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GE Healthcare
DINAMAP
Service Manual
ProCare Monitor
DINAMAP ProCare Monitor
English
2009381-001 C (paper)
© 2007 General Electric Company.
All Rights Reserved.

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Summary of Contents for GE DINAMAP ProCare

  • Page 1 GE Healthcare DINAMAP ProCare Monitor ™ Service Manual DINAMAP ProCare Monitor English 2009381-001 C (paper) © 2007 General Electric Company. All Rights Reserved.
  • Page 3 GE Healthcare DINAMAP ProCare Monitor ™ Service Manual DINAMAP® ProCare Monitor Service Manual English 2009381-001 C (paper) © 2007 General Electric Company. All Rights Reserved.
  • Page 4 Technologies. GE is a registered trademark of General Electric Company. All other product and brand names are trademarks or registered trademarks of their respective companies. ©2005, 2006 GE Medical Systems Information Technologies. All rights reserved. No part of this manual may be reproduced without the permission of GE Medical Systems Information Technologies.
  • Page 5: Table Of Contents

    Introduction ....... . . 1-1 Revision History ..........1-3 Manual Purpose .
  • Page 6 Basic Components ..........2-4 Front Panel Controls and Indicators .
  • Page 7 Procedures ..........3-7 Inflation Pressure Default Setting .
  • Page 8 Parameter Test Procedures ........4-10 Setup ........... 4-10 Leakage Testing .
  • Page 9 Technical Specifications ..... . A-1 Specifications ........... A-3 Mechanical .
  • Page 10 Appropriate Use of NIBP Simulators ... . B-1 Appropriate Use of NIBP Simulators ....... B-3 NIBP Accuracy .
  • Page 11: Introduction

    Introduction ® Revision C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 12 For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 13: Revision History

    Ordering Manuals A paper copy of this manual will be provided upon request. Contact your local GE representative and request the part number on the first page of the manual. Safety Information The information presented in this section is important for the safety of both the patient and operator.
  • Page 14: Responsibility Of The Manufacturer

    Introduction: Safety Information Responsibility of the Manufacturer GE is responsible for the effects on safety, reliability, and performance only if: assembly operations, extensions, readjustments, modifications, or repairs are carried out by persons authorized by GE; the electrical installation of the relevant room complies with the requirements of appropriate regulations;...
  • Page 15: Warnings, Cautions, And Notes

    WARNING: These Monitors should not be used on patients who are connected to cardiopulmonary bypass machines. If powering the Monitor from an external power adapter or converter, use only GE Medical Systems Information Technologies-approved power adapters and converters. The Monitor does not include any user-replaceable fuses. Refer servicing to qualified service personnel.
  • Page 16: Cautions

    Introduction: Equipment Symbols Cautions Do not use replacement batteries other than the type supplied with the Monitor. Replacement batteries are available from GE Medical Systems - Accessories and Supplies. The ProCare Monitor is designed to conform to Electromagnetic Compatibility (EMC) standard IEC 601-1-2, 1993 and will operate accurately in conjunction with other medical equipment which also meets this requirement.
  • Page 17 Introduction: Equipment Symbols Inflate/Stop Cycle History Print On/Off Battery Power External Communications Port Connector Charging Defibrillator-proof type BF equipment External AC or DC power indicator Class II equipment according to IEC 60536 Packaging label depicting the transportation and storage atmospheric pressure range of 500 to 1060 hPa. WASTE OF ELECTRICAL AND ELECTRONIC EQUIPMENT (WEEE): This symbol indicates that the waste of electrical and electronic equipment must not be...
  • Page 18: Service Requirements

    Any unauthorized attempt to repair equipment under warranty voids that warranty. It is the user’s responsibility to report the need for service to GE Medical Systems Information Technologies or to one of GE’s authorized agents. Failure on the part of the responsible individual, hospital or institution using this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards.
  • Page 19: Intended Use

    If you are unable to resolve the problem after checking these items, contact GE Medical Systems Information Technologies. Prior to calling, please be prepared to provide:...
  • Page 20: Service

    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. Contact GE Medical Systems Information Technologies at 1-800-558-7044.
  • Page 21: Repair Parts

    All loaners provided to customers must be returned within the specified time stated on the loaner agreement or a rental fee will be incurred. Repair Parts Repair parts can be ordered from GE Medical Systems Information Technologies: Via phone: 1-800-558-7044, or Via FAX: 1-800-421-6841 Exchange replacement assemblies such as Circuit Board Assemblies also are available;...
  • Page 22: Packaging Material

