GE Healthcare DINAMAP™ ProCare Monitor Service Manual DINAMAP ProCare Monitor English 2009381-001D (paper) © 2005-2008 General Electric Company. All Rights Reserved.
GE Healthcare DINAMAP™ ProCare Monitor Service Manual DINAMAP ProCare Monitor English 2009381-001D (paper) © 2005-2008 General Electric Company. All Rights Reserved.
GUARANTEE All equipment sold by GE Medical Systems Information Technologies, is fully guaranteed as to materials and workmanship for a specified period. Refer to your warranty for more information. GE Medical Systems Information Technologies reserves the right to perform guarantee service operations in its own factory, at an authorized repair station, or in the customer’s installation.
Contents 1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1 Revision History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Manual Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Ordering Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Safety Information . . . . . . . . . . . . . . . . . . . . . . .
2 Equipment Overview . . . . . . . . . . . . . . . . . . . . . . . . . 2-1 Equipment Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3 Product Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3 Basic Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4 Front Panel Controls and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Host Communications Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13 DB15 Connector Pin Assignments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13 Connection Details . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13 4 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1 Preventative Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
SpO2 Circuit Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-16 Test Results Form . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-17 5 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1 Alarm Code Interpretation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3 System Failures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Accuracy and Motion Tolerance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Saturation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Pulse Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . NELLCOR® Sensor Accuracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Factory Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
vi DINAMAP® ProCare Monitor 2009381-001 Revision D
1 Revision D Introduction DINAMAP® ProCare Monitor 2009381-001 1-1
For your notes 1-2 DINAMAP® ProCare Monitor 2009381-001 Revision D
Introduction: Revision History Revision History Each page of this manual has a revision letter located at the bottom of the page. This letter identifies the revision level of the entire manual. This may be important if you have different manuals and you do not know which is the most current. For the initial release, all pages have the revision letter A. For the second update, all pages receive the revision letter B.
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; and the monitor is used in accordance with the instructions of use.
Introduction: Safety Information Warnings, Cautions, and Notes The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level or seriousness. Familiarize yourself with their definitions and significance. Hazard is defined as a source of potential injury to a person. DANGER indicates an imminent hazard which, if not avoided, will result in death or serious injury.
Introduction: Equipment Symbols The ProCare Monitor is designed to conform to Electromagnetic Compatibility (EMC) standard IEC 60601-1-2 and will operate accurately in conjunction with other medical equipment which also meets this requirement. To avoid interference problems affecting the Monitor, do not use the Monitor in the presence of equipment which does not conform to these specifications. Place the ProCare Monitor on a rigid, secure surface.
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 Manufacturer: This symbol is accompanied by the name and the address of the manufacturer. Manufacturing Date: This symbol is accompanied by the date of the manufacturing. European authorized representative.
Introduction: Service Requirements The DINAMAP® ProCare Monitor is protected against vertically falling drops of water and conforms with the IEC 529 standard at level of IPX1. Vertically falling drops shall have no harmful effects to the Monitor. IPX1 Service Requirements Follow the service requirements listed below. Refer equipment servicing to GE Medical Systems Information Technologies authorized service personnel only.
Introduction: Intended Audience Intended Audience This manual is intended for service representatives and technical personnel who maintain, troubleshoot, or repair this equipment. Intended Use General Use The ProCare Monitor is intended to monitor one patient at a time in a clinical setting. Federal law (U.S.A.) restricts this device to sale by or on the order of a physician.
Introduction: Service Policy ensure that they are not the cause of the problem. If you are unable to resolve the problem after checking these items, contact GE Medical Systems Information Technologies.
Introduction: Disposal of Product Waste Service No Charge Rental A no charge rental unit is provided at no charge during the warranty period of the product when we perform the repair service. GE Medical Systems Information Technologies pays the shipping charges for a loaner sent to the customer for product repairs under the warranty. Rental units are available in non-warranty situations. The customer pays the shipping charges to return a rental.
Introduction: Disposal of Product Waste Patient Applied Parts Certain patient applied parts, such as those with adhesive (disposable SpO2 sensors), are intended for single use and should be disposed of properly as medical waste in accordance with regional body controlled guideline. Other patient applied parts, such as blood pressure cuffs, should be cleaned according to instructions.
