GE Healthcare CARESCAPE™ V100 Vital Signs Monitor Service Manual Silence Systolic HIGH ADULT LOW Alarms Diastolic Inflate/Stop MAP/Cuff NEONATE HIGH Cycle AUTO CYCLE HISTORY History LOW To clear hold 2 seconds Menu INFLATE PRESSURE ALARM VOLUME PULSE VOLUME SpO Pulse Rate BATTERY OK HIGH LOW HIGH LOW Print BATTERY LOW CHARGING Temperature On / Off C F CARESCAPE V100 Vital Signs Monitor English 2037107-002 (CD) 2048724-002 (paper) © 2010, 2011 General Electric Company.
NOTE: The information in this manual applies to CARESCAPE V100 Vital Signs Monitor software version R1.5. Due to continuing product innovation, specifications in this manual are subject to change without notice. NOTE: For technical documentation purposes, the abbreviation GE is used for the legal entity name, GE Medical Systems Information Technologies, Inc. Listed below are GE Medical Systems Information Technologies, Inc. trademarks.
Contents 1 Introduction . . . . . . . . . . . . . . . . . . . . . . 1-1 Revision history . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2 Manual purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2 Intended audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2 Ordering manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2 Equipment overview . . . . . . . . . . . . . . . 2-1 Equipment description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2 Product configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2 Front controls and connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3 Front panel indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
When about 5 minutes of main battery charge remains: . . . . . . . . .3-4 When 5 minutes of main battery charge expires: . . . . . . . . . . . . . . . .3-4 After plugging the monitor into DC power: . . . . . . . . . . . . . . . . . . . . . .3-4 E13 BATTERY LOW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4 Configuring the monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5 Operating modes . . . . . . . . . . . .
Calibration procedures and tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Parameter test procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . NIBP tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Pneumatic leakage testing . . . . . . . . . . . . . . . . . . . . . . . .
6 Parts lists and drawings . . . . . . . . . . . 6-1 Ordering parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2 Compatible service parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2 NIBP accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-2 SpO2 - Ohmeda accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Ohmeda SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5 Nellcor SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7 Masimo SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-10 Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-13 Battery . . . . . . . .
1 2048723-002D Introduction CARESCAPE V100 Vital Signs Monitor 1-1
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: Conventions used in this manual Conventions used in this manual Within this manual, special styles and formats are used to distinguish between terms viewed on screen, a button you must press, or a list of menu commands you must select: For technical documentation purposes, the abbreviation GE is used for the legal entity names, GE Medical Systems Information Technologies, Inc. In this manual, the CARESCAPE V100 vital signs monitor is referred to as the monitor.
Introduction: Safety information Safety information The information presented in this section is important for the safety of both the patient and operator. This chapter describes how the terms Danger, Warning, Caution, and Note are used throughout the manual. In addition, standard equipment symbols are defined.
Introduction: Safety information Dangers, warnings, cautions, and notes The terms Danger, Warning, Caution and Note 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 a hazardous situation that, if not avoided, will result in death or serious injury.
Introduction: Safety information WARNING Only use the monitor in areas where adequate ventilation exists. WARNING Arrange the external AC/DC power converter, air hoses, and all cables carefully so they do not constitute a hazard. WARNING If powering the monitor from an external power adapter or converter, use only GE-approved power adapters and converters. WARNING The speaker is tested during unit power-up. If the power-up tones are not heard, audible alarms will also not be heard.
Introduction: Safety information WARNING Do not short-circuit the battery terminals by directly connecting the metal terminals together. Be certain that no metal objects (e.g., coins, paper clips, etc.) touch both battery terminals simultaneously. Doing so can cause the battery to overheat and/or explode, resulting in possible caustic burns and/or battery damage. WARNING Do not use any battery other than a GE-recommended battery.
Introduction: Safety information WARNING Use of portable phones or other radio frequency (RF) emitting equipment near the monitor may cause unexpected or adverse operation. WARNING Verify calibration of NIBP parameter (temperature and pulse oximeter do not require calibration; refer to the “Maintenance” section for instructions). Ensure that the display is functioning properly before operating the monitor. WARNING Keep the Exergen scanner secured when it is not in use.
Introduction: Safety information CAUTION Magnetic and electrical fields are capable of interfering with the proper performance of the monitor. For this reason make sure that all external devices operated in the vicinity of the monitor comply with the relevant EMC requirements. CAUTION The monitor does not include any user-replaceable fuses. Refer servicing to qualified service personnel. CAUTION Do not use replacement batteries other than the type supplied with the monitor.
Introduction: Equipment symbols CAUTION To prevent cross-contamination, clean exterior surfaces of the monitor, monitor accessories, and reusable sensors on a regular basis in compliance with your institution’s infection control unit and/or biomedical department’s local policy. CAUTION Do not sterilize the monitor by irradiation, gas-, heat- or chemical-based sterilization. NOTE This equipment is suitable for use in the presence of electrosurgery.
Introduction: Equipment symbols This product conforms with the essential requirements of the Medical Device Directive 93/42/EEC. Accessories without the CE mark are not guaranteed to meet the Essential Requirements of the Medical Device Directive. Charging Class II equipment Consult instructions for use. Defibrillator-proof type BF equipment European authorized representative External communications port connector External DC power input Fragile. Handle with care. Humidity limitations.
Introduction: Equipment symbols CAUTION — Safety ground precaution. Remove power cord from the mains source by grasping the plug. Do not pull on the cable. Catalog or orderable part number. Russia only. GOST-R mark. Prescriptive Device. USA only. For use by or on the order of a Physician, or persons licensed by state law. Device serial number.
Introduction: Service requirements Service requirements Follow the service requirements listed below. Refer equipment servicing to GE-authorized service personnel only. 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 or to one of GE’s authorized agents.
Introduction: Related manuals Related manuals Manual Title 2010566 Host Communications Reference Manual. Contact your GE sales representative or distributor. 2048723-001 CARESCAPE V100 Vital Signs Monitor Operator’s Manual (English). Contact your GE sales representative for information on other available languages. Service policy The warranty for this product is enclosed with the product in the shipper carton.
Introduction: Disposal of product waste The representative will record all necessary information and will provide a Return Authorization Number. Prior to returning any product for repair, a Return Authorization Number must be obtained. Packing instructions If you have to return goods for service, follow these recommended packing instructions. Remove all hoses, cables, sensors, and power cords from the monitor before packing.
Introduction: Disposal of product waste Batteries WARNING Do not incinerate the battery or expose it to fire or high temperatures. Doing so may cause the battery to explode. The sealed, rechargeable main battery contains lead and can be recycled. The rechargeable battery is of the sealed lead-acid form. Discharge this battery prior to disposal. Place the battery in packaging which electrically isolates its contents. Do not puncture or place the battery in a trash compactor.
2 2048723-002D Equipment overview CARESCAPE V100 Vital Signs Monitor 2-1
Equipment overview: Equipment description Equipment description The CARESCAPE V100 vital signs monitor provides a small, portable, easy-to-use monitoring alternative for sub-acute hospital and non-hospital settings. The monitor is for use on adult, pediatric, or neonatal patients—one at a time. The battery-operated monitor offers noninvasive determination of systolic blood pressure, diastolic blood pressure, mean arterial pressure, pulse rate, oxygen saturation, and temperature.
