25V
4
8
7
5
C8
10U0
3
R94
49K9
C88
100NF
25V
R46
P5D
1K00
P5D
R179
2K0
3
1
Q26
Logic
HOST COMM
1
P5D
C85
Logic
3
D16
5V1
P5D
Q28
DTC143ZKA
Logic
100nF 25V
2 C1+
C83
100NF
25V
15
VCC
4 C15 C2+
C82
100NF
25V
12
16
FON FOFF
U8
ICL3221
V- 7
6 C211 T1IN
9
P5D
Comms Connector
C84
GND
1
TTL_TX
2
J6
TTL_RX 3
100nF 25V
5V_FUSED 4
GND 5
REMOTE_ALARM-0 6
C81
RS-232_TX 7
RS-232_RX 8
100nF 25V
T1OUT 13
External DB15
Connector Mapping
R1IN 8
R1OUT
1 EN
D_FROM_COMM
V+ 3
FS2
DTC143ZKA
DTC143ZKA
D15
5V1
0A3
D_TO_COMM
Q25
Speaker Connector
100NF
25V
R124
10K0
10N0
R178
1K00
2
P5D
C89
SEC_ALARM
1
220U0
R74
2R70
C86
16V
BAS16
J4
C42
1 INVALID
J6
0
1
2
3
4
5
6
7
8
GND
14
FS3
0A3
Q13
DTA143XKA
Logic
R110
10K0
Q6
NDT3055L
1
REM_ALARM-0
2
NAME
GND
TTL_TX
TTL_RX
5V_FUSED
GND
REMOTE_ALARM-0
RS-232_TX
RS-232_RX
DB15
1
2
3
4
7
8
11
13
D2
SM6T15CA
R102
10K0
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(7 of 10) page 5-17/18
Test Connector
P3V3
R19
10K0
R22
10K0
R18
10K0
C92
R17
10K0
100NF
25V
T_TDI
1
T_TDO
3
T_CLK
5
P3V3
J10
2
P5D
PBAT
Display Connector
R125
10K0
4
6
7
RESET_TEST-0
T_TMS
8
1
9
2
SW_MUX
10
11
T_DE
12
T_TRST
14
3
4
CS_DISPLAY
SW_PWR-0
SPI_MOSI
SPI_CLK
13
R21
1K00
J5
5
6
7
8
V_IN
R133
R134
R135
499
499
499
9
CHARGING_LED 10
R126
100K
R127
100K
ISOLATED POWER SUPPLY
D19
L12
C147
330P
R200
150
2
MCB1608S102E
2 VIN
1
BYG22
C148
C122
10U0
1 EN
100NF
25V
P5TEMP
MIC39101-5V
5 6
U29
GND
VOUT 3
C121
10U0
FLG 4
7 8
T
PBAT
SP
D21
1
R185
4K99
C124
10U0
C126
10U0
C149
MIC5270-5.0
100NF
25V
2 GND
5 -VIN
2
U28-VOUT
SP
C129
33U0
C151
25V
R153
75R0
12
IPS_ON
15 SD-0
SW 11
6 SYNC
C127
1N0
PKG_TYPE=0603
VIN
R152
3K01
FB 3
4 VC
ROC 14
5 RREF
RCC 13
R151
D20
7
2
2
L11
8
11
L13
MCB1608S102E
5
MMZ2012R102A
DO NOT POPULATE
P5VSP
T1
6395-TO12
C128
680P
N5VSP
4
BYG22
100NF
25V
ISOLATION BARRIER
2 VIN
1
BYG22
C123
10U0
C150
100NF
25V
MIC39101-5V
1 EN
5 6
U30
GND
VOUT 3
FLG 4
C125
10U0
7 8
12
13K7
0.1%
SP
LT1425CS
U31
9 G3
G1 1
16 G4
G2 8
7 SG
PG 10
C101
C102
1N0
1N0
C145
C146
1N0
1N0
3K15V
3K15V
3K15V
3K15V
ISOLATION BARRIER
SCHEMATIC
SP
T
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(8 of 10) page 5-19/20
SpO2 Module Connector 10 pin
1
1
2
J8
8
1
7
3
6
4
5
2
6
7
8
9
6
7
GND
3
8