    At the end of its service life, the product described in this manual, as well as its accessories, must be disposed of in compliance with the guidelines regulating the disposal of such products. If you have questions concerning disposal of the product, please contact GE Medical Systems Information Technologies or its representatives. ®...
  • Page 23: Equipment Overview

    Equipment Overview ® Revision C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 24 For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 25: Equipment Description

    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 GE Medical Systems Information Technologies Customer Service immediately.
  • Page 26: Basic Components

    Equipment Overview: Basic Components Basic Components Front Panel Controls and Indicators Buttons 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.
  • Page 27: Front Panel

    Equipment Overview: Basic Components 10. Temperature probe cover storage: Box of probe covers is stored here. 11. History button: Press to activate the History mode to view stored patient data. The most recent entries are displayed first. Press and hold the button for 2 seconds to clear all entries stored.
  • Page 28 Equipment Overview: Basic Components 20. Inflate pressure: lights to indicate you are making a change to the inflation pressure. 21. Pulse Rate window: 3-digit yellow LED shows pulse rate in beats per minute. 22. SpO pulse indicator: Red LED bar flashes to indicate that real-time pulse rate measurements are being derived from SpO signals.
  • Page 29: Product Compliance

    Defibrillation protected. When used with the recommended accessories, the Monitor is protected against the effects of defibrillator discharge. If monitoring is disrupted by the defibrillation, the Monitor will recover. DINAMAP PROCARE MONITOR CLASSIFIED WITH RESPECT TO ELECTRIC SHOCK, FIRE AND MECHANCIAL AND OTHER SPECIFIED HAZARDS ONLY IN ACCORDANCE WITH CAN/CSA C22.2 NO.
  • Page 30: Theory Of Operation

    Equipment Overview: Theory of Operation Theory of Operation 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...
  • Page 31: Spo2 (Model 300 And 400)

    Equipment Overview: Overall Principles of Operation (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 both 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.
  • Page 32 Equipment Overview: Overall Principles of Operation Monitor is unable to find any pulse within several seconds, it will deflate to the next step. The process of finding two matched pulses at each step provides artifact rejection due to patient movement and greatly enhances the accuracy of the Monitor.
  • Page 33: Systolic Search

    Equipment Overview: Overall Principles of Operation Systolic Search If systolic pressure is not found, the NIBP parameter can search at cuff pressures higher than the initial target pressure. The parameter will inflate the cuff above the initial target pressure to get more data in the systolic region. The maximum pressure allowed in systolic search is limited by the normal range for cuff pressures.
  • Page 34: Temperature (Model 200 And 400)

    Equipment Overview: Functional Description 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.
  • Page 35: User Interface (Ui) Board Pwa

    Equipment Overview: Functional Description 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.
  • Page 36: Printer

    Equipment Overview: Functional Description 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 the primary processor, the following will occur: PR_CLK signal - transfer the data into print head PR_DI signal - serial dot to be printed...
  • Page 37 Equipment Overview: Functional Description ® Revision C DINAMAP ProCare Monitor Service Manual 2-15 2009381-001...
  • Page 38 Equipment Overview: Functional Description ® 2-16 DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 39: Installation

    Installation ® Revision C DINAMAP ProCare Patient Monitor Service Manual 2009381-001...
  • Page 40 For your notes ® DINAMAP ProCare Patient Monitor Service Manual Revision C 2009381-001...
  • Page 41: Connections

    IEC 601-1, configured to comply with IEC 601-1-1. Right-Side Panel External DC power socket: To be used with approved GE Medical Systems Information Technologies AC-DC power converter ONLY. ® Revision C...
  • Page 42: Powering The Monitor

    Installation: Connections Powering the Monitor Power Sources The ProCare Monitor is designed to operate from an internal lead-acid battery. NOTE:The ProCare Monitor is not designed to operate without an internal battery. Battery Charging The Monitor charges the Lead-Acid battery whenever the AC power supply is in use.
  • Page 43: Unpacking And Preparation For Installation

    Installation: Unpacking and Preparation for Installation Battery charging will take place as long as the Monitor remains connected to an external AC power source. NOTE:: To prolong the life of the battery, keep the Monitor connected to a DC power supply whenever possible.
  • Page 44: Configuring Your Procare Monitor

