GE Healthcare CARESCAPE™ V100 Vital Signs Monitor Operator’s Manual CARESCAPE V100 Vital Signs Monitor English 2036991-001 C (paper) © 2007 General Electric Company. All Rights Reserved.
Contents 1 Introduction Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Indications for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Contraindication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Product Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6 Symbols . . . . .
3 Product Overview Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3 Front Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4 Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5 Right-Side Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Battery Low Shutdown and System Failure Sounds . . . . . . . . . . . . . . . . 3-12 Battery Charger Sounds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12 Power Sources . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13 4 Printer Description . . . . . . . . . . . . . . . . . . . . . . . . . . . .
History Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3 Buttons Associated with History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4 Erasing Stored History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4 Windows Associated with History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4 Indicators Associated with History . . . . . . . . . . .
8 Ohmeda TruSignal SpO2 Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3 TruSignal Enhanced SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-3 PIr pulsatile value . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-3 Configuration Settings Associated with SpO2 . . . . . . . . . . . . . . . . . . . . . . 8-5 Buttons Associated with SpO2 . . . . . . . . .
SpO2 Hold-off Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-8 Alarm Timer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-8 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-9 Factory Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-11 Nellcor Patents . . . . . . . . .
Indicators Associated with Temperature . . . . . . . . . . . . . . . . . . . . . . . . . Measurement in Progress Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Predictive Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Monitor Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Measurement NOT in Progress Indicators . . . . . . . . . . . . . . . . . . . . . . . . .
Disposal of Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-5 Storage, Care, and Replacement of Batteries . . . . . . . . . . . . . . . . . . . . . . 13-5 Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-6 Battery Low . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-6 When about 45 minutes of battery charge remains: . . . .
Packing Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-9 Disposal of Product Waste . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-9 Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-9 Patient Applied Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-9 Monitor . . . . . . . . . . . . . . .
x CARESCAPE V100 Vital Signs Monitor 2036991-001C
GE Healthcare CARESCAPE™ V100 Vital Signs Monitor Operator’s Manual CARESCAPE V100 Vital Signs Monitor English 2036991-001 C (paper) © 2007 General Electric Company. All Rights Reserved.
NOTE: The information in this manual also applies to CARESCAPE V100 Vital Signs Monitor software version RAA. There are no user-apparent differences among these software versions. 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. Listed below are GE Medical Systems Information Technologies trademarks.
1 Introduction
Silence Systolic HIGH ADULT LOW Alarms Inflate/Stop MAP/Cuff NEONATE Diastolic Cycle AUTO CYCLE HIGH History HISTORY LOW Menu INFLATE PRESSURE ALARM VOLUME PULSE VOLUME BATTERY OK Pulse Rate HIGH LOW SpO Print BATTERY LOW CHARGING On / Off Temperature HIGH C LOW F CARESCAPE V100 Vital Signs Monitor 1-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Introduction: Description 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 V100 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.
Introduction: Contraindication WARNINGS Do not use the V100 Monitor in the presence of magnetic resonance imaging (MRI) devices. There have been reports of sensors causing patient burns when operating in an MRI environment. Do not use the monitor in the presence of flammable anesthetics. The use of approved accessories will provide protection from burns during HF surgery.
Introduction: Contraindication CAUTIONS Federal law (U.S.A.) restricts this device to sale by or on the order of a physician. Do not use replacement batteries other than the type supplied with the monitor. Use only batteries recommended by GE Medical Systems Information Technologies. Other batteries could result in monitor shut down. Replacement batteries are available from GE Medical Systems Information TechnologiesAccessories and Supplies.
Introduction: Product Compliance Product Compliance The CARESCAPE V100 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 Sterilization/Disinfection, see Appendix C
Introduction: Symbols Symbols The following symbols are associated with the V100 Vital Signs Monitor. NOTE: The model of the monitor determines which symbols appear on it.
Introduction: Symbols WASTE OF ELECTRICAL AND ELECTRONIC EQUIPMENT (WEEE): This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment. Manufacturer: This symbol is accompanied by the name and the address of the manufacturer.
2 Getting Started
For your notes 2-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Getting Started: Unpacking the Monitor and Accessories Unpacking the Monitor and Accessories Before attempting to use the V100 Monitor, take a few minutes to become acquainted with the monitor and its accessories. Unpack the items carefully. This is also a good time to check for any damage or accessory shortage. If there is a problem or shortage, contact GE Medical Systems Information Technologies.
Getting Started: Setting up SpO2 Connections NOTE: Care should be taken in reconnecting the cuff to a hose, ensuring that threads of the cuff and hose are in alignment and no crossthreading occurs. 5. Refer to the “NIBP” Section of this manual for complete instructions on taking an accurate NIBP determination. NOTES Use only GE CRITIKON BP cuffs. The size, shape, and bladder characteristics can affect the performance of the instrument. Inaccurate readings may occur unless GE CRITIKON BP cuffs are used.