2 Revision D Equipment Overview DINAMAP® ProCare Monitor 2009381-001 2-1
For your notes 2-2 DINAMAP® ProCare Monitor 2009381-001 Revision D
Equipment Overview: Equipment Description Equipment Description The ProCare Monitor provides a small, portable, easy-to-use monitoring alternative for sub-acute hospital and non-hospital settings. The DC-operated Monitor offers noninvasive determination of systolic blood pressure, diastolic blood pressure, mean arterial pressure, pulse rate, oxygen saturation, and temperature. Monitors are available with or without integrated printers.
Equipment Overview: Basic Components Basic Components Front Panel Controls and Indicators Buttons 2-4 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.
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. Refer to the History section of this manual for more information. 12. Print button: Press to print currently displayed values or all stored entries when in history mode. 13.
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. 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.
Equipment Overview: Product Compliance Product Compliance The DINAMAP® ProCare Monitor is classified in the following categories for compliance with IEC 60601-1: Internally powered or Class II when powered from external supply Transportable For continuous operation Not suitable for use in the presence of flammable anesthetics Not for use in the presence of an oxygen-enriched atmosphere (oxygen tent) Type BF applied parts IPX1, degree of protection against ingress of water Ste
Equipment Overview: Theory of Operation Theory of Operation Introduction This section provides overall theory of operation and functional description of the ProCare Monitor.
Equipment Overview: Overall Principles of Operation 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 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. The results are digitized and sent to the Main Board via opto couplers. The couplers provide patient isolation as well as serial data interface.
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. The figure shows the NIBP determination sequence. NIBP Determination Sequence At each step the microprocessor stores cuff pressure, the matched pulse amplitude, and the time between successive pulses.
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.
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. The Turbo Temp probe also contains a thermistor that indicates the temperature.
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.
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.
Revision D DINAMAP® ProCare Monitor 2009381-001 Host Comm Port(rear) Temp Probe (optional) BP Cuff SpO2 Probe (Optional) Tubing Control Tubing Control/Data RS 232 Remote Alarm Optical Switch Temp Control/Data Pump/Valve Manifold SpO2 Circuit Unit Block Diagram Speaker Audio Control Temp Control Interface Printer Control/Data Printer Driver Isolated DC Power Supply PT1/PT2 NIBP Data Main Board External DC 6V Battery Display LEDS Switches UI Board Equipment Overview: Functional Desc
Equipment Overview: Functional Description 2-16 DINAMAP® ProCare Monitor 2009381-001 Revision D
3 Revision D Installation DINAMAP® ProCare Monitor 2009381-001 3-1
For your notes 3-2 DINAMAP® ProCare Monitor 2009381-001 Revision D
Installation: Connections Connections Rear Panel 1 1. Data interface connector: Host communications port (15 pin D-type RS-232 serial port) for use only with equipment conforming to IEC 60601-1, configured to comply with IEC 60601-1-1. Right-Side Panel 2 2. Revision D External DC power socket: To be used with approved GE Medical Systems Information Technologies AC-DC power converter ONLY.
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. The Monitor automatically senses if the battery needs recharging.
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. NEVER allow the battery to become completely discharged. A fully charged battery will power the Monitor for approximately 5 hours. To ensure optimum operation (full charge cycles), replace only with a recommended battery.
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. All parameters are available for monitoring in this mode.
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 1st configuration mode page (displaying CFG). You can use the + and - buttons to make changes to settings. After making changes, simply cycle the power to return to normal operation (clinical) mode. Changes are automatically retained. The Menu selections appear in the following order.
Installation: Configuring Your ProCare Monitor Inflation Pressure Default Setting – Procedures 1. 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. 2. Use the +/- buttons to increment or decrement the inflate pressure default setting. Increments are 5mmhg from 100mmhg to 250mmhg.