    Installation: Configuring Your ProCare Monitor Configuring Your ProCare Monitor Operating Modes The ProCare Monitor can operate in one of four modes: clinical, configuration, advanced configuration, and service. Clinical Mode Clinical mode is the Monitor’s normal operating mode. While this mode is active, alarm limits and a few other commonly used settings are adjustable.
  • Page 45: Setting The Date And Time

    Installation: Configuring Your ProCare Monitor Pressing the Menu button cycles through all the configuration option pages. After all options pages have been displayed, the display returns to the 1 configuration mode page (displaying CFG). You can use the + and - buttons to make changes to settings.
  • Page 46: Inflation Pressure Default Setting

    Installation: Configuring Your ProCare Monitor Inflation Pressure Default Setting – Procedures Enter the configuration mode: with the Monitor off, press and hold the Menu button at the same time as pressing and holding the On/Off button for 3 seconds, or press Menu until the Inflate Pressure is lit on the display and the pressure is displayed in the Diastolic window.
  • Page 47: Procedure For Units With Masimo® Technology

    Installation: Configuring Your ProCare Monitor Procedure for units with Masimo® Technology (Refer to the Masimo® section for options) Enter the configuration mode: with the Monitor off, press and hold the Menu button at the same time as pressing and holding the On/Off button for 3 seconds.
  • Page 48 Installation: Configuring Your ProCare Monitor The advanced configuration mode option pages are as follows: Displayed on Monitor Function Advanced Configuration Mode announcement (No settings are entered on this page.) Remote mode 0 : Remote mode is disabled 1 : Remote mode is enabled Host Comm unit address 32 : This is the default value.
  • Page 49: Service Mode

    Installation: Configuring Your ProCare Monitor Service Mode Service mode is entered by holding the Cycle button while powering on with the On/Off button. You can press the Cycle button to advance through the available service mode pages. NOTES Only transducer calibration pages are available until calibration is valid. Calibration and other service mode setting changes will not be retained unless the “Save Settings”...
  • Page 50 Installation: Configuring Your ProCare Monitor Displayed on Monitor Function 6 (in “min” window) Language The number displayed in Pulse Rate display window indicates the language setting. These range from 0 to In “MAP/Cuff” window: 20. For example, 0 indicates English. The language setting is used in printed reports.
  • Page 51: Host Communications Connector

    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.
  • Page 52 Installation: Host Communications Connector Pin # 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 ®...
  • Page 53: Maintenance

    Maintenance ® Revision C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 54 For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 55: Preventative Maintenance

    Maintenance: Preventative Maintenance Preventative Maintenance WARNING Failure on the part of all responsible individuals, hospitals or institutions, employing the use of this device, to implement the recommended maintenance schedule may cause equipment failure and possible health hazards. The manufacturer does not, in any manner, assume the responsibility for performing the recommended maintenance schedule, unless an Equipment Maintenance Agreement exists.
  • Page 56: Cleaning

    Maintenance: Cleaning Cleaning Cleaning the Monitor CAUTIONS Never pour or spray water or any cleaning solution on the equipment or permit fluids to run behind switches, into connectors, into the recorder, into the temperature probe well, or into any ventilation openings in the equipment. Do not let fluid “pool”...
  • Page 57: Display

    Maintenance: Cleaning Any type of solution that contains ammonium chloride, conductive solutions, wax or wax compounds Sodium salts NOTE:Never autoclave or steam clean the monitor, cuffs, or accessories. Display To clean the display screen, use a soft, clean cloth dampened with a glass cleaner.
  • Page 58: Temperature Devices

    Allow 2 hours for drying. The user has the responsibility to validate any deviations from the recommended method of cleaning and disinfection. For additional information on infection control procedures, contact GE Medical Systems Information Technologies Technical Support. Temperature Devices Do not immerse predictive temperature probes. The probe may be cleaned with a solution of 10% bleach in water.
  • Page 59: Battery Care

    Monitor with the battery in a discharged condition. When the battery will no longer hold a charge, remove and replace it. Failure to replace the battery with the same GE Medical Systems Information Technologies part number may result in shorter battery life. Battery charging will take place as long as the Monitor remains connected to an external DC power source.
  • Page 60: Replacing The Battery

    Maintenance: Long-Term Storage Replacing the Battery Unplug the Monitor from the DC power source. Looking at the bottom of the ProCare Monitor, remove the battery compartment cover by removing the four screws that secure the cover and help card tray. Remove the help card tray and battery door cover.
  • Page 61: Fuses