Getting Started: Setting up the Printer (Installing the Paper) Setting up the Printer (Installing the Paper) 1. With the monitor powered on, turn it so that the side with the printer is facing you. 2. While grasping the side of the monitor, lift the printer door open by placing your thumb in the indented area and pulling. The printer door will pop open. 3.
Getting Started: Procedure for Testing Alarms WARNINGS If any of the seven-segment indicator lights fail to illuminate during the display test, the accuracy of vital sign values could be misread. Contact GE Medical Systems Information Technologies Technical Support. If the monitor fails to sound the start-up tones, do not use the monitor. This indicates problems with the audible alarm circuit. Contact GE Medical Systems Information Technologies Technical Support.
Getting Started: Configuration Mode Settings Configuration Mode Settings Monitor settings such as HIGH/LOW alarm settings changed in the clinical mode will not be retained after the monitor is powered off. To retain alarm and parameter settings, the changes must be done in the configuration mode. Date/ Time settings are also entered in the configuration mode. Entering Configuration Mode 1.
Getting Started: Setting the Date and Time Setting Setting LED Window Temperature °C or °F Year Systolic Month MAP/Cuff Day Diastolic Hour min Minute min Mode (when main screen is active) LED Display Systolic Setting the Date and Time To set the date and time on the V100 Monitor, you must access the configuration mode. Press Menu to skip the default settings that do not require changes. Refer to the above table.
Getting Started: SpO2 Configuration Settings SpO2 Configuration Settings Procedure for Units With Ohmeda TruSignal Technology (Refer to the “Ohmeda TruSignal SpO2” Section for options) 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. Press the Menu button until LF appears in the Pulse Rate window. 3. Use the +/- buttons to select the option. 4. To exit the configuration mode, turn the unit off.
Getting Started: SpO2 Configuration Settings 2-10 CARESCAPE V100 Vital Signs Monitor 2036991-001C
3 Product Overview
For your notes 3-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Product Overview: Buttons Buttons 1. Silence button: mutes audible alarms. Any other active alarm that can be acknowledged is also removed whenever this key is pressed. When pressed, the silence icon (bell) lights red to indicate that audible alarms have been silenced for 2 minutes. Alarm silence can be cancelled by pressing the Silence button again. 2. Alarms button: used to view or adjust parameter alarm limit settings. 3.
Product Overview: Front Panel 12. Print button: prints currently displayed values or all stored entries when in history mode. 13. On/Off button: controls on/off state of monitor; push for power on and push again for power off. 14. Temperature probe connector: attach temperature probe cable here.
Product Overview: Rear Panel 27. AUTO CYCLE indicator: lights green to indicate auto mode is the chosen NIBP mode; flashes to indicate you are making a change to the auto mode. 28. Min window: displays the NIBP mode if manual or Stat as well as the cycle time when taking auto NIBP determinations. 29. HISTORY indicator: flashes to indicate you are in history mode. 30. BATTERY OK indicator: lights green to indicate the monitor is operating on battery power and that the battery is sufficiently charged. 31.
Product Overview: Right-Side Panel Right-Side Panel 36 36. External DC power socket: used with approved GE Medical Systems Information Technologies AC-DC power converter ONLY. Windows Each derived vital sign has an associated window for displaying the value. For each window, the vital sign’s name and unit of measure are labeled above and to the right of it, respectively. An additional window--the min window--is available for displaying the NIBP mode or chosen AUTO CYCLE selection.
Product Overview: Operating (System) Modes Clinical Mode Clinical mode is the mode used to monitor patients. How to enter and exit clinical mode To enter clinical mode: With the monitor off, press the On/Off button. To exit clinical mode: With the monitor on, press the On/Off button for less than 5 seconds. While in clinical mode: All parameters are available for monitoring. Alarm limits and all user settings are adjustable.
Product Overview: User Modes Advanced Configuration Mode Advanced configuration is used for configuring the monitor’s serial port communication settings as well as viewing and printing the failure alarm history. Advanced configuration mode displays the software revision in the Systolic and Diastolic windows.
Product Overview: User Modes Menu Mode The menu mode allows you to access and change the three settings associated with the following indicators: INFLATE PRESSURE (ADULT and NEONATE), ALARM VOLUME, and PULSE VOLUME. To enter this mode, press the Menu button. Each press of the Menu button steps you through each of the these settings. After 7 seconds of not pressing the Menu button, the menu mode is automatically exited. Otherwise, you can exit the menu mode by cycling through all menu options.
Product Overview: User Modes Cycle Mode The cycle mode allows you to start auto cycle and Stat modes. 1. Press the Cycle button. The AUTO CYCLE indicator flashes. 2. To change the time increment while the AUTO CYCLE indicator flashes, simply use the +/- button to increment or decrement, respectively. When you reach the beginning or ending of the list, the negative key-click sounds. OR 3.
Product Overview: Sounds History Mode The history mode allows you to access the stored patient data. When the history mode is active, pressing the +/- buttons displays the next or previous entry in the history list. When you reach the beginning or end of the list, a negative key-click sounds. Pressing the History button also allows you to view the previous entry. NOTE: Refer to the “History” Section for more information.