Installation: Configuring Your ProCare Monitor Procedure for units with Masimo® Technology (Refer to the Masimo® section for options) 1. 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. 2. Press the Menu button until n0d appears in the Pulse Rate window. 3. Use the +/- buttons to select the option. 4. Press the Menu button once. SAt appears in the Pulse Rate window. 5.
Installation: Configuring Your ProCare Monitor The advanced configuration mode option pages are as follows: Displayed on Monitor ACF Function Advanced Configuration Mode announcement (No settings are entered on this page.) rEM Remote mode 0 : Remote mode is disabled 1 : Remote mode is enabled Adr Host Comm unit address 32 : This is the default value.
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” operation is executed (on the final Service Mode options page).
Installation: Configuring Your ProCare Monitor Displayed on Monitor Function 6 (in “min” window) Language In “MAP/Cuff” window: The number displayed in Pulse Rate display window indicates the language setting. These range from 0 to 20. For example, 0 indicates English. The language setting is used in printed reports. # of remaining saves possible.
Installation: Host Communications Connector Host Communications Connector All host port signals are NON-ISOLATED and should be connected to equipment conforming to IEC 60601-1-1 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.
Installation: Host Communications Connector Pin # 3-14 Function 1 Common 2 Inverted TTL Transmit Data 3 Inverted TTL Receive Data 4 +5 volts 5 No connection 6 No connection 7 Common 8 Remote Alarm 9 No connection 10 No connection 11 RS232 Transmit Data (TxD) 12 No connection 13 RS232 Receive Data (RxD) 14 No connection 15 No connection DINAMAP® ProCare Monitor 2009381-001 Revision D
4 Revision D Maintenance DINAMAP® ProCare Monitor 2009381-001 4-1
For your notes 4-2 DINAMAP® ProCare Monitor 2009381-001 Revision D
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.
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” around connection pins. Never immerse monitor or accessories in any liquid. Do not attach the monitor or accessories to a patient until it is thoroughly dry.
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. Never spray the glass cleaner directly onto the display, and never use alcohol or petroleum based products. Cuffs General The cuff must be thoroughly cleaned with the specified detergent before reuse.
Maintenance: Long-Term Storage 3. Spray the 10% bleach solution on the affected area until the area is saturated. Allow the cuff to sit for 5 minutes. 4. Wipe away any excess solution and rinse the cuff again with distilled water. 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.
Maintenance: Long-Term Storage Battery Care If it becomes necessary to store the Monitor for an extended period of time, first fully charge, then remove the battery. Then store the Monitor and the battery in the original packaging materials. Batteries should always be fully charged before being placed in storage. Batteries should not be left in storage more than 6 months without removal and full recharge.
Maintenance: Long-Term Storage Replacing the Battery 1. Unplug the Monitor from the DC power source. 2. 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. 3. Remove the help card tray and battery door cover. 4. Remove the old battery and disconnect the wires.
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. Fuses The Monitor contains four fuses. The fuses are auto-resettable and mounted within the Monitor.
Maintenance: Parameter Level Functional Testing Calibration Procedures and Tests NOTE:All devices are tested and calibrated during manufacturing and are certified for operation at installation.
Maintenance: Parameter Level Functional Testing 3. 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. 1. Turn unit on and enter Service Mode. 2. Press Cycle button and 1 should appear in the min window. 3. Close the valve on the inflation bulb. 4. Using the inflation bulb, inflate the system to 210 mmHg. 5.
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. 1. Turn unit on and enter Service Mode. 2. The min window should display 0. 3. Open the valve on the inflation bulb and remove all pressure from the system (manometer reads zero). 4. Press Cycle button and 1 should appear in the min window. 5.
Maintenance: Parameter Level Functional Testing 6. Close valve on bulb and slowly inflate pressure to 200 mmHg (using the manometer as reference). 7. Press Menu button when pressure reads exactly 200 mmHg to save calibration setting. 8. Press Cycle button until 6 appears in the min window. 9. Press and hold Menu button until monitor beeps, which acknowledges that data was saved. 10. Turn the Monitor off.
Maintenance: Parameter Level Functional Testing External DC Verification 1. Plug the power brick into the Monitor. 2. 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. 1.