    Maintenance: Parameter Level Functional Testing Replacement batteries can be obtained from GE Medical Systems Information Technologies. NOTE:: The replacement part number of the battery is 633178CR. Use of nonspecified batteries can cause internal damage to the Monitor or cause patient/user safety issues.
  • Page 62: Calibration Procedures And Tests

    Digital manometer (with range to 350 mmHg) Stopwatch/timer (capable of measuring seconds) Adult BP cuff, Neonate BP cuff, hose, inflation bulb, and associated tubing Calibration kit (p/n 320246, available through GE Medical Systems cable (for appropriate SpO type, if SpO...
  • Page 63: Leakage Testing

    Maintenance: Parameter Level Functional Testing Consult the following diagram for pneumatic setup guidelines. MANDREL 2 TUBE BP CUFF Leakage Testing NOTE:To enter Service Mode press and hold the Cycle button while pressing the On/Off button. Turn unit on and enter Service Mode. Press Cycle button and 1 should appear in the min window.
  • Page 64: Pressure Transducer Verification

    Maintenance: Parameter Level Functional Testing Pressure Transducer Verification NOTE:To enter Service Mode press and hold the Cycle button while pressing the On/Off button. Turn unit on and enter Service Mode. The min window should display 0. Open the valve on the inflation bulb and remove all pressure from the system (manometer reads zero).
  • Page 65: Overpressure Verification

    Maintenance: Parameter Level Functional Testing Close valve on bulb and slowly inflate pressure to 200 mmHg (using the manometer as reference). Press Menu button when pressure reads exactly 200 mmHg to save calibration setting. Press Cycle button until 6 appears in the min window. Press and hold Menu button until monitor beeps, which acknowledges that data was saved.
  • Page 66: External Dc Verification

    Maintenance: Parameter Level Functional Testing External DC Verification Plug the power brick into the Monitor. Verify that the CHARGING indicator is illuminated. BP Determination NOTE:For best results, it is important to be seated and not moving, talking, eating, and/or smoking, etc. while taking your blood pressure. If you are uncertain as to the proper technique, consult the operation manual.
  • Page 67 Maintenance: Parameter Level Functional Testing Alaris Turbo Temp Probe Date Code Turn Monitor off. Make sure the temp probe is properly stored in the probe well. Disconnect the temp probe cable from the monitor. Connect Temp simulator; set to 80.2°F. Turn the Monitor on.
  • Page 68: Printer Output Test

    Maintenance: Parameter Level Functional Testing (Perform only if equipped with SpO module) Connect the appropriate SpO probe and cable to the SpO connector. Place the probe on your finger. Verify the unit displays a: Pulse value Saturation value Signal Strength Bar Graph Remove the sensor from your finger to generate an E23 alarm and to sound the speaker.
  • Page 69: Test Results Form

    Maintenance: Test Results Form Test Results Form Description Actual Pass-Fail-N/A LEAKAGE Leakage Result (mmHg) PRESSURE TRANSDUCER VERIFICATION Pressure reading at 200mmHg, top display - Systolic Pressure reading at 200mmHg, bottom display - Diastolic Pressure reading at 150mmHg, top display - Systolic Pressure reading at 150mmHg, bottom display - Diastolic Pressure reading at 100mmHg, top display - Systolic...
  • Page 70 Maintenance: Test Results Form Description Actual Pass-Fail-N/A Heart rate reading (bpm) Systolic reading (mmHg) Diastolic reading (mmHg) MAP reading (mmHg) Heart rate reading (bpm) BP OVERPRESSURE "E80" displayed on SYSTOLIC display Pump will not start Overpressure alarm can be cleared TEMPERATURE TEST Temperature reading at 80.2°...
  • Page 71: Troubleshooting

    Troubleshooting ® Revision C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 72 For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 73: Alarm Code Interpretation

    Troubleshooting: Alarm Code Interpretation 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.
  • Page 74 Troubleshooting: Alarm Code Interpretation The SPO2 window shows the Time the error occurred. The Pulse Rate window shows the error code that occurred at the recorded time. 10. To print the error log, press the Print button while viewing the log. Error Code Can be Source...
  • Page 75 Troubleshooting: Alarm Code Interpretation Error Code Can be Source Definition Probable Source or Problem Silenced? Battery Battery too low to operate the unit Charge battery External DC source failed Replace battery SPO2 Failed SPO2 sensor Replace SPO2 sensor SPO2 SPO2 Sensor off finger Reposition SPO2 sensor SPO2 SPO2 No signal...
  • Page 76 Troubleshooting: Alarm Code Interpretation ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 77: Parts List, Drawings, And Replacement