Equipment overview: Front controls and connectors Front controls and connectors 1. Silence button: mutes audible alarms. Any other active alarm that can be acknowledged is also cleared and the alarm condition is reset whenever this key is pressed. When pressed, the alarm silence indicator (bell) lights solid red to indicate that audible alarms have been silenced for 2 minutes. Alarm silence can be cancelled by pressing the Silence button again. 2.
Equipment overview: Front panel indicators 9. Cycle button: used to select NIBP mode of manual, auto cycle, or Stat mode. 10. Temperature probe cover storage: stores Alaris probe covers. 11. History button: activates 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. 12. Print button: prints currently displayed values or all stored entries when in history mode. 13.
Equipment overview: Right-side panel 21. Pulse Rate window: shows pulse rate in beats per minute. 22. SpO2 pulse indicator: flashing red LED bar indicates that pulses are being derived from SpO2 signals. 23. SpO2 window: indicates oxygen saturation in %. 24. MAP/Cuff window: indicates measured mean arterial pressure (MAP) in mmHg and shows cuff pressure during NIBP determination. 25. ADULT indicator: lights to indicate you are making a change to adult/ped NIBP limits or inflation pressure settings. 26.
Equipment overview: Rear panel 1. External DC power socket: used with approved GE AC-DC power converter only. Refer to “Parts lists and drawings” on page 6-1 for the part number of the approved power supply. Rear panel 3 2 2. Host communication port (15 pin D-type) for use only with equipment conforming to IEC 60601-1 or configured to comply with IEC 60601-1-1. The Exergen scanner connects to this port. NOTES 3. For connection details, see “Host communication connector” on page 315.
Equipment overview: Product compliance development of applications exchanging data with the CARESCAPE V100 vital signs monitor. An interface to the Pyxis Nursing Data Collection mobile clinical data collection application from CareFusion Corporation. Remote Alarm Cable: This cable connects the CARESCAPE V100 vital signs monitor to the hospital’s remote alarm “Nurse Call” system to provide remote alarming. For more information, see “Host communication connector” on page 3-15.
Equipment overview: Overall principles of operation The monitor is a portable unit that receives power from an internal rechargeable lead-acid main 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 main battery. The external DC source is used only to charge the main battery. Once the monitor is energized, a self-test is performed.
Equipment overview: Overall principles of operation has one valve, which is used to deflate the cuff. Valve control is through the Main Board. When the cuff pressure data acquisition for the determination is complete, the processor on the Main Board calculates the systolic NIBP, the diastolic NIBP, the Mean Arterial Pressure (MAP), and the pulse rate. The results are then displayed on the UI Board and sent to the printer (if the user presses the Print button).
Equipment overview: Overall principles of operation Full NIBP determination sequence for adult (specific pressure values are examples only) At each step the microprocessor stores cuff pressure, the matched pulse amplitude, and the time between successive pulses. The stepped deflation and matched pulse detection continues until diastolic pressure is determined or total cuff pressure falls below 8 mmHg.
Equipment overview: Overall principles of operation The SuperSTAT algorithm evaluates the data obtained during the determination, and the prior determination if it is available, to determine if additional data is needed to complete the determination. It can then selectively pump to a single cuff pressure to obtain the data it needs and then return to the existing deflation sequence. This search process makes SuperSTAT more efficient.
Equipment overview: Overall principles of operation cuff pressure falls below 7 mmHg. The monitor then deflates the cuff (to zero detected pressure), analyzes the stored data, and updates the screen. The operating cycle is composed of four parts: inflation time, deflation time, evaluation time, and wait time. Wait time, which varies from mode to mode, is affected by the cycle time (auto mode) or operator intervention (manual mode). The figure shows the basic operating cycle.
Equipment overview: Overall principles of operation Monitors with auscultatory reference (DINAMAP auscultatory reference technology) In these monitors, the reference blood pressure is the auscultatory method for adult and pediatric populations. For neonatal populations, the usual reference is the invasive blood pressure obtained from the umbilical artery. NOTE For neonatal determinations the SuperSTAT algorithm is always used.
Equipment overview: Functional description temperature measurement, but not a fast (predictive) axillary temperature measurement. The Tri-Site temperature option can take a fast (predictive) oral, rectal, or axillary measurement. Both the Turbo Temp and Tri-Site temperature options can take a continuous (monitor) oral, rectal, or axillary measurement.
Equipment overview: Functional description Independent software in the primary and secondary processor periodically communicates 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.
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.
2048723-002D CARESCAPE V100 Vital Signs Monitor 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 des
Equipment overview: Functional description For your notes 2-18 CARESCAPE V100 Vital Signs Monitor 2048723-002D
3 2048723-002D Installation CARESCAPE V100 Vital Signs Monitor 3-1
Installation: Unpacking and preparation for installation Unpacking and preparation for installation 1. Unpack and identify the contents of all shipping materials. 2. Remove the monitor. 3. Unpack the AC cord. 4. Plug the AC cord into the AC Mains input on the external power supply, and plug the supply DC output into the side of the monitor. NOTE Use only the original cord, a power cord recommended by GE, or a regulatory-approved cord for the country of use. 5.
Installation: Powering the monitor Charge battery pack for 8 hours before first use or after prolonged periods of storage. If the monitor is idle for extended periods, it should be fully charged at least once a month to ensure optimum performance. If the monitor is to be stored for longer than one month, first charge the battery and then remove it and store it separately from the monitor. The battery pack should be charged before use, because a charged battery loses charge when left in storage.
Installation: Powering the monitor When about 5 minutes of main battery charge remains: The low-priority BATTERY LOW alarm escalates to a high-priority BATTERY LOW alarm. The BATTERY LOW indicator flashes. Any NIBP determination in progress at the time of the alarm escalation is allowed to finish. Any Stat mode cycle that was initiated before the alarm escalation is allowed to finish.
Installation: Configuring the monitor Configuring the monitor Operating modes The 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 the monitor Display Window Major software revision Systolic Minor software revision Diastolic Type of NIBP technology min Temperature type technology Temperature These displays appear only during the first part of the power up sequence and are not selectable and cannot be changed. After a moment, this version information is cleared, and the monitor displays the first page of configuration mode which simply displays in the Systolic window.
Installation: Configuring the monitor Setting Pulse Rate window display Window LED display SpO2 sat (Masimo only) SpO2 0 or 1 Fast Sat Mode 0=Off 1=On* SpO2 sensitivity (Masimo only) SpO2 1, 2, 3 1= Low Perfusion-Maximized, 2= Low Perfusion-Default, 3= for engaging Adaptive Probe Off Technology algorithm* Temperature units Temperature blank C or F indicator illuminated (Alaris only) Temperature display time Temperature 2 or 5 User selects number of minutes temperature values are displaye
Installation: Configuring the monitor and select the parameter function. To change alarm settings, press the Alarms button. 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. 2. Use the +/- buttons to increment or decrement the inflate pressure default setting. 3. To exit the configuration mode, turn the unit off.
Installation: Configuring the monitor NOTE For monitors configured for Ohmeda TruSignal SpO2 only, verify that the setting for Line Frequency mode (LF) is correct for your country. Refer to “SpO2 configuration settings” on page 3-9. SpO2 configuration settings Procedure for units with Ohmeda TruSignal technology 1. With the monitor off, press and hold the Menu button at the same time as pressing the On/Off button until the display test completes. 2.