Product Overview: Power Sources Medium priority The medium-priority alarm sounds three high-pitched tones. Low priority The low-priority alarm sounds one single tone. Battery Low Shutdown and System Failure Sounds When the monitor enters either of these modes, it generates a sound that remains on until the monitor either automatically shuts down or is turned off. This sound consists of a high-pitched tone that repeats at a very high rate.
Product Overview: Specifications Specifications Specifications Mechanical Dimensions Height 7.7 in (19.5 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) 5.4 lb (2.
Product Overview: Specifications 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 (2001) Medical Electrical Equipment, Electromagnetic Compatibility Requirements and Tests and CISPR 11 (Group 1, Class B) for radiated and conducted emissions 3-14 CARESCAPE V100 Vital Signs Monitor 2036991-001C
4 Printer
For your notes 4-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Printer: Description Description The printer is an optional feature to the V100 Monitor. If your monitor contains a printer, each time a printout is started the following information is printed. Monitor name and model Current software revision Area for patient name and handwritten comments Column and parameter labels Date and time Unit of measure Vital signs data, if available Installing the Paper Refer to the “Getting Started” Section for instructions.
Printer: Printouts The availability of the printer is determined at the time the printout is started. When the printer is unavailable: The Print button makes a negative key sound when you press it. Printouts of any type are not available and a high-priority E13 BATTERY LOW alarm sounds when the BATTERY LOW indicator flashes. The printer is unavailable if it is out of paper, too hot, or if the monitor is in any of the following modes: cycle, alarm limit adjustment, menu, config, or service.
Printer: Paper Storage Clinical History All entries currently stored in the clinical history list when the Print button is pressed are printed in the order of the most recent (newest) to the oldest. For a value that was violating its high limit when it was stored, an up arrow is printed after the value. For a value that was violating its low limit when it was stored, a down arrow is printed after that value. If the date changes between entries, a single line containing the date is printed.
Printer: Alarms 4-6 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Printer: Specifications Specifications Specifications Printer type Thermal dot array Resolution 384 dots/inch horizontal Paper type The paper roll used by the printer must be compatible with GE PN 770137.
Printer: Specifications 4-8 CARESCAPE V100 Vital Signs Monitor 2036991-001C
5 Alarms
For your notes 5-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Alarms: Description Description The V100 Monitor provides visible and audible indications of patient- and system-related alarm conditions. An alarm can generate an audible indication, visual indication, alarm message code, and electronic record in the history. There are three categories of alarms: patient-related (limit and parameter status alarms), system-related (printer, battery, and memory alarms), and system failures.
Alarms: Silencing and Acknowledging an Alarm Silencing and Acknowledging an Alarm Silence Button To silence a patient-related alarm (limit and parameter status alarms) at anytime, press the Silence button. The silence icon (a bell) lights red to indicate that audible alarms have been silenced for 2 minutes. Some patient- and system-related alarms are acknowledgeable. (Refer to the Alarms Table at the back of this section.
Alarms: Alarms and Priorities Limit Alarms The monitor checks each derived vital sign (except MAP and temperature) against user-set limits. A high-limit alarm is generated when that value is greater than its high limit. A low-limit alarm is generated when that value is less than its low limit. All limit alarms are considered high priority.
Alarms: Alarms and Priorities Memory Alarm The E00 MEMORY LOST alarm is generated on power-up when battery backed RAM has been corrupted. When it occurs, all settings are reset to their factory defaults and all entries in clinical history are erased. This alarm is generated as a high-priority alarm.
Alarms: Alarms Alarms Alarm message code (if any) Alarm detected Cause Alarm category Acknowledgeable by pressing Silence?* NIBP NIBP SYSTOLIC HIGH Value is greater than the HIGH alarm limit limit yes NIBP SYSTOLIC LOW Value is less than the LOW alarm limit limit yes NIBP DIASTOLIC HIGH Value is greater than the HIGH alarm limit limit yes NIBP DIASTOLIC LOW Value is less than the LOW alarm limit limit yes E89 NIBP NO DETERMINATION NIBP failed.
Alarms: Factory Defaults Alarm message code (if any) Alarm detected Cause Alarm category Acknowledgeable by pressing Silence?* Pulse rate PULSE RATE HIGH Value is greater than the HIGH alarm limit limit no-SpO2, yes-NIBP PULSE RATE LOW Value is less than the LOW alarm limit limit no-SpO2, yes-NIBP E10 PRINTER NO PAPER Printer no paper status yes E11 PRINTER TOO HOT Printer too hot status yes BATTERY LOW Battery too low status yes BATTERY LOW Battery is running low and should be
6 History
For your notes 6-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
History: Description Description NOTE: Age in this section refers to when and how long ago the vital signs were taken. The history mode allows you to access stored patient data in clinical mode and a failure alarm history in advanced configuration mode.