    Parts List, Drawings, and Replacement ® Revision C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 78 For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 79: Ordering Parts

    This section of the manual provides parts lists for the ProCare Monitor. Parts lists should be used in conjunction with the other chapters of this manual. GE makes every effort possible to provide the most up-to-date reference documentation for your equipment. However, in special cases involving field- installed upgrades, the revision level of a diagram or parts list in this manual may not reflect the revision level of your unit’s subassemblies.
  • Page 80 Parts List, Drawings, and Replacement: Service Parts Part Part Number Air Hose 12-ft Adult/Pediatric, Screw Connector 107365 Air Hose 24-ft Adult/Pediatric, Screw Connector 107366 Air Hose 12 ft Neonatal 107368 2458 ® SENSA-CUF 2-Tube Screw Connector, Infant 2460 ® SENSA-CUF 2-Tube Screw Connector, Child 2462 ®...
  • Page 81 Parts List, Drawings, and Replacement: Service Parts Part Part Number NELLCOR**: Pulse Oximeter Cable DOC-10 2008773-001 DuraSensor Adult Oxygen Sensor DS100A Masimo***: Adult Reusable Sensor, LNOP NR-195 2008278-001 Pulse Oximeter Cable (PC08) 2009743-001 *IVAC is a trademark of Alaris Medical Systems. **NELLCOR is a trademark of Nellcor Puritan Bennett.
  • Page 82: Field-Replaceable Units (Frus)