N/C
10
N/C
11
LED +
2
13
3
14
4
FL2
INNER SHIELD
INNER SHIELD
DET ANODE
DET CATHODE
LED -
RED LED CATHODE
RCAL
10
DIGICAL
11
12
1
13
Z>200/100MHZ
NC
12
GND
FL1
4
9
LED -
IR LED CATHODE
5
5
DET - C
MASIMO
LED +
4
4
DIGICAL
NELLCOR
RCAL - RETURN
3
Z>200/100MHZ
3
GND
TO J1 ON NELLCOR MP506
FL3
2
J11
DET + A
SpO2 Patient Connector
Allow 4mm clearance between these signal and all other board signals
14
15
ANALOG GND
OUTER SHIELD
DET CATHODE
DET ANODE
16
2
1
Z>200/100MHZ
J16
DET + A
INNER SHIELD
INNER SHIELD
TO J1 ON MASIMO MS-5
1
2
DET - C
N/C
OUTER SHIELD
IR LED CATH
OUTER SHIELD
RED LED CATH
N/C
P5VSP
3
4
5
6
NC
2
7
D35
8
9
10
BAV199
3
NC
1
P5VSP
P3V3
Q19
P3V3
Logic
R144
249
R183
10K0
U23
4N35
DTA143XKA
1
2
AN
C
B
CTH
E
SP
SpO2 Module Connector 14 pin
5
6
4
N5VSP P5VSP
R129
10K0
SP
C119
100nF 25V
SPO2_RST-0
J12
P5VSP
P5D
1
8
7
6
5
VCC
AN
VE
VO
GND
CTH
GND
4
2
3
C 3
Q16
MMBT3904LT1
1
B
RESET
5
R142
3K01
GND
6
+12V (N/A)
7
ANALOG OUT (N/A)
8
TRANSMIT (MP506 OUT)
9
RECEIVE (MP506 IN)
10
2 E
11
R136
499
P5VSP
P3V3
CTS (MP506 IN)
Q20
Logic
R145
249
2
3
AN
CTH
VCC
VE
SP
VO
GND
SP
J17
R139
1K00
1
2
3
7
4
SP
6
5
5
6
7
8
9
SP
10
ISOLATION BARRIER
SCHEMATIC
GND
R184
1K00
100nF 25V
8
+5V DIGITAL
14
C120
U26
HCPL-2601
GND
13
SP
DTA143XKA
TO J2 ON NELLCOR MP506
+5 ANALOG
12
D_FROM_SPO2
D_TO_SPO2
GND
3
U25
HCPL-2601
NELLCOR
C-LOCK
2
PWA, MAIN BOARD, PROCARE
MASIMO
+5V
GND
GND
TO J3 ON MASIMO MS-5
GND
RESET
RECEIVE (MS-5 IN)
TRANSMIT (MS-5 OUT)
SP
Schematic - Main Board
P/N 2008855 Rev B
(9 of 10) page 5-21/22
P5TEMP
P5TEMP
R166
1K00
U36
TL431
C137
R186
10K0
1
8
T
C130
10U0
2 3 6 7
16V
R172
Temperature
Probe Connector
13K7
0.1%
P5TEMP
R193
10K0
3
L14
J14
2
3
5
R167
100R
3
DIN 20
DOUT 21
SCLK 22
AD0
AD1
AD2
AD3
3
4
X_IN
X_OUT
5
RESET-0
DSYNC-0
POL
BUFEN
PDWN-0
6
5
4
3
DRDY_FROM_T_ADC
2
1
P5TEMP
ADS1240
Temp PGM Connector
6
T
DO NOT POPULATE
J15
R156
6
18
24
7
10K0
R155
10K0
DGND1 2
DGND2 8
ISOLATION BARRIER
T
T
C136
100NF
25V
D23
D_TO_T_ADC
D_FROM_T_ADC
SCLK_TO_T_ADC
V_THERM
1K00
C152
BAS16
1
11
12
13
14
16 AGND
R157
BLM11B221SB
4
CLK_TADC
BAS16
BLM11B221SB
L9
1
DVDD 1
9 REF+
10 REF-
D24
1
17 AVDD
DRDY-0 23
15 AINCOM
U34 CS-0 19
T
P5TEMP
P5TEMP
100nF 25V
100NF
25V
T
P5TEMP