History: Buttons Associated with History Buttons Associated with History To activate the history mode, press the History button. The HISTORY indicator flashes green while this mode is active. With each press of the History button, the patient data stored with the next oldest entry is displayed. Entries are displayed from the most recent to the oldest. For example, the most recent entry could have an age of -0 minutes and the oldest entry could have an age of 23:59.
7 NIBP
For your notes 7-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
NIBP: Description Description NOTE: Age in this section refers to how long ago the vital signs were taken. The NIBP parameter in the V100 Monitor is available with two types of NIBP technologies: one calibrated to intra-arterial pressure (DINAMAP SuperSTAT or Classic) and one calibrated to the auscultatory method (specific technologies are available in select markets).
NIBP: Description What is the Difference Between Intra-Arterial and Auscultatory Methods? Oscillometric Method The oscillometric method of determining NIBP is accomplished by a sensitive transducer which measures cuff pressure and pressure oscillations within the cuff. These signals are analyzed by the algorithm that uses one of the references (intra-arterial or auscultatory) to display the NIBP values.
NIBP: Description WARNINGS The values displayed on the monitor could be up to 30 minutes old in manual mode and 120 minutes old in auto mode. If the patient’s condition has changed between one determination and the next, the monitor will not detect the change until the next determination is taken. Use care when placing cuff on extremity used to monitor other patient parameters. The V100 Monitor is designed for use only with GE CRITIKON BP dual-tube cuffs.
NIBP: Buttons Associated with NIBP NOTES A patient’s vital signs may vary dramatically during the use of cardiovascular agents such as those that raise or lower blood pressure or those that increase or decrease heart rate. Several conditions may cause the NIBP parameter to calculate and display only the mean arterial pressure (MAP) without systolic and diastolic readings. These conditions include very low systolic and amplitude fluctuations, so an accurate calculation for these values can’t be made (e.g.
NIBP: Windows Associated with NIBP Pressing this button key while the BATTERY LOW alarm is active as a highpriority alarm results in the generation of the E13 BATTERY LOW alarm and the sounding of the negative key tone. Windows Associated with NIBP The windows associated with NIBP are Systolic, Diastolic, MAP/Cuff, Pulse Rate, and min. The Systolic, Diastolic, MAP/Cuff, and Pulse Rate (if SpO2 is not active) windows are automatically cleared when a new NIBP determination is started.
NIBP: NIBP Modes of Operation NIBP Modes of Operation The V100 Monitor has three NIBP modes: 1. Manual 2. Auto cycle 3. Stat The mode is selected by the user. NIBP determinations are automated and, upon completion, the values for systolic pressure, diastolic pressure, mean arterial pressure, and pulse rate (if SpO2 is not active) are shown in their respective windows. Manual NIBP Determinations Manual mode is always the NIBP mode of operation upon power-up.
NIBP: User Settings cycle mode is deactivated. Press the Inflate/Stop button to stop the determination in progress without canceling the auto cycle mode. Choose the two dashes (- -) to cancel auto cycle mode. If an auto cycle determination results in a limit alarm, a repeat determination is taken to verify the alarm. Only the first determination in a series of limit alarms will be followed by a repeat determination.
NIBP: Menu Settings Limit Settings There are two limit settings associated with this parameter: HIGH and LOW. Both limit settings are available for Systolic and Diastolic windows, as well as Pulse Rate (refer to the “Pulse Rate” Section). The settings appear in increments of 5 mmHg. Systolic and Diastolic limits are adjustable for adult/ped and neonate patient types. The ADULT indicator is solid green while Systolic and Diastolic limits for adult/pediatric are being adjusted.
NIBP: Sounds Associated with NIBP Changing this setting for either patient type cancels a determination that is in progress and clears previously derived Systolic, Diastolic and MAP values in their associated windows. The appropriate target inflation pressure for the next determination is used when any of the following are true: A current valid MAP value is not displayed. In manual mode and the last determination is greater than 2 minutes old.
NIBP: Procedures Add 1.80 mmHg to values for every inch (2.54 cm) above heart level. Subtract 1.80 mmHg from values for every inch (2.54 cm) below heart level. 4. Select appropriate cuff size. Measure patient’s limb and select appropriately sized cuff according to size marked on cuff or cuff packaging. When cuff sizes overlap for a specified circumference, choose the larger size cuff. CAUTIONS Accuracy depends on use of proper size cuff. NOTE: Use only GE CRITIKON BP cuffs.
NIBP: Alarms What to do When Taking NIBPs on Different Patients To ensure the previous patient’s NIBP will not be used for adaptive target inflation pressure when taking an NIBP on a new patient, you can 1.) clear the history by holding the history key for more than 2 seconds, or 2.) if in manual mode, wait for more than 2 minutes since the last determination was taken on the previous patient.