Installation: Configuring the monitor 6. Press the Menu button once. SEn (sensitivity mode) appears in the Pulse Rate window. 7. Use the +/-buttons to select the option. 8. To exit the configuration mode, turn the unit off. To continue with additional configuration settings, press the Menu button. Temperature unit of measurement configuration settings Procedure for units with Alaris probes 1.
Installation: Configuring the monitor 3. To set the unit of measurement to: °F — move the switch up toward the probe cone °C — move the switch away from the probe cone °F F/C switch °C 4. Replace the cover, and tighten the screw. Temperature display time configuration settings User selects number of minutes temperature values are displayed. NOTE This procedure applies to both the Alaris probe and the Exergen scanner. 1.
Installation: Configuring the monitor You can then press the Menu button to cycle through all the advanced configuration mode option pages. After all options pages have been displayed, the display will return to the first advanced configuration mode page (displaying ACF). You can use the + and - buttons to make changes to settings. After making changes, simply cycle the power to return to normal operation mode. Changes are automatically be retained.
Installation: Configuring the monitor NOTE The first tone sounds as you first press the Menu button and the second tone sounds after the monitor has saved the settings. After all options pages have been displayed, the display will return to the first service mode page (initial calibration page). The Service Mode option pages are as follows: Displayed on monitor Function 0 (in min window) Refer to calibration section for functions. 1 (in min window) Refer to calibration section for functions.
Installation: Configuring the monitor Displayed on monitor Function 5 (in min window) Temperature loaded (Displayed in Temperature display window) 0: No Temp 1: Alaris Turbo Temp 2: Alaris Tri-Site 3: Exergen 6 (in min window) Language 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. Russian, Greek, Korean, and Japanese are printed in English only.
Installation: Host communication connector Host communication connector CAUTION Auxiliary equipment connected to the CARESCAPE V100 vital signs monitor will result in the formation of an electromedical system and thus, must comply with the requirements of IEC 60601-1-1. All host port signals are NON-ISOLATED and should be connected to equipment conforming to IEC-60601-1 or configured to comply with IEC 60601-1-1 only.
Installation: Host communication connector DB15 connector pin assignments Connection details Host port connector (rear panel) Pin # Function 1 Common 2 Inverted TTL Transmit Data 3 Inverted TTL Receive Data 4 +5 volts 5 No connection 6 No connection 7 Common 8 Remote Alarm 9 No connection 10 No connection 11 RS232 Transmit Data (TxD) 12 No connection 13 RS232 Receive Data (RxD) 14 No connection 15 No connection Communication protocol GE offers resources to assist customers
4 2048723-002D Maintenance CARESCAPE V100 Vital Signs Monitor 4-1
Maintenance: Preventative maintenance Preventative maintenance WARNING Failure on the part of all responsible individual, hospital, or institution using this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards. WARNING Calibration equipment should always be kept dry and free of particulate matter.
Maintenance: Visual inspection Visual inspection The monitor and its components should be carefully inspected prior to installation, once every 12 months thereafter and each time the equipment is serviced. WARNING Do not use damaged sensors, cables, or connectors. Carefully inspect the equipment for physical damage to the case, the display screen, and the keypad. Do not use the monitor if damage is determined. Refer damaged equipment to qualified service personnel.
Maintenance: Cleaning Cleaning the exterior surfaces of the monitor, monitor accessories, or the Exergen temporal scanner Disconnect the monitor from AC power before cleaning or disinfecting its surface. The exterior surfaces of the monitor, monitor accessories, and temporal scanner may be cleaned with a dampened, lint-free cloth. Wipe off all cleaning solutions with a clean, dry cloth and let air dry for at least 15 minutes.
Maintenance: Cleaning Cleaning and disinfecting blood pressure cuffs General The cuff must be thoroughly cleaned with the specified detergent before reuse. The additional use of household bleach as described below provides at least intermediate-level disinfection. NOTE Never autoclave or steam clean the monitor, cuffs, or accessories. Apply cuff hose caps before cleaning. See “NIBP accessories” on page 6-2 for the orderable part numbers of cuff hose caps.
Maintenance: Long-term storage Cleaning the exterior surfaces of the Alaris temperature devices It is good practice to periodically clean the probe’s surface by wiping it with a soft cloth dampened with a mild detergent and warm water. Refer to the Housekeeping, Central Service or Infection Control departments in your facility for further information. You may use the following cleaning solutions: Cidex®, Betadine®, or 3% hydrogen peroxide. NOTE Betadine may discolor the case.
Maintenance: Long-term storage Long-term storage at high temperatures can lead to deterioration of seals and separators and should be avoided. Battery care Main battery WARNING Keep the monitor connected to an external DC power source when not in use to ensure maximum battery charge. NOTE The expected lifetime of the battery largely depends on the way in which the monitor is used. If the battery is allowed to discharge to 50%, it should survive approximately 400 charge/discharge cycles.
Maintenance: Long-term storage Battery charging will take place as long as the monitor remains connected to an external DC power source. Replacing the main battery on the monitor DANGER Before replacing the battery, disconnect the monitor from the DC power supply. NOTES Record the configuration settings on your monitor before replacing the battery. When the battery is replaced, all user settings are lost and return to default values. Replacement batteries can be obtained from GE. 1.
Maintenance: Long-term storage 6. Insert the battery into the compartment. 7. Replace the cover, help card tray, and screws. Insert the external DC power converter plug into the external DC power socket and plug into an AC outlet. NOTES Error code ‘E00’ appears (MEMORY LOST) alerting you that the user settings (including alarm limits and inflation pressure) and date/time will go back to default values and all entries in clinical history are erased.
Maintenance: Long-term storage 2. Loosen the single screw at the bottom, on the back of the scanner, and remove the battery cover. Cover 9-volt battery Single screw 3. Disconnect the old battery and replace with a new, high quality 9-volt alkaline battery in the same location. 4. Replace the battery cover, and tighten the screw. 5. Reconnect the scanner cable to the host communication port, and tighten the two thumbscrews. Fuses The monitor contains three fuses.
Maintenance: Parameter level functional testing Parameter level functional testing Use the accessories supplied with the monitor to perform functional testing of each of the parameters after the initial configuration is complete. Refer to the operator’s manual for more detailed parameter-specific instructions. NIBP 1. Perform an NIBP determination on yourself. a. Connect the supplied air hose and cuff together. b. Connect the end of the air hose to the NIBP connector on the front of the monitor. c.
Maintenance: Parameter level functional testing Exergen 1. Connect the Exergen temporal scanner’s modular plug to the host communication port at the back of the monitor. 2. Take a temperature reading of yourself (i.e., not on a resistor simulator). 3. Verify that the temperature displays both on the Exergen temporal scanner and in the Temperature window on the monitor.
Maintenance: Calibration procedures and tests Calibration procedures and tests Perform the following calibration test procedures every 12 months, or whenever the accuracy of any reading is in doubt. NOTE All devices are tested and calibrated during manufacturing and are certified for operation at installation.
Maintenance: Calibration procedures and tests Setup 1. Connect manometer to unit as shown. 2. ‘T’ an inflation bulb into the pneumatic setup. 3. Consult the following diagram for pneumatic setup guidelines. NIBP tests Pneumatic leakage testing NOTE To enter Service Mode press and hold the Cycle button while pressing the On/Off button. 4-14 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.