C138
T
T
P5TEMP
P5TEMP
L7
1
1
R168
R197 R164
30R 499K
R194 R195 R196
30R 30R 30R
D28
BAS16
T
Q21
SI2307DS
2
1
R192
10K0
3
3
R171
1K00
19
20
1
2
3
D29
BAS16
1
R160
MON_HTR
10K0
18
C134
T
100NF
25V
P5TEMP
17
1
D22
22P0
BAS16
C131
BLM11B221SB
XL4
4.0MHZ
14
13
12
11
10
9
RB7
RB6
RB5
RB4/PGM
RA0/AN0
RB3
RB2/TX
RA1/AN1
8
RA2/AN2/VREF RB1/RX
7
RA3/AN3/CMP1 RB0/INT
RA4/T0CKI/CMP2
OSC1
U35
PIC16F628
OSC2/OUT
C132
T
3
15
VDD1
16
VDD2
4
MCLR-0
R162
0R0
VSS1
5
VSS2
6
T
T
R191
2K21
R154
10K0
U33
4N35
T
100nF 25V
BLM11B221SB
L10
100nF 25V
P5TEMP
C133
T
3
P3V3
2
2K0
AN
C
B
CTH
E
D_FROM_TEMP
5
6
4
Q23
D_TO_TEMP
DTA143XKA
Logic
R198
10K0
R188
100K
5
6
4
T
T
R169
1K00
U32
4N35
T
C
AN
B
E
CTH
1
2
R187
10K0
T
22P0
3
D25
TEMP_PROBE_IN
Q22
BAS16
1
T
SI2306DS
3
1
2
R158
10K0
T
P3V3
C142
2U2
V_JUMPER
C135
100NF
25V
R165
499K
R132
10K0
R189
EN_HTR
499K
Temp Probe Switch Connector
P5D
J13
1
2
3
16V
T
T
T
SCHEMATIC
PWA, MAIN BOARD, PROCARE
Schematic - Main Board
P/N 2008855 Rev B
(10 of 10) page 5-23/24
P5D
C3
P5D
PDG_L[0:12]
1
23
Y10
Y11
EL
Y12
E
Y13
D1
P5D
HCT132
Q1
DTC143ZKA
L
L
Q3
DTC143ZKA
R42
180R
PDG_L12
100NF
50V
DG12
SA0
2
SA1
15
SA2
13
SA3
11
A
SA4
HCT132
C
14
P5D
U1
HCT132
P5D
U1
GND
S1
R23
S2
330
SA1
330
R24
SA2
S3
R25
330
SA3
S4
330
R26
SA4
S5
R27
330
SA5
330
R28
SA6
S6
C4
SA0
2
SA1
15
SA2
13
SA3
11
8
2
IO1
CLK
IO2
Q0
IO3
OE1
3
19
DS0
1
19
HCT299
U4
IO4
OE2
IO5
S0
IO6
S1
IO7
Q7
P5D
CLR
9
DS7
GND
9
PS0
13
PS1
6
PS2
14
PS3
5
PS4
15
PS5
4
PS6
16
PS7
C5
100NF
VCC
11
12
8
IO0
DS0
IO1
CLK
IO2
Q0
IO3
HCT299
2
OE1
U3
3
OE2
1
S0
19
19
S1
IO4
IO5
IO6
IO7
Q7
P5D
CLR
9
9
GND
DS7
7
PS8
13
PS9
6
PS10
14
PS11
5
PS12
15
PS13
4
PS14
16
PS15
330
16
S10
330
R35
13
S11
R30
330
3
S12
330
R34
5
S13
R31
330
11
S14
330
R33
15
S15
R32
330
330
DG7
7
DP
1
DIG1
2
DIG2
6
DIG3
8
DIG4
DG10
15
Q9
DTC143ZKA
L
SA2
13
SA3
11
g
D2
E1
e
9
5
c
E2
SA4
d
F
DP
G
7
SA5
3
SA6
14
10
DP
4
COM
12
12
COM
17
17
COM
LED29
LTC2621JD
A
a
B
C
D1
f
b
g
D2
E1
S8
e
E2
c
d
F
DP
7
SA5
3
SA6
14
C
DIASTOLIC
LED18
DMR20A-1 RED
a
C
f
D1
b
SA0
2
SA1
15
SA2
13
SA3
11
g
D2
L
Q10
DTC143ZKA
L
DG9
R50
180R
DG8
R51
180R
Q11
DTC143ZKA
Q12
DTC143ZKA
L
L
Q14
DTC143ZKA
620
12
620
R103
6
S11
R99
620
1
S12
620
R102
4
S13
R100
620
S14
620
R101