NIBP: Alarms 7-14 CARESCAPE V100 Vital Signs Monitor 2036991-001C
NIBP: Specifications Specifications Specifications Cuff pressure range (Normal operating range) 0 to 290 mmHg (adult/ped 0 to 145 mmHg (neonate) Blood pressure accuracy (Classic and Auscultatory) Meets ANSI/AAMI standard SP-10:1992 (mean error ≤ 5 mmHg, standard deviation ≤ 8 mmHg) Blood pressure accuracy (SuperSTAT) Meets ANSI/AAMI standard SP-10:2002 (mean error ≤ 5 mmHg, standard deviation ≤ 8 mmHg) Maximum determination 120 s (adult/ped) 85 s (neonate) Overpressure cutoff 300 to 330 mmHg (adul
NIBP: Specifications Factory Defaults Adult/ped Neonate Non-patient Specific Systolic (mmHg) HIGH 200 100 LOW 80 40 HIGH 120 60 LOW 30 20 Inflation pressure (for Auscultatory) 160 100 Inflation pressure (for SuperSTAT) 135 100 Inflation pressure (for Classic) 160 110 Diastolic (mmHg) Cycle button default 15 min GE Medical Systems Information Technologies Patents 5,170,795; 5,704,362; 5,518,870; 5,579,776; 6,358,213; 6,746,403; 6,893,403; 6,902,531; 7,070,566; 7,074,192; 7,186,218
8 Ohmeda TruSignal SpO2
For your notes 8-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Ohmeda TruSignal SpO2: Description Description The SpO2 parameter in the V100 Monitor is available in three different leading technologies: Ohmeda TruSignal, Nellcor and Masimo SET. Please refer to the front of your monitor to see which SpO2 technology your monitor contains. If your monitor contains this parameter, the SpO2 technology logo will be on the front fascia of the monitor. This section refers to Ohmeda TruSignal SpO2 technology.
Ohmeda TruSignal SpO2: Description The perfusion index is only available on a current printout and when the sensor is in place; it does not appear on the monitor screen. On the PIr info line, a row is printed that contains the time the Print button was pressed followed by the current perfusion index measurement when it is valid. WARNINGS Do not place SpO2 sensor on patient during magnetic resonance imaging (MRI).
Ohmeda TruSignal SpO2: Configuration Settings Associated with SpO2 CAUTIONS Do not perform any testing or maintenance on a sensor while it is being used to monitor a patient. Bright light sources (e.g., infrared heat lamps, bilirubin lights, direct sunlight, operating room lights) may interfere with the performance of the SpO2 function. To prevent such interference, cover the sensor with opaque material.
Ohmeda TruSignal SpO2: Windows Associated with SpO2 Windows Associated with SpO2 There is one window associated with this parameter: SpO2. While in offline mode, nothing is displayed in the SpO2 window. When in ready mode and the parameter senses that a sensor is connected, a single dash (-) appears in this window. When it is in operate mode and the parameter is reporting a valid data, the derived SpO2 value appears in this window and updates continuously. The values are displayed in %.
Ohmeda TruSignal SpO2: Procedures Procedures 1. Select a sensor that is appropriate for the patient and the clinical situation. NOTE: Use only TruSignal OxiTip+ sensors and interconnect cables. Use of another pulse oximetry cable will have an adverse effect on performance. Do not attach any cable that is intended for computer use to the sensor port. Do not connect any device other than TruSignal-approved sensor to the sensor connector.
Ohmeda TruSignal SpO2: Alarms CAUTIONS Patient safety: Do not place any clip-on sensor in a patient’s mouth or on a patient’s nose or toe. Do not place a clip-on finger sensor on a patient’s thumb or across a child’s foot or hand. The sensor disconnect error message and associated alarm indicate that the sensor is either disconnected or the wiring is faulty. The user should check the sensor connection and, if necessary, replace the sensor, interconnect cable, or both.
Ohmeda TruSignal SpO2: Specifications Specifications Specifications Measurement range SpO2 1 to 100% Pulse rate 30 to 250 bpm Perfusion range 0.
Ohmeda TruSignal SpO2: Specifications Specifications: Sensor Accuracy SpO2 range 70% to 100% Sensor model OxyTip+ OXY-F-UN ±2 digits without motion OXY-W-UN ±2 digits without motion OXY-E-UN ±2 digits without motion OXY-SE ±2 digits without motion OXY-AP ±2 digits without motion OXY-AF ±2 digits without motion OXY-F2-GE ±2 digits without motion OXY-F4-GE ±2 digits without motion OXY-E2-GE ±2 digits without motion OXY-E4-GE ±2 digits without motion Sensor light source Wavelength* Infra
Ohmeda TruSignal SpO2: Troubleshooting Troubleshooting This section discusses potential difficulties and suggestions for resolving them. If the difficulty persists, contact a qualified service person or your local representative. The service manual, which is for use by qualified service personnel, provides additional troubleshooting information. PROBLEM: The pulse amplitude bar indicates a pulse, but no oxygen saturation or pulse rate values appear on the screen.
Ohmeda TruSignal SpO2: Troubleshooting PROBLEM: The oxygen saturation measurement does not correlate with the value calculated from a blood gas determination. CAUSE: The SpO2 calculation may not have correctly adjusted for the effects of pH; temperature; CO2; fetal hemoglobin; or 2,3-DPG.