Maintenance: Calibration procedures and tests The leakage rate is the difference between the first and second readings. 8. Record and verify the leakage rate on the “Test results form” on page 4-29. 9. Turn the monitor off. 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.
Maintenance: Calibration procedures and tests Pressure transducer calibration Perform only if Pressure Transducer Verification is out of tolerance as specified in the “Test results form” on page 4-29. NOTE To enter service mode press and hold Cycle button while pressing the On/ Off button. 1. Turn the 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. Verify the manometer reads zero. 5.
Maintenance: Calibration procedures and tests Button testing 1. Disconnect the cuff/hose assembly and power on the unit. 2. Press Inflate/Stop button. 3. Verify a NIBP determination has been initiated. 4. Block pump port and verify ‘E80’ alarm. 5. Press Silence button, verify alarm has been cleared. 6. Verify that the alarm silence indicator (bell) is lit. 7. Press Alarm button several times, verify unit cycles through all alarm settings (i.e., SYS, DIA, SpO2). 8.
Maintenance: Calibration procedures and tests 7. Press the Silence button again. 8. Verify the alarm condition is cleared from the Systolic window. 9. Confirm all test results are recorded on the “Test results form” on page 4-29. 1. Power on the monitor. 2. During the power-up self-test verify all 7 segment LEDs and all discrete LEDs illuminate and they are the correct color.
Maintenance: Calibration procedures and tests Alaris temperature calibration verification NOTES There are no user-performed maintenance or calibration procedures for Alaris thermometry. To verify the accuracy of the Alaris temperature parameter with a specific temperature probe, take measurements at varying temperatures in continuous (monitor) mode using a water bath and a high-precision thermometer as a reference instrument. 1. Turn the monitor off.
Maintenance: Calibration procedures and tests Alaris temperature probe date of manufacture If required for your maintenance procedures, the Alaris temperature probe’s date of manufacture is stamped into the probe’s RJ45 connector. The first two digits equal the year of manufacture, the second two digits equal the week of manufacture. In the example below, 0835 equals fiscal week 35 in the year of 2008.
Maintenance: Calibration procedures and tests 1. Turn on the verifier device, using either a 9-volt battery or the power supply. Make sure the red LED is illuminated. Power On LED On/Off switch Battery compartment Power supply jack 2. Allow device approximately 5 minutes for warm-up and stabilization time. 3. Allow certified master and the instrument to be tested to acclimate in the same ambient temperature for at least 10 minutes. 4.
Maintenance: Calibration procedures and tests 3. Remove the sensor from your finger to generate a ‘---’ (SpO2 SENSOR OFF FINGER) alarm and to sound the speaker. 4. Press the Silence button. 5. Verify the sound has stopped and the ‘---’ (SpO2 SENSOR OFF FINGER) error is cleared. 6. Re-apply the SpO2 sensor to your finger. 7. Verify the unit displays a: Pulse value Saturation value Signal Strength Bar Graph 8. Confirm all test results are recorded on the “Test results form” on page 4-29.
Maintenance: Safety testing 2. Firmly press the door to close it. 3. Press Print button. 4. Verify the printer outputs a record and print quality is good. 5. Confirm test results are recorded on the “Test results form” on page 4-29. Safety testing Electrical safety tests Electrical safety tests provide a method of determining if potential electrical health hazards to the patient or operator of the device exist.
Maintenance: Safety testing Test equipment The recommended test equipment required to perform electrical safety tests is listed below. Item Specification Leakage Current Tester Equivalent to the circuits shown Digital Multimeter (DMM) (optional, based upon leakage tester and location) AC volts, ohms SpO2 Test Body 2006036-001 Safety Testing Cable Kit 2026107-006 NOTE This kit contains the Temperature Test Body.
Maintenance: Safety testing Patient leakage current test This procedure measures the leakage current from the “Device Under Test” input connector to ground. Perform tests in both Normal Condition (NC) and in Single Fault Condition (SFC), where one of the supply conductors is open at a time. Perform the test with normal and reverse polarity. NOTE *The MD represents the network and voltage measuring instrument and its frequency characteristics per IEC 60601-1.
Maintenance: Safety testing 6. Read the current leakage indicated on the tester and record the results on the “Test results form” on page 4-29. 7. Change leakage tester switches to: Polarity – NORMAL Neutral – CLOSED GND (Earth) – OPEN 8. Read the current leakage indicated on the tester and record the results on the “Test results form” on page 4-29. 9. Change leakage tester switches to: Polarity – REVERSED Neutral – CLOSED GND (Earth) – OPEN 10.
Maintenance: Safety testing Patient leakage current test (mains voltage on the applied part) This procedure measures the leakage current from a mains voltage source into the “Device Under Test” input connector. The patient connector test body shorts all signals in the connector together. Refer to the instructions contained with the safety analyzer to perform this test. Connect the appropriate Test Body to the input connector of the device under test. Perform the test with normal and reverse polarity.
Maintenance: Safety testing 4. Change leakage tester switches to: Polarity – REVERSED Neutral – CLOSED GND (Earth) – CLOSED 5. Read the current leakage indicated on the tester and record the results on the “Test results form” on page 4-29. 6. Remove the AC mains voltage from the device under test. 7. Repeat the steps in this procedure using the appropriate Test Body for any additional patient connectors requiring safety testing.
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.
Maintenance: Test results form Description Min Max Rev Pol, Neut Open, Gnd Clsd 500µA Rev Pol, Neut Clsd, Gnd Clsd 100µA Actual Pass-Fail-N/A Patient leakage current (mains on applied part) 2048723-002D Fwd Pol, Neut Clsd, Gnd Clsd 5mA Rev Pol, Neut Clsd, Gnd Clsd 5mA CARESCAPE V100 Vital Signs Monitor 4-31
Maintenance: Test results form 4-32 CARESCAPE V100 Vital Signs Monitor 2048723-002D
5 2048723-002D Troubleshooting CARESCAPE V100 Vital Signs Monitor 5-1
Troubleshooting: Overview Overview The symptoms and solutions in this chapter represent only a few of the problems that you may encounter and are not intended to cover every possible problem that may occur. A systematic approach to the diagnosis of problems as well as a general understanding of the architecture, both hardware and software, of the monitor are essential to ensure successful troubleshooting of a device. GE recommends formal service training before repairs are attempted.
Troubleshooting: Alarm code interpretation Alarm code interpretation General system error codes are listed in this section. If any other system or similar code appears, record the error message and report the failure to GE Technical Support. Refer to the operator’s manual for information about patient alarms and general procedural alarms. System failures System failure mode is entered when the monitor has a depleted battery, or a hardware or software failure.
Troubleshooting: Alarm code interpretation 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.
Troubleshooting: Alarm code interpretation Can be acknowledged (silenced)?* Error code or problem Source 976 System Power supply voltage has peaked above 18 Volts (incorrect power supply) No External power brick issue 979 System Unknown power processor mode received on power-up No Mains PWA issue 980 System Heap memory exhausted No Mains PWA issue 984 System Unused vector called No Return unit for evaluation 985 System RTK 400hz timer re-entry No Return unit for evaluation 986
Troubleshooting: Alarm code interpretation Can be acknowledged (silenced)?* Probable source Temp probe broken (Alaris only) No Replace temperature probe Temp Temp probe disconnected (Alaris only) Yes Check for correct probe E66 Temp Temp probe too hot (Alaris only) Yes Replace probe E-- Temp Temp scanner error (Exergen only) Yes Check Exergen battery, and check for valid temperature value. Also check the scanner’s display for Exergen error information.