G
DP
COM
COM
COM
F
S0
a
B/L2
a
f
D
b
L1
g
E
F
e
7
G
3
DP
DG0 2
DIG1
DG1 5
DIG2
DG2 138
DIG3
L1,L2,L3
f
b
b
g
g
e
c
e
c
L2
d
f
c
d
DP
12
R105
200
11
200
R110
3
S3
R106
200
4
S4
200
R109
2
S5
R107
200
15
S6
200
R108
d
DP
R111
S2
S1
a
L3
C/L3
16
LED28
LTC4624Y
RED
200
DP
YELLOW
A/L1
a
B/L2
C/L3
D
f
a
b
F
e
8
G
6
DP
DG6 1
DG1
DG7 5 DG2
DG8 7
DIG3
14
L1,L2,L3
f
L1
g
E
E1
e
E2
d
F
C
DP
G
SA4
7
SA5
3
SA6
14
SA1
15
SA2
13
SA3
11
9
5
c
d
F
DP
G
SA4
7
SA5
3
SA6
14
10
DP
4
COM
12
COM
17
COM
e
E2
12
COM
2
g
E1
4
COM
b
D2
10
DP
f
D1
5
c
a
B
SA0
17
COM
LED27
LTC4624JD
A
C
D1
f
b
g
D2
E1
R97
12
S1
R37
330
11
S2
330
R96
3
S3
R57
330
4
S4
330
R95
2
S5
R58
330
15
S6
330
R94
8
S0
a
B
e
E2
c
d
F
b
f
e
e
c
a
b
L3
f
g
e
d
DP
b
g
c
L2
d
c
d
DP
DP
330
DG9
DP
G
1
5
DG10
DP
DG11
COM
7
14
COM
6
C/L3
a
D
f
a
b
f
b
g
g
e
d
DP
19
3
18
4
b
g
E
F
e
f
L1
17
5
16
6
15
R120
7
14
200
8
13
R122
9
12
200
10
11
R124
a
L3
b
f
g
e
c
b
g
e
c
c
L2
G
d
DP
DG1
d
DP
d
DP
DP
DG2
DIG3
L1,L2,L3
COM
a
f
c
d
20
R119
200
200
R121
200
R123
200
S15
S14
S13
S12
S11
S15
S[0:15]
AUTO/TIME
b
e
a
RED
2
A/L1
B/L2
GURX10D
1
RED
LED11
LTC2623JD
g
c
LED9
SPO2
R118
13
R112
620
15
S10
620
R117
2
S11
R113
620
6
S12
620
R116
5
S13
R114
620
16
S14
620
R115
S8
g
E
G
R98
S10
PULSE
A/L1
LED19
DMR20A-1 RED
A
9
a
f
D
15
620
RED
a
B
R104
S9
S9
R29
DG9
b
2
SA1
A
S9
DG8
f
D1
SA0
TEMP
LED30
LTC4627JD
20
P5D
SA4
17
14
C
4
B
17
R36
a
B
10
A
12
S8
14
COM
4
18
3
SA6
COM
10
10
P5D
R46
180R
MAP
DG4
12
Q8
DTC143ZKA
L
LED16
DMR20A-1 RED
A
7
SA5
COM
DG3
11
7
11
DP
5
20
IO0
13
SA3
SA4
DP
G
9
100NF
VCC
SA2
LED17
DMR20A-1 RED
P5D
needs pull up on main board
P5D
Q7
DTC143ZKA
L
R47
180R
Q26
2SB1188
SA[0:6]
330
R56
100R
Q6
DTC143ZKA
LED10
DMR20A-1 RED
DG1
U1
SA0
15
5
c
d
F
17
S0
GND
e
E2
12
R14
2
SA1
9
DG0
100R
E1
4
HCT132P5D
R55
100R
GND
b
SA0
g
D2
10
100NF
1
J1
3
SA6
f
D1
7
SA5
a
B
9
P5D
C9
SYSTOLIC
LED13
DMR20A-1 RED
Q13
DTC143ZKA
L
P5D
R131
L
R48
180R
R2
10K0
1%
Q2
2SB1188
V_IN
10
PBAT
9
SPI_CLK
8
SPI_MOSI
7
SW_PWR
6
CS_DISPLAY
5
P5D
4
SW_MUX
3
GND
2
Q5
DTC143ZKA
L
R49
180R
R12
10K0
1%
Q25
2SB1188
DG[0:12]
5
PBAT
Q4
DTC143ZKA
L
R44
180R
12
C1
CONN_S_2X5_HDRF
R45
180R
R11
10K0
1%
Q24
2SB1188
15
R39
200R
R40
470K
R43
180R
R10
10K0
1%
Q23
2SB1188