Ohmeda TruSignal SpO2: Troubleshooting PROBLEM: An E20 SENSOR DISCONNECTED error code has been detected, but the sensor is still connected. CAUSE: The sensor is not completely connected. The interconnect cable or sensor wiring is faulty. Ensure the appropriate sensor and cable are being used. SOLUTION: Check the patient. Check the sensor connection to the interconnect cable and the interconnect cable connection to the monitor. Then, if needed, replace the sensor or the interconnect cable.
Ohmeda TruSignal SpO2: Troubleshooting 8-14 CARESCAPE V100 Vital Signs Monitor 2036991-001C
9 Nellcor OXIMAX SpO2
For your notes 9-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Nellcor OXIMAX SpO2: Description Description The SpO2 parameter in the V100 Monitor is available in three different leading technologies: Ohmeda TruSignal, Nellcor and Masimo SET. Please refer to the front of your monitor to see which SpO2 technology your monitor contains. If your monitor contains this parameter, the SpO2 technology logo will be on the front fascia of the monitor. This section refers to Nellcor SpO2 technology.
Nellcor OXIMAX SpO2: Configuration Settings Associated with SpO2 WARNINGS Pulse oximetry readings and pulse signals can be affected by certain environmental conditions, sensor application errors, and certain patient conditions. See the appropriate sections of this manual for specific safety information. The use of accessories, transducers, and cables other than those specified may result in increased emission and/or decreased immunity and inaccurate readings of the monitor.
Nellcor OXIMAX SpO2: Buttons Associated with SpO2 SatSeconds™ With traditional alarm management, upper and lower alarm limits are set for monitoring SpO2. During monitoring, as soon as an alarm limit is violated by as little as one percentage point, an audible alarm immediately sounds. When the % SpO2 fluctuates near an alarm limit, the alarm sounds each time the limit is violated. To prevent these nuisance alarms, the V100 Monitor uses the SatSeconds technique.
Nellcor OXIMAX SpO2: User Settings User Settings Limit settings There are two limit settings associated with this parameter: HIGH and LOW. The range for HIGH is 71 to 100%. The range for LOW is 70 to 99%. The settings appear in increments of 1%. Menu Settings The PULSE VOLUME menu setting is associated with the SpO2 parameter. This option lets you adjust the volume of the tone that sounds after each detected pulse. It can be adjusted from 0 - 10 (10 being the loudest).
Nellcor OXIMAX SpO2: Procedures 2. Following the directions for use supplied with the sensor, apply the sensor to the patient. WARNINGS Patient safety: If the sensor is not applied properly, the patient’s skin could be injured or the ability of the V100 Monitor to measure oxygen saturation could be compromised. For example, a clip-on sensor should never be taped shut.
Nellcor OXIMAX SpO2: Alarms 3. Plug the SpO2 sensor into the SpO2 sensor extension cable. Then plug the SpO2 sensor extension cable into the SpO2 sensor connector. 4. Proceed with monitoring. SpO2 measurements run continuously and can run simultaneously with other measurements. Alarms SpO2 Hold-off Period The hold-off period is defined as the 10 seconds that follows when the SpO2 parameter switches from ready mode to operate mode. This hold-off period helps prevent any nuisance alarms.
Nellcor OXIMAX SpO2: Specifications Specifications Specifications Measurement range SpO2 1 to 100% Pulse rate 20 to 250 bpm Perfusion range 0.03 to 20% Accuracy Saturation Adult* 70 to 100% ±2 digits Neonate* 70 to 100% ±3 digits Low perfusion** 70 to 100% ±2 digits Pulse Rate Adult and neonate 40 to 250 bpm ±3 digits Low perfusion** 40 to 250 bpm ±3 digits *Adult specifications are shown for OxiMax MAX-A and MAX-N sensors with the N-600. Saturation accuracy will vary by sensor type.
Nellcor OXIMAX SpO2: Specifications Specifications: Nellcor OXIMAX sensor accuracy SC-A (adult) ± 2 digits SC-PR (neonate) ± 3 digits SC-NEO ± 3 digits MAX-R** ± 3.5 digits OxiCliq OxiCliq A ± 2.5 digits OxiCliq P ± 2.5 digits OxiCliq N (adult) ± 2.5 digits OxiCliq N* (neonate) ± 3.5 digits OxiCliq I ± 2.5 digits Reusable sensor models D-YS (infant to adult) ± 3 digits D-YS (neonate) ± 4 digits D-YS & D-YSE ± 3.5 digits D-YS & D-YSPD ± 3.
Nellcor OXIMAX SpO2: Specifications Factory Default Settings SpO2 (%) HIGH alarm limit 100 SpO2 (%) LOW alarm limit 90 Response mode 1 (for Mode 1: Normal response) SatSeconds™ 0 Nellcor Patents Re.35,122; 4,802,486; 4,869,254; 4,928,692; 4,934,372; 4,960,126; 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 and international equivalents.