    Parts List, Drawings, and Replacement: Service Parts Field-Replaceable Units (FRUs) WARNING REPAIR TO THE FRU LEVEL - Field repairs are recommended to the field replaceable unit (FRU) only. Attempting a field repair on a PCB or a factory sealed component or assembly could jeopardize the safe and effective operation of the monitor.
  • Page 83 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2010478-001 KIT, FRU, LABEL, ENGLISH, DPC300, PRINT 2010479-001 KIT, FRU, LABEL, ENGLISH, DPC200, PRINT 2010480-001 KIT, FRU, LABEL, ENGLISH, DPC100, PRINT 2011645-001 FRU PROCARE ENGLISH KEYPAD LABEL SET, 100-400 2008329-001 PLASTIC DISPLAY COVER 400 ENGLISH 2010371-001 PLASTIC DISPLAY COVER, DPC200, NORWEGIAN...
  • Page 84 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2008510-001 PLASTIC DISPLAY COVER 400 ITALIAN 2010401-001 PLASTIC DISPLAY COVER, DPC200, HUNGARIAN 2008511-001 PLASTIC DISPLAY COVER 300 ITALIAN 2010402-001 PLASTIC DISPLAY COVER, DPC100, HUNGARIAN 2008512-001 PLASTIC DISPLAY COVER 200 ITALIAN 2010403-001 PLASTIC DISPLAY COVER, DPC400, CZECH 2008513-001 PLASTIC DISPLAY COVER 100 ITALIAN 2010404-001 PLASTIC DISPLAY COVER, DPC300,...
  • Page 85 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2010368-001 PLASTIC DISPLAY COVER, DPC100, DANISH 2010354-001 PLASTIC DISPLAY COVER, DPC 300, JAPANESE 2010369-001 PLASTIC DISPLAY COVER, DPC400, NORWEGIAN 2010355-001 PLASTIC DISPLAY COVER, DPC 200, JAPANESE 2010370-001 PLASTIC DISPLAY COVER, DPC300, NORWEGIAN 2010356-001 PLASTIC DISPLAY COVER, DPC 100, JAPANESE 2008333-001 LABEL FASCIA PRO CARE 400 ENGLISH 2009407-001 LABEL FASCIA, NORWEGIAN 200...
  • Page 86 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2008422-001 LABEL, FASCIA, PRO CARE 300, SWEDISH 2009433-001 LABEL, FASCIA, CZECH 100 2008423-001 LABEL, FASCIA, PRO CARE 200, SWEDISH 2009434-001 LABEL, FASCIA, SLOVAK 400 2008424-001 LABEL, FASCIA, PRO CARE 100, SWEDISH 2009435-001 LABEL, FASCIA, SLOVAK 300 2008425-001 LABEL FASCIA PRO CARE 400 DUTCH 2009436-001 LABEL, FASCIA, SLOVAK 200 2008426-001...
  • Page 87 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2008806-001 LABEL, KEYPAD DPC300 SPANISH PRINTER 2008807-001 LABEL, KEYPAD DPC200 SPANISH PRINTER 2008808-001 LABEL, KEYPAD DPC100 SPANISH PRINTER 2010815-001 LABEL SET, KEYPAD DPC400,ENGLISH,PRINT,AUSC 2010816-001 LABEL SET, KEYPAD,DPC300,ENGLISH,PRINT,AUSC 2010817-001 LABEL SET, KEYPAD,DPC200,ENGLISH,PRINT,AUSC 2010818-001 LABEL SET, KEYPAD,DPC100,ENGLISH,PRINT,AUSC...
  • Page 88 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2009138-001 LABEL, KEYPAD DPC100 CHINESE PRINTER 2009147-001 LABEL, KEYPAD DPC400, DANISH, PRINTER 2009148-001 LABEL, KEYPAD, DPC300, DANISH, PRINTER 2009172-001 LABEL, KEYPAD, DPC100, PORTUGUESE, PRINTER 2009173-001 LABEL, KEYPAD, DPC400, RUSSIAN, PRINTER 2009175-001 LABEL, KEYPAD, DPC300, RUSSIAN, PRINTER 2009176-001...
  • Page 89 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2010735-001 LABEL,KEYPAD,DPC200,ENGLISH,PRINTERLESS 2010736-001 LABEL,KEYPAD,DPC100,ENGLISH,PRINTERLESS 2010737-001 LABEL,KEYPAD,DPC400,FRENCH,PRINTERLESS 2010738-001 LABEL,KEYPAD,DPC300,FRENCH,PRINTERLESS 2010739-001 LABEL,KEYPAD,DPC200,FRENCH,PRINTERLESS 2010740-001 LABEL,KEYPAD,DPC100,FRENCH,PRINTERLESS 2010741-001 LABEL,KEYPAD,DPC400,GERMAN,PRINERLESS 2010742-001 LABEL,KEYPAD,DPC300,GERMAN,PRINTERLESS 2010743-001 LABEL,KEYPAD,DPC200,GERMAN,PRINTERLESS 2010744-001 LABEL,KEYPAD,DPC100,GERMAN,PRINTERLESS 2010745-001 LABEL,KEYPAD,DPC400,SPANISH,PRINTERLESS 2010746-001 LABEL,KEYPAD,DPC300,SPANISH,PRINTERLESS 2010747-001 LABEL,KEYPAD,DPC200,SPANISH,PRINTERLESS 2010748-001 LABEL,KEYPAD,DPC100,SPANISH,PRINTERLESS 2010749-001 LABEL,KEYPAD,DPC400,ITALIAN,PRINTERLESS 2010750-001...
  • Page 90 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2010783-001 LABEL,KEYPAD,DPC300,FINNISH,PRINTERLESS 2010784-001 LABEL,KEYPAD,DPC200,FINNISH,PRINTERLESS 2010785-001 LABEL,KEYPAD,DPC100,FINNISH,PRINTERLESS 2010786-001 LABEL,KEYPAD,DPC400,PORTUGUESE,PRINTLESS 2010788-001 LABEL,KEYPAD,DPC300,PORTUGUESE,PRINTLESS 2010789-001 LABEL,KEYPAD,DPC200,PORTUGUESE,PRINTLESS 2010790-001 LABEL,KEYPAD,DPC100,PORTUGUESE,PRINTLESS 2010791-001 LABEL.KEYPAD,DPC400,RUSSIAN,PRINTERLESS 2010792-001 LABEL,KEYPAD,DPC300,RUSSIAN,PRINTERLESS 2010793-001 LABEL,KEYPAD,DPC200,RUSSIAN,PRINTERLESS 2010794-001 LABEL,KEYPAD,DPC100,RUSSIAN,PRINTERLESS 2010795-001 LABEL,KEYPAD,DPC400,HUNGARIAN,PRINTRLESS 2010796-001 LABEL,KEYPAD,DPC300,HUNGARIAN,PRINTRLESS 2010797-001 LABEL,KEYPAD,DPC200,HUNGARIAN,PRINTRLESS 2010798-001 LABEL,KEYPAD,DPC100,HUNGARIAN,PRINTRLESS 2010799-001...
  • Page 91 Parts List, Drawings, and Replacement: Service Parts Bubble Part Number Description Number 2010814-001 LABEL,KEYPAD,DPC100,GREEK,PRINTERLESS 2010819-001 LABEL,KEYPAD,DPC400,ENGLISH,AUSC,PRNTLSS 2010820-001 LABEL,KEYPAD,DPC300,ENGLISH,AUSC,PRNTLSS 2010821-001 LABEL,KEYPAD,DPC200,ENGLISH,AUSC,PRNTLSS 2010822-001 LABEL,KEYPAD,DPC100,ENGLISH,AUSC,PRNTLSS 2011830-001 KIT, FRU HELP CARD GUIDES ENGLISH 2018389-001 KIT, KEYPADS LEFT & RIGHT PROCARE FRU 2020006-001 PRINTER ROLLER 633178CR BATTERY, LEAD-ACID, 6-VOLT, 3.0 AH ®...
  • Page 92: Fru Main Reference Guide Drawing