DG7
PDG_L12
R52
180R
R9
10K0
1%
Q22
2SB1188
DG6
PDG_L11
14
GND
U1
BAT54C
PDG_L10
19
R53
180R
R8
10K0
1%
Q21
2SB1188
16
Y15
GND
20
R41
180R
R7
10K0
1%
Q20
2SB1188
13
Y14
P5D
R61
10K0
1%
PDG_L9
R6
10K0
1%
Q19
2SB1188
PDG_L9
HEF4514
U2
PDG_L8
17
R5
10K0
1%
Q18
2SB1188
PDG_L8
18
18
R3
10K0
1%
Q17
2SB1188
PDG_L7
R60
10K0
1%
17
10
9
Y9
PDG_L7
R4
10K0
1%
Q16
2SB1188
PDG_L6
Y8
16
PDG_L6
4
R13
10K0
1%
Q15
2SB1188
DG5
P5D
4
5
R1
10K0
1%
DG6
DS7
GND
Y7
PDG_L5
DG11
9
Y6
15
PDG_L4
PDG_L5
Q7
CLR
Y5
6
DG4
IO7
A3
PDG_L3
7
PDG_L4
IO6
S1
Y4
DG3
S0
5
A2
PDG_L2
8
PDG_L3
IO5
22
Y3
PDG_L1
10
DG2
IO4
21
DIG_MUX3
A1
9
PDG_L2
HCT299
U5
OE2
DIG_MUX2
14
Y2
DG5
IO3
6
Y1
A0
DG1
Q0
3
PDG_L1
1
19
P5D
IO2
OE1
3
19
CLK
2
DIG_MUX1
PDG_L0
2
P5D
IO1
DIG_MUX0
13
DG10
12
8
DS0
7
PDG_L10
100R
IO0
PDG_L0
DG11
20
VCC
11
11
PDG_L11
Y0
DG2
24
VCC
DG0
C2
100NF
R127
PBAT
100NF
e
c
c
d
620
d
DP
DP
DG3
DP
DG4
DG5
DG6
DG11
RED
A/L1
a
B/L2
C/L3
D
f
E
F
e
7
G
3
DP
1
DIG1
14
DIG2
11
DIG3
8
DIG4
12
L1,L2,L3
a
b
f
g
a
b
L1
f
g
c
d
e
f
g
c
d
DP
a
L3
b
e
c
L2
d
DP
b
g
e
c
d
DP
DP
17
18
10
PS[0:15]
Q36
DTD123EK
L
SCHEMATIC
L
Q38
DTD123EK
L
Q39
DTD123EK
L
Q40
DTD123EK
L
S15
S14
S13
S12
S11
Q37
DTD123EK
Q41
DTD123EK
L
Q42
DTD123EK
PS15
L
PS14
Q35
DTD123EK
PS13
L
S10
S9
S8
Q34
DTD123EK
S[0:15]
PS12
L
PS11
Q33
DTD123EK
PS10
L
S7
S6
Q32
DTD123EK
PS9
L
PS8
Q31
DTD123EK
PS7
L
S5
S4
Q30
DTD123EK
PS6
L
PS5
Q29
DTD123EK
PS4
L
S3
S2
Q28
DTD123EK
PS3
Q27
DTD123EK
PS1
PS0
L
L
PS2
S0
S1
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
PROCARE USER INTERFACE BOARD
Schematic User Interface Board
P/N 2008741 Rev B
(1 of 2) page 5-25/26
PCB BOARD SWITCH LOCATIONS
PBAT
C12
C11
C10
100NF
100NF
100NF
50V
50V
50V
C8
C6
C7
16V
16V
16V
47U0
SILENCE
2
5
INFLATE
ALARM
1
3
CYCLE
7
0
HISTORY
6
8
PRINT
4
9
ON/OFF
P5D
47U0
+
-
47U0
MENU
V_IN
DG[0:12]
DG3
LED37
APTD3216QYC
GREEN
PDG_L[0:11]
DG4
CHARGING
R126
10K0
1%
LED21
APTD3216QYC
GREEN
DG5
R135
10K0
1%
SW9
SW_PWR
A
B
LED66
APTD3216QYC
GREEN
ON/OFF
CHARGING
degF
Q43
DTD123EK
L
D2
BAT54C
LED61
AP3216SURC
RED
R20
38R3
R18
38R3
S7
SW0
A
LED62
AP3216SURC
RED
degC
LED65
APTD3216QYC
GREEN
SW_MUX
B
HISTORY
BATT
LOW
RIGHT
BATT
LOW
LEFT
LED56
APTD3216SYCK
YELLOW
LED54
AP3216SURC
RED
BELL