Nellcor OXIMAX SpO2: Specifications 9-12 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Nellcor OXIMAX SpO2: Troubleshooting Troubleshooting This section discusses potential difficulties and suggestions for resolving them. If the difficulty persists, contact a qualified service person or your local representative. The service manual, which is for use by qualified service personnel provides additional troubleshooting information. PROBLEM: The pulse amplitude bar indicates a pulse, but no oxygen saturation or pulse rate values appear on the screen.
Nellcor OXIMAX SpO2: Troubleshooting PROBLEM: The oxygen saturation measurement does not correlate with the value calculated from a blood gas determination. CAUSE: The SpO2 calculation may not have correctly adjusted for the effects of pH; temperature; CO2; fetal hemoglobin; or 2,3-DPG.
Nellcor OXIMAX SpO2: Troubleshooting PROBLEM: An E20 SENSOR DISCONNECTED error code has been detected, but the sensor is still connected. CAUSE: The sensor is not completely connected. The sensor extension cable or sensor wiring is faulty. SOLUTION: Check the patient. Check the sensor connection to the sensor extension cable and the sensor extension cable connection to the monitor. Then, if needed, replace the sensor or the sensor extension cable.
Nellcor OXIMAX SpO2: Troubleshooting 9-16 CARESCAPE V100 Vital Signs Monitor 2036991-001C
10 Masimo SET SpO2
For your notes 10-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Masimo SET SpO2: Description Description ® The SpO2 parameter in the V100 Monitor is available in three different leading technologies: Ohmeda TruSignal, Nellcor and Masimo SET. Please refer to the front of your monitor to see which SpO2 technology your monitor contains. If your monitor contains this parameter, the SpO2 technology logo will be on the front fascia of the monitor. This section refers to Masimo SET SpO2 technology.
Masimo SET SpO2: Indications and Contraindications WARNINGS Do not use the SpO2 parameter during magnetic resonance imaging (MRI). Adverse reactions include potential burns to patients as a result of contact with attachments heated by the MRI radio frequency pulse, potential degradation of the magnetic resonance image, and potential reduced accuracy of SpO2 measurements. Always remove oximetry devices and attachments from the MRI environment before scanning a patient.
Masimo SET SpO2: Indications and Contraindications CAUTIONS Loss of pulse signal can occur in any of the following situation: the sensor is too tight there is excessive illumination from light sources such as surgical lamp, a bilirubin lamp, or sunlight a blood pressure cuff is inflated on the same extremity as the one with a SpO2 sensor attached the patient has hypotension, severe vasoconstriction, severe anemia, or hypothermia there is arterial occlusion proximal to the sensor the patient is in cardiac a
Masimo SET SpO2: Configuration Settings Associated with SpO2 NOTES A patient’s vital signs may vary dramatically during the use of cardiovascular agents such as those that raise or lower blood pressure or those that increase or decrease pulse rate. The V100 Vital Signs Monitor that is labeled with Masimo SET Technology is compatible only with Masimo SET sensors. Software development, software validation, and Risk and Hazard Analysis has been performed to a registered quality system.
Masimo SET SpO2: Indicators Associated with SpO2 Indicators Associated with SpO2 There is one indicator associated with this parameter: the pulse amplitude indicator bar. The red LED bar flashes to indicate that pulse rate measurements are being derived from SpO2 signals and the height of the bar is proportional to the arterial blood flow. User Settings Limit settings There are two limit settings associated with this parameter: HIGH and LOW. The range for HIGH is 71 to 100%.
Masimo SET SpO2: Procedures 2. Following the directions for use supplied with the sensor, apply the sensor to the patient. WARNINGS Patient safety: If you fail to apply the sensor properly, the patient’s skin could be injured or the ability of the V100 Monitor to measure oxygen saturation could be compromised. For example, a clip-on sensor should never be taped shut.
Masimo SET SpO2: Alarms Alarms SpO2 Hold-off Period The hold-off period is defined as the 10 seconds that follows when the SpO2 parameter switches from ready mode to operate mode. This hold-off period helps prevent any nuisance alarms. Parameter status alarms are not displayed and the derived SpO2 value is not checked against user-set limits while the SpO2 hold-off period is active. Alarm Timer When an SpO2 sensor is on for less than 2 minutes this is considered "spot mode.
Masimo SET SpO2: Alarms 10-10 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Masimo SET SpO2: Specifications Specifications Specifications Measurement range SpO2 1 to 100% Pulse rate 25 to 240 bpm Perfusion range 0.
Masimo SET SpO2: 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 Foot Finger ± 3 digits without m
Masimo SET SpO2: Specifications Specifications: Masimo sensor accuracy LNCS Neo PT-L ± 3 digits without motion Resolution Saturation (% SpO2) 1% Pulse rate (bpm) 1 Low perfusion performance 0.02% Pulse amplitude and % transmission >5% Saturation (% SpO2) ±2 digits Pulse rate ±3 digits Interfering substances Carboxyhemoglobin may erroneously increase readings. The level of increase is approximately equal to the amount of carboxyhemoglobin present.