Troubleshooting: Alarm code interpretation Exergen-specific error codes If the scanner is unable to take a temperature determination, or has a low battery, the monitor will display the ‘E--’ error code and generate an audible alarm. The scanner may also display additional indicators on the LED display.
Troubleshooting: Alarm code interpretation For your notes 5-8 CARESCAPE V100 Vital Signs Monitor 2048723-002D
6 2048723-002D Parts lists and drawings CARESCAPE V100 Vital Signs Monitor 6-1
Parts lists and drawings: Ordering parts Ordering parts This section of the manual provides parts lists for the 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 fieldinstalled upgrades, the revision level of a diagram or parts list in this manual may not reflect the revision level of your unit’s subassemblies.
Parts lists and drawings: Compatible service parts Part Part description Part number NIBP, Cuff, Soft Cuff, Infant SOFT-CUF, Infant, 2 TB, Screw, Orange/White 8 - 13 cm 2500 NIBP, Cuff, Soft Cuff, Child SOFT-CUF, Child, 2 TB, Screw, Green/White 12 - 19 cm 2501 NIBP, Cuff, Soft Cuff, Child Long SOFT-CUF, Child Long, 2 TB, Screw, Green/White 12 - 19 cm 2506 NIBP, Cuff, Soft Cuff, Sm Adult SOFT-CUF, Small Adult, 2 TB, Screw, Lt.
Parts lists and drawings: Compatible service parts Part NIBP, Cuff, Classic Cuff, Lg Adult Long Part description CLASSIC-CUF, Large Adult Long, 2 TB, Mated Submin, Rose/White 31 40 cm Part number 2176 NIBP, Cuff, Classic Cuff, Thigh CLASSIC-CUF, Thigh, 2 TB, Mated Submin, Brown/White 38 - 50 cm 2177 NIBP, Cuff, Classic Cuff, Infant 2354 CLASSIC-CUF, Infant, 2 TB, Submin, Orange/White 8 - 13 cm NIBP, Cuff, Classic Cuff, Child CLASSIC-CUF, Child, 2 TB, Submin, Green/White 12 - 19 cm 2355 NIBP, Cuff
Parts lists and drawings: Compatible service parts Part Part description Part number NIBP, Cuff, Classic Cuff, Thigh CLASSIC-CUF, Thigh, 2 TB, Submin, Yellow 38 - 50 cm 2675 NIBP, Cuff, Classic Cuff, Infant CLASSIC-CUF, Infant, 2 TB, Submin, Yellow 8 - 13 cm 2650 NIBP, Cuff, Classic Cuff, Child CLASSIC-CUF, Child, 2 TB, Submin, Yellow 12 - 19 cm 2651 NIBP, Cuff, Classic Cuff, Sm Adult 2607 CLASSIC-CUF, Small Adult, 2 TB, Submin, Yellow 17 - 25 cm NIBP, Cuff, Classic Cuff, Adult CLASSIC-CUF, Ad
Parts lists and drawings: Compatible service parts Part Part description Part number NIBP, Cuff, Sensa Cuff, Sm Adult Long SENSA-CUF, Small Adult Long, 2 TB, Submin, Royal Blue 17 - 25 cm 2487 NIBP, Cuff, Sensa Cuff, Adult SENSA-CUF, Adult, 2 TB, Submin, Navy 23 - 33 cm 2488 NIBP, Cuff, Sensa Cuff, Adult Long SENSA-CUF, Adult Long, 2 TB, Submin, Navy 23 - 33 cm 2489 NIBP, Cuff, Sensa Cuff, Lg Adult SENSA-CUF, Large Adult, 2 TB, Submin, Wine 31 - 40 cm 2490 NIBP, Cuff, Sensa Cuff, Lg Adult Lo
Parts lists and drawings: Compatible service parts Part Part description Part number NIBP, Cuff, Dura Cuff, Adult DURA-CUF, Adult, 2 TB, Mated Submin, Navy 23 - 33 cm 2753E NIBP, Cuff, Dura Cuff, Adult Long DURA-CUF, Adult Long, 2 TB, Mated Submin, Navy 23 - 33 cm 002756E NIBP, Cuff, Dura Cuff, Lg Adult DURA-CUF, Large Adult, 2 TB, Mated Submin, Wine 31 - 40 cm 2754E NIBP, Cuff, Dura Cuff, Lg Adult Long DURA-CUF, Large Adult Long, 2 TB, Mated Submin, Wine 31 - 40 cm 002757E NIBP, Cuff, Dura
Parts lists and drawings: Compatible service parts Part Part description Part number NIBP, Cuff, Dura Cuff, Various DURA-CUF, Assortment, 2 TB, Submin: 1 Infant, 1 Child, 1 Small Adult, 1 Adult, 1 Large Adult, 1 Thigh, Various limb circum 2299 NIBP, Cuff, Dura Cuff, Various DURA-CUF, Assortment, 2 TB, Screw: 1 Infant, 1 Child, 1 Small Adult, 1 Adult, 1 Large Adult, 1 Thigh, Various limb circum 002699 NIBP, Cuff, Dura Cuff, Child DURA-CUF, Child Assortment, 2 TB, Screw: 2 Infant, 3 Child, 1 Small Ad
Parts lists and drawings: Compatible service parts SpO2 - Ohmeda accessories Part Part description Part number SpO2 - Cable Assy TruSignal Interconnect cable with GE connector TS-G3 SpO2 - Sensor TruSignal Finger Sensor with integrated cable, 2 m TS-F2-GE SpO2 - Sensor TruSignal Finger Sensor with integrated cable, 4 m TS-F4-GE SpO2 - Sensor TruSignal Finger Sensor TS-F-D SpO2 - Sensor TruSignal Soft Adult Sensor with integrated cable and D connector, 1 m TS-SA-D SpO2 - Sensor TruSignal
Parts lists and drawings: Compatible service parts SpO2 - Nellcor accessories Part Part description Part number SpO2 Cable Assy 3 m Cable Assy SpO2 Nellcor OxiMax 3 m - Smart 2021406-001 SpO2 Cable Assy 3 m Cable Assy SpO2 Nellcor OxiMax 1.
Parts lists and drawings: Compatible service parts Part Part description Part number SpO2 - Sensor Masimo LNOP Disposable Adhesive Sensor, LNOP-Neo-L. Neonatal - 20/box 2017089-001 SpO2 - Sensor Masimo LNOP Disposable Adhesive Sensor, LNOP NeoPTL.