Maintenance: Parameter Level Functional Testing Alaris Turbo Temp Probe Date Code 1. Turn Monitor off. Make sure the temp probe is properly stored in the probe well. 2. Disconnect the temp probe cable from the monitor. 3. Connect Temp simulator; set to 80.2°F. 4. Turn the Monitor on. 5. Put the Monitor into temp monitor mode: a. partially remove the probe from the well (stop when you hear the Monitor beep). b.
Maintenance: Parameter Level Functional Testing SpO2 (Perform only if equipped with SpO2 module) 1. Connect the appropriate SpO2 probe and cable to the SpO2 connector. Place the probe on your finger. 2. Verify the unit displays a: Pulse value Saturation value Signal Strength Bar Graph 3. Remove the sensor from your finger to generate an E23 alarm and to sound the speaker. 4. Press the Silence button. 5. Verify the sound has stopped and the E23 error is cleared. 6.
Maintenance: Test Results Form Test Results Form 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
Maintenance: Test Results Form Description Min Max Temperature reading at 80.2° F 79.9° F 80.5° F Temperature reading at 98.6° F 98.4° F 98.8° F Temperature reading at 107.8° F 107.5° F 108.
5 Revision D Troubleshooting DINAMAP® ProCare Monitor 2009381-001 5-1
For your notes 5-2 DINAMAP® ProCare Monitor 2009381-001 Revision D
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. 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.
Troubleshooting: Alarm Code Interpretation 8. The SPO2 window shows the Time the error occurred. 9. 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 or Problem Source Display blank, high pitch alarm System 930 5-4 Definition Can be Silenced? Probable Source Failsafe error No Mains PWA issue SPO2 No status from module for 30 ±10 sec.
Troubleshooting: Alarm Code Interpretation Error Code or Problem Source E13 Battery E21 SPO2 Failed SPO2 sensor E23 SPO2 SPO2 Sensor off finger Yes Reposition SPO2 sensor E25 SPO2 SPO2 No signal Yes Reposition SPO2 sensor E61 Temp Temp probe failure No Replace temperature probe E63 Temp Probe disconnected or wrong type Yes Check for correct probe E66 Temp Temperature probe too hot No Replace probe E80 NIBP Overpressure Yes Check for pinched or occluded internal tubing E
Troubleshooting: Alarm Code Interpretation 5-6 DINAMAP® ProCare Monitor 2009381-001 Revision D
6 Revision D Parts List, Drawings, and Replacement DINAMAP® ProCare Monitor 2009381-001 6-1
For your notes 6-2 DINAMAP® ProCare Monitor 2009381-001 Revision D
Parts List, Drawings, and Replacement: Ordering Parts 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.
Parts List, Drawings, and Replacement: Service Parts Part Part Number BP: Air Hose 12-ft Adult/Pediatric, Screw Connector 107365 Air Hose 24-ft Adult/Pediatric, Screw Connector 107366 Air Hose 12 ft Neonatal 107368 SENSA-CUF® 2-Tube Screw Connector, Infant 2458 SENSA-CUF® 2-Tube Screw Connector, Child 2460 SENSA-CUF® 2-Tube Screw Connector, Sm. Adult 2462 SENSA-CUF® 2-Tube Screw Connector, Adult 2464 SENSA-CUF® 2-Tube Screw Connector, Lg.
Parts List, Drawings, and Replacement: Service Parts Part Part Number SPO2: 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. ***Masimo is a trademark of Masimo Corporation.
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.