LED69
APTD3216SYCK
YELLOW
LED60
APTD3216SYCK
YELLOW
R133
38R3
R75
22R
S7
S15
R136
10K0
1%
LED68
APTD3216QYC
GREEN
R77
22R
R134
38R3
S15
S7
BATTERY
MIDDLE
BATTERY
RIGHT
LED55
AP3216SURC
RED
S15
2
1
LED15
APTD3216QYC
GREEN
BATTERY
LEFT
LED1
APTD3216QYC
GREEN
LED57
APTD3216QYC
GREEN
LED5
APTD3216QYC
GREEN
R16
22R
R74
22R
S15
S7
PDG_L0
SW1
A
B
ALARM
PDG_L1
DG12
SW2
D6
A
B
SILENCE
BAT54C
B
PULSE
LOW
minus
R125
10K0
1%
SW3
A
LED67
AP3216SURC
RED
PDG_L2
R64
38R3
PDG_L3
CYCLE
SW4
A
D5
BAT54C
B
S8
PDG_L4
MENU
LED53
AP3216SURC
RED
PULSE
HIGH
LED40
AP3216SURC
RED
LED52
AP3216SURC
RED
SpO2
LOW
SpO2
HIGH
LED50
AP3216SURC
RED
DIA
LOW
LED49
AP3216SURC
RED
DIA
HIGH
LED46
AP3216SURC
RED
LED44
AP3216SURC
RED
SYS
LOW
LED42
AP3216SURC
RED
SYS
HIGH
LED38
AP3216SURC
RED
LED39
AP3216SURC
RED
LED41
AP3216SURC
RED
LED51
AP3216SURC
RED
LED48
AP3216SURC
RED
LED47
AP3216SURC
RED
LED45
AP3216SURC
RED
LED43
AP3216SURC
RED
R79
22R
R65
22R
R63
22R
R38
22R
R21
22R
R19
22R
R17
22R
R15
22R
S6
S7
S5
S4
S3
S2
S1
S0
SW5
A
B
PDG_L5
INFLATE
DG0
DG1
SW6
D4
A
SW7
A
DG12
PDG_L6
MINUS
BAT54C
DG2
B
B
PDG_L7
AL VOL
RIGHT
LED2
APTD3216QYC
GREEN
AL VOL
LEFT
LED58
APTD3216QYC
GREEN
LED8
APTD3216QYC
GREEN
LED6
APTD3216QYC
GREEN
LED59
APTD3216QYC
GREEN
R70
22R
R72
22R
R22
22R
LED3
APTD3216QYC
GREEN
AL VOL
MIDDLE
PUL VOL
LEFT
LED64
APTD3216QYC
GREEN
PUL VOL
MIDDLE
LED7
APTD3216QYC
GREEN
PLUS
SW8
A
D3
BAT54C
LED63
APTD3216QYC
GREEN
B
PRINT
PUL VOL
RIGHT
LED35
APTD3216QYC
GREEN
LED22
APTD3216QYC
GREEN
LED34
APTD3216QYC
GREEN
AUTO
RIGHT
HISTORY
LED20
APTD3216QYC
GREEN
LED4
APTD3216QYC
GREEN
R68
22R
R80
22R
LED32
APTD3216QYC
GREEN
AUTO
LEFT
LED26
APTD3216QYC
GREEN
INF PRES
RIGHT
LED36
APTD3216QYC
GREEN
LED70
APTD3216QYC
GREEN
LED14
APTD3216QYC
GREEN
LED33
APTD3216QYC
GREEN
R90
22R
R137
38R3
R89
22R
R87
22R
2
INF PRES
MIDDLE
LED31
APTD3216QYC
GREEN
1
LED25
APTD3216QYC
GREEN
LED24
APTD3216QYC
GREEN
INF PRES
LEFT
LED12
APTD3216QYC
GREEN
LED23
APTD3216QYC
GREEN
PDG_L8
S7
S15
S15
R62
22R
S7
S7
S15
S15
S14
PROCARE USER INTERFACE BOARD
S14
S13
R85
22R
S12
R84
22R
S11
R82
22R
S10
Schematic User Interface Board
P/N 2008741 Rev B
(2 of 2) page 5-27/28
0086
2009381-001 B
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