    Parts List, Drawings, and Replacement: Service Parts FRU Main Reference Guide Drawing For quick reference use the following FRU Main Reference Guide drawing. ® 6-16 DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 93: Assembly/Disassembly Of Frus

    Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs Assembly/Disassembly of FRUs Monitor Disassembly Procedure The following procedure is sequential (i.e., you must remove the battery and rear case to remove the printer, etc. Battery Remove 4 screws securing the instruction cards. Remove the battery compartment door and adhesive pad.
  • Page 94 Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs Carefully remove the front faceplate. Remove 2 screws behind black overlay. Set monitor on its face and open the printer door. Carefully remove the rear case. Unplug speaker cable from circuit board. Unplug rear case cable.
  • Page 95 Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs Moves aside battery cables. Locate and release retention tab and slide back sub chassis. Lift the 2 black tabs and remove printer cable. Remove printer assembly. Remove sub-chassis and set aside. Remove pneumatic assembly from sub-chassis. ®...
  • Page 96: Spo2 Board

    Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs Board Remove hex nuts near SPO2 board. Turn monitor over and remove 2 SPO2 connector screws. Turn monitor on its face. Using needle nose pliers squeeze nylon retention tabs and remove SPO2 board.
  • Page 97: Display Board

    Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs Display Board Carefully lift the Main board away from the Display board. Collect the 5 spacers used to align the Main and Display Boards. Lift the display board away from the front panel. The monitor is now completely disassembled.
  • Page 98 Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs ® 6-22 DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 99: Technical Specifications

    Technical Specifications ® Revsion C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 100 For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 101: Specifications

    Technical Specifications: Specifications Specifications Mechanical Dimensions Height: 9.7 in (24.7 cm) Width: 8.6 in (21.9 cm) without Temperature 10.0 in (25.4 cm) with Temperature Depth: 5.3 in (13.5 cm) Weight, Including Battery 5.68 lb (2.58 kg) Mountings Self-supporting on rubber feet Portability Carried by handle Classification Information...
  • Page 102: Environmental

    Technical Specifications: Specifications Environmental Operating Temperature + 5 °C to + 40 °C (+ 41 °F to + 104 °F) Operating Atmospheric Pressure 700 hPa to 1060 hPa Storage Temperature – 20 °C to + 50 °C (– 4 °F to + 122 °F) Storage/Transportation Atmospheric Pressure 500 hPa to 1060 hPa...
  • Page 103: Critikon Us Patents

    Technical Specifications: Specifications All DINAMAP Monitor regulatory and accuracy studies have been performed ® using CRITIKON ® Blood Pressure Cuffs. Use only CRITIKON ® Blood Pressure Cuffs. The size, shape, and bladder characteristics can affect the performance of the instrument. Inaccurate readings may occur unless CRITIKON Blood Pressure Cuffs are used.
  • Page 104: Nellcor Sensor Accuracy

    Technical Specifications: Specifications ® **Applicability: OxiMax MAX-A, MAX-AL, MAX-P, MAX-I, and MAX-N sensors. ® NELLCOR Sensor Accuracy NOTE: All NELLCOR ® sensors must be used with the NELLCOR ® DOC-10 cable; the SCP-10 cable is not compatible with the ProCare Monitor. Sensor Model Range 70% - 100%...
  • Page 105: Factory Default Settings

    Technical Specifications: Specifications Power Dissipation Infrared: 22.5 mW (max) Red: 30 mW (max) Factory Default Settings HIGH Alarm Limit: 100 LOW Alarm Limit: 90 Response Mode 2 (for Mode 2: Fast Response) ™ SatSeconds ® NELLCOR Patents US Patent No. 4,802,486; 4,869,254; 4,928,692; 4,934,372; 5,078,136; 5,485,847; 5,743,263;...
  • Page 106: Masimo® Sensor Accuracy