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 20 2010478-001 KIT, FRU, LABEL, ENGLISH, DPC300, PRINT 20 2010479-001 KIT, FRU, LABEL, ENGLISH, DPC200, PRINT 20 2010480-001 KIT, FRU, LABEL, ENGLISH, DPC100, PRINT 21 2011645-001 FRU PROCARE ENGLISH KEYPAD LABEL SET, 100-400 20 2008329-001 PLASTIC DISPLAY COVER 400 ENGLISH 2010371-001 PLASTIC DISPLAY COVER, DPC200, NORWEGIAN 20 2008330-001 PLASTIC DISPLAY COVER 300 ENGLISH 2010372-001 PLASTIC DISPLAY COVER, D
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number Description 20 2008510-001 PLASTIC DISPLAY COVER 400 ITALIAN 2010401-001 PLASTIC DISPLAY COVER, DPC200, HUNGARIAN 20 2008511-001 PLASTIC DISPLAY COVER 300 ITALIAN 2010402-001 PLASTIC DISPLAY COVER, DPC100, HUNGARIAN 20 2008512-001 PLASTIC DISPLAY COVER 200 ITALIAN 2010403-001 PLASTIC DISPLAY COVER, DPC400, CZECH 20 2008513-001 PLASTIC DISPLAY COVER 100 ITALIAN 2010404-001 PLASTIC DISPLAY COVER, DPC300, CZECH 20 2
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 20 2010368-001 PLASTIC DISPLAY COVER, DPC100, DANISH 2010354-001 PLASTIC DISPLAY COVER, DPC 300, JAPANESE 20 2010369-001 PLASTIC DISPLAY COVER, DPC400, NORWEGIAN 2010355-001 PLASTIC DISPLAY COVER, DPC 200, JAPANESE 20 2010370-001 PLASTIC DISPLAY COVER, DPC300, NORWEGIAN 2010356-001 PLASTIC DISPLAY COVER, DPC 100, JAPANESE 20 2008333-001 LABEL FASCIA PRO CARE 400 ENGLISH 2009407-001 LABEL FASCIA, NORWEGIAN 200 20 2
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 20 2008422-001 LABEL, FASCIA, PRO CARE 300, SWEDISH 2009433-001 LABEL, FASCIA, CZECH 100 20 2008423-001 LABEL, FASCIA, PRO CARE 200, SWEDISH 2009434-001 LABEL, FASCIA, SLOVAK 400 20 2008424-001 LABEL, FASCIA, PRO CARE 100, SWEDISH 2009435-001 LABEL, FASCIA, SLOVAK 300 20 2008425-001 LABEL FASCIA PRO CARE 400 DUTCH 2009436-001 LABEL, FASCIA, SLOVAK 200 20 2008426-001 LABEL FASCIA PRO CARE 300 DUTCH 2009438-001 LAB
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 21 2008806-001 LABEL, KEYPAD DPC300 SPANISH PRINTER 21 2008807-001 LABEL, KEYPAD DPC200 SPANISH PRINTER 21 2008808-001 LABEL, KEYPAD DPC100 SPANISH PRINTER 21 2010815-001 LABEL SET, KEYPAD DPC400,ENGLISH,PRINT,AUSC 21 2010816-001 LABEL SET, KEYPAD,DPC300,ENGLISH,PRINT,AUSC 21 2010817-001 LABEL SET, KEYPAD,DPC200,ENGLISH,PRINT,AUSC 21 2010818-001 LABEL SET, KEYPAD,DPC100,ENGLISH,PRINT,AUSC 21 2010823-001
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 21 2009138-001 LABEL, KEYPAD DPC100 CHINESE PRINTER 21 2009147-001 LABEL, KEYPAD DPC400, DANISH, PRINTER 21 2009148-001 LABEL, KEYPAD, DPC300, DANISH, PRINTER 21 2009172-001 LABEL, KEYPAD, DPC100, PORTUGUESE, PRINTER 21 2009173-001 LABEL, KEYPAD, DPC400, RUSSIAN, PRINTER 21 2009175-001 LABEL, KEYPAD, DPC300, RUSSIAN, PRINTER 21 2009176-001 LABEL, KEYPAD, DPC200, RUSSIAN, PRINTER 21 2009177-001 LABEL, KEY
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 21 2010735-001 LABEL,KEYPAD,DPC200,ENGLISH,PRINTERLESS 21 2010736-001 LABEL,KEYPAD,DPC100,ENGLISH,PRINTERLESS 21 2010737-001 LABEL,KEYPAD,DPC400,FRENCH,PRINTERLESS 21 2010738-001 LABEL,KEYPAD,DPC300,FRENCH,PRINTERLESS 21 2010739-001 LABEL,KEYPAD,DPC200,FRENCH,PRINTERLESS 21 2010740-001 LABEL,KEYPAD,DPC100,FRENCH,PRINTERLESS 21 2010741-001 LABEL,KEYPAD,DPC400,GERMAN,PRINERLESS 21 2010742-001 LABEL,KEYPAD,