Parts lists and drawings: Compatible service parts Part Part description Part number SpO2 - Accessory Masimo Tape Bag for LNOP-NEO - 100/box 2010467-001 SpO2 - Accessory Masimo Tape Cleanshield Multisite, LNOP-YI - 100/box 2010468-001 SpO2 - Accessory Masimo Disposable Standard Multisite Wrap, Adult/Ped/ Neonatal Adhesive Attachment Wraps, use with LNOP-YI Multisite Reusable Sensor - 100/box 2010469-001 SpO2 - Accessory Masimo Tape Standard Petite Wrap, LNOP-YI - 100/box 2010470-001 SpO2 - A
Parts lists and drawings: Compatible service parts Part Part description Part number Cable - Exergen Cable, Exergen TAT-5000 to V100 interface 2044860-005 Calibration - Exergen, Fahrenheit arterial Exergen calibration verification kit for °F calibrated to an arterial reference EX129003 Exergen Scanner Holder Exergen TAT-5000 holder and installation instructions 2051186-001 Power accessories Part Part description Part number Battery - CARESCAPE V100 vital signs monitor FRU CARESCAPE V100 vit
Parts lists and drawings: Compatible service parts Mounting accessories Part Part description Part number Roll Stand Rollstand, CARESCAPE, GCX Version 2033297-001 Pole Mount Pole Mount 2009762-001 Power Supply Mounting Bracket 12W Power supply roll stand bracket 2047870-001 Wall Mount Bracket GCX wall mount bracket for DP100 - 400 monitors CR-0008-01 IR adapter cable roll mount bracket IR adapter cable roll mount bracket 2025344-001 Connectivity accessories Part Part description Part nu
Parts lists and drawings: Field-replaceable units (FRUs) Field-replaceable units (FRUs) NOTE GE supports troubleshooting and repair to the FRU-level only. GE does not make available schematics, assembly drawings, or bills of material beyond what is provided in this manual. Attempting repair on a PCB or factorysealed component is not recommended.
Parts lists and drawings: Field-replaceable units (FRUs) Bubble Number Part Number 19f 2037103-066 FRU CARESCAPE V100 Fascia Kit - Dutch 19f 2037103-067 FRU CARESCAPE V100 Fascia Kit - Finnish 19f 2037103-068 FRU CARESCAPE V100 Fascia Kit - French 19f 2037103-069 FRU CARESCAPE V100 Fascia Kit - Greek 19f 2037103-070 FRU CARESCAPE V100 Fascia Kit - Hungarian 19f 2037103-071 FRU CARESCAPE V100 Fascia Kit - Italian 19f 2037103-072 FRU CARESCAPE V100 Fascia Kit - Japanese 19f 2037103-07
Parts lists and drawings: Field-replaceable units (FRUs) a Bubble Number Part Number 54a, j 2037103-086 Description FRU CARESCAPE V100 BZL, (BP & SpO2 & TEMP) MS-2011 All SpO2 technology labels included. Select applicable label per monitor configuration. b Main boards configured with SuperSTAT NIBP algorithm, Nellcor SpO2, and Temperature enabled. Reconfigure as applicable per monitor configuration. Refer to “Installation” Chapter 3 for more details. c All UI board LEDs installed.
Parts lists and drawings: Field-replaceable units (FRUs) FRU 2037103-004: CARESCAPE V100 temperature kit (Alaris) 6-18 CARESCAPE V100 Vital Signs Monitor 2048723-002D
Parts lists and drawings: Field-replaceable units (FRUs) FRU 2037103-005: CARESCAPE V100 printer assembly FRU 2037103-006: CARESCAPE V100 BZL, (BP only) FRU 2037103-052: CARESCAPE V100 BZL, (BP & Temp) FRU 2037103-053: CARESCAPE V100 BZL, (BP & SpO2) FRU 2037103-054: CARESCAPE V100 BZL, (BP & SpO2 & Temp) NOTE Kit includes only 1 bezel.
Parts lists and drawings: Field-replaceable units (FRUs) FRU 2037103-007: CARESCAPE V100 inner chassis kit NOTE Kit includes 4 adhesive-backed feet. FRU 2037103-008: CARESCAPE V100 Prtr door X1/rollers X5 NOTE Kit includes 1 printer door with label and 5 printer rollers.
Parts lists and drawings: Field-replaceable units (FRUs) FRU 2037103-083: CARESCAPE V100 V1.5 main board NOTE Each main board comes with all parameters installed. For monitors that do not include specific options (Printer, SpO2, Temperature), these options must be turned off while the monitor is in configuration mode. Each main board comes configured with the SuperSTAT NIBP algorithm.
Parts lists and drawings: Field-replaceable units (FRUs) Masimo (MS-11) Masimo (MS-2011) Nellcor Ohmeda FRU 2037103-013: CARESCAPE V100 SpO2 Nellcor FRU 2037103-023: CARESCAPE V100 SpO2 Masimo or FRU 2037103-084 CARESCAPE V100 SpO2 Masimo MS-2011 FRU 2037103-024: CARESCAPE V100 SpO2 Ohmeda NOTE All 4 SpO2 boards shown. Kit includes only one. Nellcor hardware shown. Kit includes matching hardware.
Parts lists and drawings: Field-replaceable units (FRUs) FRU 2037103-016: CARESCAPE V100 main battery (X1 BATT) FRU 2037103-017: CARESCAPE V100 speaker 2048723-002D CARESCAPE V100 Vital Signs Monitor 6-23
Parts lists and drawings: Field-replaceable units (FRUs) FRU 2037103-018: CARESCAPE V100 cable kit FRU number 6-24 Description Language FRU 2037103-062 CARESCAPE V100 Fascia Kit English FRU 2037103-063 CARESCAPE V100 Fascia Kit German FRU 2037103-064 CARESCAPE V100 Fascia Kit Czech FRU 2037103-065 CARESCAPE V100 Fascia Kit Danish CARESCAPE V100 Vital Signs Monitor 2048723-002D
Parts lists and drawings: Field-replaceable units (FRUs) FRU number 2048723-002D Description Language FRU 2037103-066 CARESCAPE V100 Fascia Kit Dutch FRU 2037103-067 CARESCAPE V100 Fascia Kit Finnish FRU 2037103-068 CARESCAPE V100 Fascia Kit French FRU 2037103-069 CARESCAPE V100 Fascia Kit Greek FRU 2037103-070 CARESCAPE V100 Fascia Kit Hungarian FRU 2037103-071 CARESCAPE V100 Fascia Kit Italian FRU 2037103-072 CARESCAPE V100 Fascia Kit Japanese FRU 2037103-073 CARESCAPE V100 Fasc
Parts lists and drawings: Field-replaceable units (FRUs) 1 2 19 3 4 20 13 5 6 14 21 15 7 16 8 10 9 17 11 12 22 18 FRU 2037103-022: CARESCAPE V100 all hardware kit NOTE Each Hardware kit includes the following: Item 6-26 Description Torque specifications Qty 1 Cable Tie, Locking, Nylon 6.6, 3.1" X 0.09” 5 2 Tie Wrap Intermediate, 2” 10 3 Screw, Mach Pnhd 832 X 2-1/2 SS Vibratite 8 in-lb ± 0.5 in-lb 6 4 Screw, No6, Torx Pan, 1.0 Inch Vib 8 in-lb ± 0.
Parts lists and drawings: Field-replaceable units (FRUs) Item Description Torque specifications Qty 16 Tubing Silicone 1/8 ID X 1/4 OD 1 foot 17 Tubing Silicone Clear 3/32” ID 7/32” OD 1 foot 18 Conn Plastic Tee 4 19 Speaker Clamp Ring 3 20 Adhesive Backed Cable Tie Mount, 0.75 X 0.75 5 21 Extrusion Grommet, handle 3 22 Filter 40 Micron 10 FRU 2037103-044: CARESCAPE V100 keypad kit NOTE Printer version shown.