    Technical Specifications: Specifications ® ‡The Masimo SET parameter 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.
  • Page 107: Temperature

    Technical Specifications: Specifications Temperature Scale °Fahrenheit (F) °Celsius (C) Range Predictive mode Max: 41.1° C; 106.0° F Min: 35.6° C; 96.0° F Monitor mode Max: 41.1° C; 106.0° F Min: 26.7° C; 80.0° F Monitor mode accuracy ± 0.1° C ±...
  • Page 108 Technical Specifications: Specifications ® A-10 DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 109 Appropriate Use of NIBP Simulators ® Revision C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 110 Appropriate Use of NIBP Simulators: For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 111: Appropriate Use Of Nibp Simulators

    NIBP monitors be established through clinical testing - the use of NIBP simulators is not acceptable. GE Healthcare has established accuracy using the AAMI SP-10 standard (2) and a similar standard exists in Europe (3). The AAMI standard specifies that the accuracy of NIBP monitors can be determined using either an invasive (intra- arterial) or noninvasive (auscultatory) blood pressure reference.
  • Page 112: What Do Simulator Manufactures Say

    Appropriate Use of NIBP Simulators: Appropriate Use of NIBP Simulators develop an algorithm, which produces readings that correspond to the simulator settings, it is preferable to use the clinical data for algorithm development. What Do Simulator Manufactures Say? The DNI Nevada (Fluke Biomedical) CuffLink manual states: "Since the CuffLink produces the same response independent of the inflate/ deflate cycle or the algorithm used by the monitor, we offer the term "Target Value"...
  • Page 113: Why Use Simulators

    Appropriate Use of NIBP Simulators: Appropriate Use of NIBP Simulators "Neither the monitor or the BP Pump 2 is broken. Some monitors were designed to give readings close to those obtained by the Auscultatory method of blood pressure determinations. Other monitors have been designed to agree with Invasive blood pressure readings.
  • Page 114 Figure 2B: Cuff Oscillation From A Simulator Measurement References FDA, CDRH, Non-Invasive Blood Pressure (NIBP) Monitor Guidance, March 10, 1997 ANSI/AAMI SP10:2002, Manual, Electronic or Automated Sphygmomanometers EN 1060-4 2004 Specification for non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers Mieke, S, Substitute of simulators for human subjects;...
  • Page 115: Electromagnetic Compatibility (Emc

    Electromagnetic Compatibility (EMC) ® Revision C DINAMAP ProCare Monitor Service Manual 2009381-001...
  • Page 116 Electromagnetic Compatibility (EMC): For your notes ® DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 117: Electromagnetic Compatibility (Emc): Procare Monitor

    Electromagnetic Compatibility (EMC): 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.
  • Page 118 Electromagnetic Compatibility (EMC): 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 ®...
  • Page 119 Electromagnetic Compatibility (EMC): 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 ®...
  • Page 120 Electromagnetic Compatibility (EMC): 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.
  • Page 121: Compliant Cables And Accessories

    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.
  • Page 122: Electromagnetic Compatibility (Emc): Ilc-1926

    Electromagnetic Compatibility (EMC): 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.
  • Page 123 Electromagnetic Compatibility (EMC): 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.
  • Page 124 Electromagnetic Compatibility (EMC): 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.
  • Page 125: Recommended Separation Distances

    Electromagnetic Compatibility (EMC): 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.
  • Page 126: Compliant Cables And Accessories

    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.
  • Page 127: Electromagnetic Compatibility (Emc): Ilc-1931

    Electromagnetic Compatibility (EMC): 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.
  • Page 128 Electromagnetic Compatibility (EMC): 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.
  • Page 129 Electromagnetic Compatibility (EMC): 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.
  • Page 130: Recommended Separation Distances

    Electromagnetic Compatibility (EMC): 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.
  • Page 131: Compliant Cables And Accessories

    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.
  • Page 132 Electromagnetic Compatibility (EMC): Electromagnetic Compatibility (EMC): ILC-1931 ® C-18 DINAMAP ProCare Monitor Service Manual Revision C 2009381-001...
  • Page 134 Tel: + 86 21 5257 4650 Fax:+ 1 414 355 3790 Fax: + 49 761 45 43 - 233 Fax: + 86 21 5208 2008 GE Medical Systems Information Technologies, a General Electric Company, going to market as GE Healthcare www.gehealthcare.com 0086...

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