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 21 2010783-001 LABEL,KEYPAD,DPC300,FINNISH,PRINTERLESS 21 2010784-001 LABEL,KEYPAD,DPC200,FINNISH,PRINTERLESS 21 2010785-001 LABEL,KEYPAD,DPC100,FINNISH,PRINTERLESS 21 2010786-001 LABEL,KEYPAD,DPC400,PORTUGUESE,PRINTLESS 21 2010788-001 LABEL,KEYPAD,DPC300,PORTUGUESE,PRINTLESS 21 2010789-001 LABEL,KEYPAD,DPC200,PORTUGUESE,PRINTLESS 21 2010790-001 LABEL,KEYPAD,DPC100,PORTUGUESE,PRINTLESS 21 2010791-001 LAB
Parts List, Drawings, and Replacement: Service Parts Bubble Number Part Number 21 2010814-001 LABEL,KEYPAD,DPC100,GREEK,PRINTERLESS 21 2010819-001 LABEL,KEYPAD,DPC400,ENGLISH,AUSC,PRNTLSS 21 2010820-001 LABEL,KEYPAD,DPC300,ENGLISH,AUSC,PRNTLSS 21 2010821-001 LABEL,KEYPAD,DPC200,ENGLISH,AUSC,PRNTLSS 21 2010822-001 LABEL,KEYPAD,DPC100,ENGLISH,AUSC,PRNTLSS 22 2011830-001 KIT, FRU HELP CARD GUIDES ENGLISH 23 2018389-001 KIT, KEYPADS LEFT & RIGHT PROCARE FRU 24 2020006-001 PRINTER ROLLE
Parts List, Drawings, and Replacement: Service Parts FRU Main Reference Guide Drawing 5, 6 12 6-16 DINAMAP® ProCare Monitor 2009381-001 12 13,5,24 5 15 5,6 5,6,7 5,6,7 12 14 25 5,6 12 12 18 12 14 14 12 14 19 14 14 12 12 14 12 5,6 12 8,9,10 2,3 12 4 5,6 12 12 23 20 21 23 5,6 20 1 For quick reference use the following FRU Main Reference Guide drawing.
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 1. Remove 4 screws securing the instruction cards. 2. Remove the battery compartment door and adhesive pad. 3. The battery can now be removed. 1. Remove remaining four screws from the bottom of the monitor. 2. Set monitor upright.
Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs 3. Carefully remove the front faceplate. 4. Remove 2 screws behind black overlay. 5. Set monitor on its face and open the printer door. 6. Carefully remove the rear case. 7. Unplug speaker cable from circuit board. 8. Unplug rear case cable. 1. Unplug air hose from valve and 2 elbow joints. 2. Remove 3 cable assemblies.
Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs Revision D 3. Moves aside battery cables. 4. Locate and release retention tab and slide back sub chassis. 5. Lift the 2 black tabs and remove printer cable. 6. Remove printer assembly. 7. Remove sub-chassis and set aside. 8. Remove pneumatic assembly from sub-chassis.
Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs SpO2 Board 1. Remove hex nuts near SPO2 board. 2. Turn monitor over and remove 2 SPO2 connector screws. 3. Turn monitor on its face. 4. Using needle nose pliers squeeze nylon retention tabs and remove SPO2 board. 1. Remove 5 phillips screws. 2. Remove 2 torques head screws. 3. Unplug tubing from main bd.
Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs Display Board 1. Carefully lift the Main board away from the Display board. 2. Collect the 5 spacers used to align the Main and Display Boards. 3. Lift the display board away from the front panel. 4. The monitor is now completely disassembled. 5. Reverse the above sequence to reassemble the monitor. 6. Be careful not to pinch any cables or tubing during reassembly.