Parts lists and drawings: Field-replaceable units (FRUs) FRU main reference guide drawing For quick reference use the following FRU main reference guide drawing.
Parts lists and drawings: Field-replaceable units (FRUs) 2048723-002D CARESCAPE V100 Vital Signs Monitor 6-29
Parts lists and drawings: Field-replaceable units (FRUs) 6-30 CARESCAPE V100 Vital Signs Monitor 2048723-002D
Parts lists and drawings: Field-replaceable units (FRUs) 2048723-002D CARESCAPE V100 Vital Signs Monitor 6-31
Parts lists and drawings: Field-replaceable units (FRUs) 6-32 CARESCAPE V100 Vital Signs Monitor 2048723-002D
Parts lists and drawings: Field-replaceable units (FRUs) 2048723-002D CARESCAPE V100 Vital Signs Monitor 6-33
Parts lists and drawings: Field-replaceable units (FRUs) 6-34 CARESCAPE V100 Vital Signs Monitor 2048723-002D
Parts lists and drawings: Field-replaceable units (FRUs) 2048723-002D CARESCAPE V100 Vital Signs Monitor 6-35
Parts lists and drawings: Disassembly/reassembly of FRUs Disassembly/reassembly of FRUs Electrostatic discharge (ESD) precautions All external connectors of the monitor are designed with protection from ESD damage. However if the monitor requires service, exposed components and assemblies inside are susceptible to ESD damage. This includes human hands, non-ESD protected work stations or improperly grounded test equipment.
Parts lists and drawings: Disassembly/reassembly of FRUs Monitor fascia replacement procedure 2048723-002D 1. Pry open the front face plate at the upper corners and remove the face plate. 2. Remove the existing fascia. 3. Remove the tab at the top of the new fascia that includes the part number.
Parts lists and drawings: Disassembly/reassembly of FRUs 6-38 4. Turn the fascia over and remove the protective liner from the three pieces of double-sided adhesive tape. 5. Turn the fascia right side up and align the fascia with the bottom notch on the monitor. 6. Press the fascia onto the monitor. 7. Tuck the top part of the fascia under the top notch on the monitor.
Parts lists and drawings: Disassembly/reassembly of FRUs 8. Place the tabs on the bottom edge of the face plate into the slots on the monitor. 9. Snap the face plate back on the monitor. Monitor disassembly procedure The following procedure is sequential (i.e., you must remove the main battery and rear case to remove the printer, etc.). CAUTION Internal electronic components are susceptible to damage by electrostatic discharge.
Parts lists and drawings: Disassembly/reassembly of FRUs 3. The battery can now be removed. 1. Remove remaining two screws from the bottom of the monitor. 2. Set monitor upright. 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.
Parts lists and drawings: Disassembly/reassembly of FRUs 7. Unplug speaker cable and temperature module cable (if installed) from circuit board. 1. Lift the 2 black tabs and remove printer cable. 2. Remove printer assembly. 3. Unplug air hose from valve and filter. 4. Remove remaining 3 cable assemblies. 5. Locate and release retention tab and slide back sub chassis.
Parts lists and drawings: Disassembly/reassembly of FRUs 6. Remove sub-chassis and set aside. 7. Remove pneumatic assembly from sub-chassis. 1. Remove 2 screws securing SpO2 board. SpO2 board Threaded standoffs have screws on both ends. 2. Remove SpO2 board. 1. Remove 2 SpO2 connector screws. 2. Unplug 2 pneumatic hoses from bezel. 3. Remove 4 torx-head screws along the bottom of main board. 4. Lift unit and remove bezel.
Parts lists and drawings: Disassembly/reassembly of FRUs Main board 1. Remove 9 torx-head screws. 1. Carefully lift the Main board away from the UI board. 2. Collect the 5 spacers used to align the Main and UI board. 3. Lift the UI 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 lists and drawings: Disassembly/reassembly of FRUs review all material included in your kit. Exergen TAT Cable replacement 6-44 1. Turn off the monitor and unplug the cable from the host communication port on the back of the monitor. 2. On the back of the scanner, loosen the single screw at the bottom. 3. Remove the battery door. 4. Remove the cable. 5. Install the replacement cable.
Parts lists and drawings: Disassembly/reassembly of FRUs 7. 2048723-002D Screw the cable connector jack to the host communication port on the back of the monitor.
Parts lists and drawings: Disassembly/reassembly of FRUs For your notes 6-46 CARESCAPE V100 Vital Signs Monitor 2048723-002D
A 2048723-002D Technical specifications and default settings CARESCAPE V100 Vital Signs Monitor A-1
Technical specifications and default settings: Specifications Specifications General General specifications Mechanical Dimensions Height 19.5 cm (7.7 in) Width 21.9 cm (8.6 in) without temperature 25.4 cm (10.0 in) with temperature Depth 13.5 cm (5.3 in) Weight (Including battery) 2.4 kg (5.
Technical specifications and default settings: Specifications General specifications Storage/transportation Storage temperature – 20°C to + 50°C (– 4°F to + 122°F) 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) for radiated and conducted emissions Printer Printer specifications Printer type Therma
Technical specifications and default settings: Specifications NIBP WARNING Use only GE CRITIKON blood pressure cuffs. The size, shape, and bladder characteristics can affect the performance of the instrument. Inaccurate readings may occur unless GE CRITIKON blood pressure cuffs are used.
Technical specifications and default settings: Specifications Ohmeda SpO2 Ohmeda SpO2 specifications Measurement range SpO2 1 to 100% Pulse rate 30 to 250 bpm Perfusion Index Value (Plr) 0.00 to 9.
Technical specifications and default settings: Specifications Specifications: Ohmeda sensor accuracy SpO2 range 70% to 100% Sensor model OxyTip++ TS-F-D ±2 digits without motion TS-E-D ±3 digits without motion TS-W-D ±2 digits without motion TS-SE-3 ±2 digits without motion TS-AF-10 ±2 digits without motion TS-AF-25 ±2 digits without motion TS-F4-GE ±2 digits without motion TS-F2-GE ±2 digits without motion TS-E4-GE ±3 digits without motion TS-E2-GE ±3 digits without motion Specificati
Technical specifications and default settings: Specifications Nellcor SpO2 WARNING Nellcor-labeled monitors are only compatible with Nellcor Oximax sensors and cables. Nellcor SpO2 specifications Measurement range SpO2 1 to 100% Pulse rate 20 to 250 bpm Perfusion range 0.
Technical specifications and default settings: Specifications Specifications: Nellcor sensor accuracy NOTE All Nellcor OXIMAX sensors must be used with the NELL cable; the SCP-10 cable. RS-10 and Oxisensor II sensors are not compatible with the CARESCAPE V100 vital signs monitor.
Technical specifications and default settings: Specifications Specifications: Nellcor sensor accuracy D-YS & D-YSE ± 3.5 digits D-YS & D-YSPD ± 3.
Technical specifications and default settings: Specifications Masimo SpO2 WARNING Use only Masimo oximetry sensor for SpO2 measurements. Other oxygen transducers (sensors) may cause improper SpO2 performance. WARNING Monitors identified as having Masimo SET technology are compatible only with Masimo SET sensors and cables. Masimo SpO2 specifications Measurement range SpO2 1 to 100% Pulse rate 25 to 240 bpm Perfusion range 0.
Technical specifications and default settings: Specifications Specifications: Masimo sensor accuracy SpO2 range 70% to 100% Sensor model LNOP LNOP ADT ± 2 digits without motion LNOP NEO ± 3 digits without motion LNOP NEO-L Foot Finger ± 3 digits without motion ± 2 digits without motion LNOP NEO PT-L ± 3 digits without motion LNOP Adtx ± 2 digits without motion LNOP Pdtx ± 2 digits without motion LNOP DCI ± 2 digits without motion LNOP DCIP ± 2 digits without motion LNOP Hi Fi-Neo/adult Foo
Technical specifications and default settings: Specifications Specifications: Masimo sensor accuracy LNCS DC-I ± 2 digits without motion LNCS DC-IP ± 2 digits without motion LNCS Adult Adtx ± 2 digits without motion LNCS Ped Pdtx ± 2 digits without motion LNCS Infant-L ± 2 digits without motion LNCS Neo PT-L ± 3 digits without motion Resolution Saturation (% SpO2) 1% Pulse rate (bpm) 1 Low perfusion performance 0.
Technical specifications and default settings: Specifications Temperature WARNING Alaris: Use only recommended probes and probe covers. The size, shape, and thermal characteristics of the probe covers can affect the performance of the instrument. Inaccurate readings may occur unless recommended probes and probe covers are used. Visually inspect the probe prior to use to be sure it is defect free. Please refer to the Accessories list provided with your monitor.
Technical specifications and default settings: Specifications Temperature specifications Exergen Measurement Mode Accuracy Max: 43°C; 110°F Min: 16°C; 61°F ±0.1°C; ±0.2°F meets EN 12470-5 Predictive Mode Not applicable Monitor Mode Not applicable Operating environment 16° to 40°C; 60° to 104°F (ambient) Arterial head balance range for body temperature* 34.5° to 43°C; 94° to 110°F Resolution 0.1°C or 0.1°F Response time approx. 0.
Technical specifications and default settings: Specifications Battery Monitor - main battery Battery specifications Capacity Battery life 6V; 3.3 Ahr sealed lead-acid battery 5 hours with SpO2 technology with a usage scenario of: NIBP determinations every 5 minutes with adult cuff Printout after every determination SpO2 parameter active at 60 bpm Temperature parameter active in monitor mode Up to 11.
Technical specifications and default settings: Default settings Default settings Alarms The factory default for alarm volume is 5.
Technical specifications and default settings: Default settings Nellcor SpO2 SpO2 (%) HIGH alarm limit 100 SpO2 (%) LOW alarm limit 90 Response mode 1 (for Mode 1: Normal response) SatSeconds 0 SpO2 (%) HIGH alarm limit 100 SpO2 (%) LOW alarm limit 90 Averaging time 12 seconds FastSAT mode 0 (for Off) Sensitivity mode 2 (for Low Perfusion) HIGH alarm limit 150 bpm LOW alarm limit 50 bpm Alarm volume 5 Unit of measure °F Temperature display time 2 minutes Masimo SpO2 Pulse rate
Technical specifications and default settings: Default settings Exergen A-18 Unit of measure °F or °C Defined by Exergen scanner purchased.
B 2048723-002D Appropriate use of NIBP simulators CARESCAPE V100 Vital Signs Monitor B-1
Appropriate use of NIBP simulators: Appropriate use of NIBP simulators Appropriate use of NIBP simulators NIBP accuracy Noninvasive Blood Pressure (NIBP) monitors are cleared 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 how an NIBP monitor analyzes the oscillometric envelope. While it is possible to 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 BioTek® NIBP Pump 2™ (Fluke Biomedical) manual, in response to the question of why monitor readings differ from the target values on the simulator, states: "Neither the monitor or the NIBP 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.
Appropriate use of NIBP simulators: Appropriate use of NIBP simulators Figure 2B: Cuff Oscillation From A Simulator Measurement References 2048723-002D 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.
Appropriate use of NIBP simulators: Appropriate use of NIBP simulators For your notes B-6 CARESCAPE V100 Vital Signs Monitor 2048723-002D
C 2048723-002D Electromagnetic compatibility (EMC) CARESCAPE V100 Vital Signs Monitor C-1
Electromagnetic compatibility (EMC): Electromagnetic compatibility (EMC): CARESCAPE V100 monitor Electromagnetic compatibility (EMC): CARESCAPE V100 monitor Changes or modifications to this system not expressly approved by GE Healthcare 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): CARESCAPE V100 monitor Guidance and manufacturer’s declaration – electromagnetic immunity The CARESCAPE V100 vital signs monitor is intended for use in the electromagnetic environment specified below. It is the responsibility of the customer or user to assure that the CARESCAPE V100 vital signs monitor is used in such an environment.
Electromagnetic compatibility (EMC): Electromagnetic compatibility (EMC): CARESCAPE V100 monitor Guidance and manufacturer’s declaration – electromagnetic immunity The CARESCAPE V100 vital signs monitor is intended for use in the electromagnetic environment specified below. It is the responsibility of the customer or user to assure that the CARESCAPE V100 vital signs monitor is used in such an environment.
Electromagnetic compatibility (EMC): Electromagnetic compatibility (EMC): CARESCAPE V100 monitor Recommended separation distances The table below provides the recommended separation distances (in meters) between portable and mobile RF communications equipment and the CARESCAPE V100 vital signs monitor. The CARESCAPE V100 vital signs monitor is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled.
Electromagnetic compatibility (EMC): Electromagnetic compatibility (EMC): CARESCAPE V100 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 Healthcare claims EMC compliance.
Electromagnetic compatibility (EMC): Electromagnetic compatibility (EMC): CARESCAPE V100 monitor Part number Description Maximum lengths 2028117-001 SpO2 Sensor, Max-AL Adult Long Finger Adhesive Sensor, 24/box Not specified 414248-001 OXIBAND (OXI-P/I) Pediatric/Infant Sensor Not specified 414248-002 OXIBAND (OXI-A/N) Adult/Pediatric Sensor Not specified 2017002-001 Masimo LNOP, SpO2 cable assembly 3.6 m / 12 ft 2017002-003 Masimo LNOP, SpO2 cable assembly 2.4 m / 7.
Electromagnetic compatibility (EMC): Electromagnetic compatibility (EMC): CARESCAPE V100 monitor Part number Description Maximum lengths TS-E-D TruSignal Ear Sensor 1.0 m / 3.3 ft TS-W-D TruSignal Wrap Sensor 1.0 m / 3.3 ft TS-SE-3 TruSignal Sensitive Skin Sensor 1.0 m / 3.3 ft TS-AF-10 TruSignal AllFit Sensor, 10/box 0.5 m / 1.6 ft TS-AF-25 TruSignal AllFit Sensor, 25/box 0.5 m / 1.6 ft TS-G3 TruSignal Interconnect cable with GE connector 3.0 m / 9.
Asia 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 GE Medical Systems Information Technologies, GmbH Munzingerstrasse 5 79111 Freiburg Germany Tel: + 49 761 45 43 - 0 Fax: + 49 761 45 43 - 233 GE Medical Systems Information Technologies, Inc. Asia; GE (China) Co., Ltd. No1 Huatuo Road, Zhangjiang Hi-tech Park Pudong Shanghai, P.R.