Parts List, Drawings, and Replacement: Assembly/Disassembly of FRUs 6-22 DINAMAP® ProCare Monitor 2009381-001 Revision D
A Revision D Technical Specifications DINAMAP® ProCare Monitor 2009381-001 A-1
For your notes A-2 DINAMAP® ProCare Monitor 2009381-001 Revision D
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.
Technical Specifications: Specifications Environmental Operating Temperature Operating Atmospheric Pressure Storage Temperature + 5 °C to + 40 °C (+ 41 °F to + 104 °F) 700 hPa to 1060 hPa – 20 °C to + 50 °C (– 4 °F to + 122 °F) Storage/Transportation Atmospheric Pressure 500 hPa to 1060 hPa Humidity Range 5% to 95% noncondensing Radio Frequency Complies with IEC Publication 60601-1-2 Medical Electrical Equipment, Electromagnetic Compatibility Requirements and Tests and CISPR 11 (Group 1, Class B) fo
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.
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 SpO2 Range 70% - 100% OxiMax® MAX-A*, MAX-AL* MAX-N*† (Adult) MAX-N*† (Neonate) MAX-P* MAX-I* MAX-R*‡ ±2 digits ±2 digits ±3 digits ±2 digits ±2 digits ±3.
Technical Specifications: Specifications Power Dissipation Infrared: 22.5 mW (max) Red: 30 mW (max) SpO2 (%) SpO2 (%) Response Mode SatSeconds™ HIGH Alarm Limit: 100 LOW Alarm Limit: 90 2 (for Mode 2: Fast Response) 0 Factory Default Settings 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; 5,865,736; 6,035,223; 6,298,252; 6,463,310; 6,591,123; 6,675,031; 6,708,049; 6,801,797; Re. 35,122 and foreign equivalents.
Technical Specifications: Specifications ‡The Masimo SET® SpO2 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.
Technical Specifications: Specifications Temperature Scale °Fahrenheit (F) °Celsius (C) Range Predictive mode Monitor mode Max: 41.1° C; 106.0° F Min: 35.6° C; 96.0° F Max: 41.1° C; 106.0° F Min: 26.7° C; 80.0° F Monitor mode accuracy ± 0.1° C ± 0.2° F (when tested in a calibrated liquid bath; meets ASTM E1112, Table 1, in range specified) Determination time approx. 10 seconds, typical Use only IVAC® probes and P850A probe covers.
Technical Specifications: Specifications A-10 DINAMAP® ProCare Monitor 2009381-001 Revision D
B Revision D Appropriate Use of NIBP Simulators DINAMAP® ProCare Monitor 2009381-001 B-1
For your notes Revision D DINAMAP® ProCare Monitor 2009381-001 B-2
Appropriate Use of NIBP Simulators: Appropriate Use of NIBP Simulators Appropriate Use of NIBP Simulators NIBP Accuracy Noninvasive Blood Pressure (NIBP) monitors are approved for sale in the U.S. by the FDA (1) and in Europe through the CE Mark. Both of these processes require that the accuracy of NIBP monitors be established through clinical testing - the use of NIBP simulators is not acceptable.
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.
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.
Figure 2B: Cuff Oscillation From A Simulator Measurement References 1. FDA, CDRH, Non-Invasive Blood Pressure (NIBP) Monitor Guidance, March 10, 1997 2. ANSI/AAMI SP10:2002, Manual, Electronic or Automated Sphygmomanometers 3. EN 1060-4 2004 Specification for non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers 4.
C Revision D Electromagnetic Compatibility (EMC) DINAMAP® ProCare Monitor 2009381-001 C-1
For your notes Revision D DINAMAP® ProCare Monitor 2009381-001 C-2
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.
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 assure that the DINAMAP® ProCare Monitor is used in such an environment.
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 assure that the DINAMAP® ProCare Monitor is used in such an environment.
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.
Electromagnetic Compatibility (EMC): Electromagnetic Compatibility (EMC): ProCare Monitor Compliant Cables and Accessories CAUTION 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.
Electromagnetic Compatibility (EMC): Electromagnetic Compatibility (EMC): ProCare Monitor C-8 DINAMAP® ProCare Monitor 2009381-001 Revision D
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