Masimo SET SpO2: Specifications Factory Default Settings 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) Masimo Patents 5,823,950; 5,758,644; 6,011,986; 6,501,975; 6,157,850; 6,263,222 and other applicable patents listed at: www.masimo.com/patents.htm.
Masimo SET SpO2: Troubleshooting Troubleshooting This section discusses potential difficulties and suggestions for resolving them. If the difficulty persists, contact a qualified service person or your local representative. The service manual, which is for use by qualified service personnel, provides additional troubleshooting information. PROBLEM: The pulse amplitude bar indicates a pulse, but no oxygen saturation or pulse rate values appear on the screen.
Masimo SET SpO2: Troubleshooting PROBLEM: The oxygen saturation measurement does not correlate with the value calculated from a blood gas determination. CAUSE: The SpO2 calculation may not have correctly adjusted for the effects of pH; temperature; CO2; fetal hemoglobin; or 2,3-DPG.
11 Alaris Turbo Temp
For your notes 11-2 CARESCAPE V100 Vital Signs Monitor 2036691-001C
Alaris Turbo Temp: Description Description The V100 Monitor uses Alaris Turbo Temp technology (if your monitor has this parameter) and can be used with both oral and rectal temperature probes. The Alaris Turbo Temp parameter consists of an electronic thermometer that uses a temperature-sensing device known as a thermistor. The thermistor is part of the electrical circuit and is located at the tip of the probe.
Alaris Turbo Temp: Description NOTE: These temperature readings are not stored in history, printed, or reported via host comms. WARNING The performance of the monitor may be degraded if it is operated outside of the environmental conditions specified in Product Overview. CAUTIONS Be careful not to overextend the coiled cord of the temperature probe. Overextension can damage the probe coil connector interfaces.
Alaris Turbo Temp: Configuration Settings Associated with Temperature Configuration Settings Associated with Temperature There is one configuration setting associated with this parameter: Unit of Measure (Unt). This setting allows you to choose °Fahrenheit (F) or °Celsius (C). Buttons Associated with Temperature There are no buttons associated with this parameter. Windows Associated with Temperature The Temperature window displays the value in °C or °F.
Alaris Turbo Temp: User Settings Monitor Mode The temperature value flashes indicating monitor mode. Four dashes flash in the Temperature window indicating that the measurement is < 80.0°F. Measurement NOT in Progress Indicators Two dashes appear in the center of the Temperature window indicating no values are present, and the probe is connected. Blank: The Temperature window appears blank indicating that no probe is connected. User Settings There are no user settings associated with this parameter.
Alaris Turbo Temp: Procedures for Oral Predictive Mode Determinations Procedures for Oral Predictive Mode Determinations For oral temperature measurement, use the blue oral probe. 1. Connect the temperature probe cable to the temperature probe connector. 2. Remove the temperature probe from the probe holster. An audible singletone sounds. Place a protective temperature probe cover on the probe. 3.
Alaris Turbo Temp: Procedures for Rectal Predictive Mode Determinations Procedures for Rectal Predictive Mode Determinations For rectal temperature measurement use the red rectal probe. 1. Connect the temperature probe cable to the temperature probe connector. 2. Remove the temperature probe from the probe holster. An audible singletone sounds. Place a protective temperature probe cover on the probe.
Alaris Turbo Temp: Procedures for Monitor Mode Determinations (Axillary Determinations) holster. When monitor mode is activated, an audible double-tone sounds and flashing numbers appear in the Temperature window. Place a protective temperature probe cover on the probe and insert the probe in the patient's axilla, making sure the tip of the probe is in contact with the skin and positioned as close as possible to the axillary artery with the patient's arm held close to his/her side. 3.
Alaris Turbo Temp: Procedures for Monitor Mode Determinations (Axillary Determinations) 11-10 CARESCAPE V100 Vital Signs Monitor 2036691-001C
Alaris Turbo Temp: Specifications Specifications Specifications Scale °Fahrenheit (F)° °Celsius (C) Range Predictive mode Max: 41.1°C; 106.0°F Min: 35.6°C; 96.0°F Monitor mode Max: 41.1°C; 106.0°F Min: 26.7°C; 80.0°F Monitor mode accuracy ±0.1°C ±0.2°F (when tested in a calibrated liquid bath; meets ASTM E1112, Table 1, in range specified) Determination time approx. 10 seconds, typical NOTE: Use only IVAC probes and P850A probe covers.
Alaris Turbo Temp: Specifications 11-12 CARESCAPE V100 Vital Signs Monitor 2036691-001C
12 Pulse Rate
For your notes 12-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Pulse Rate: Description Description The Pulse Rate parameter is included in all Models. Pulse rate values can be derived from one of two sources. In descending order of priority, they are pulse oximetry (SpO2) and noninvasive blood pressure (NIBP). The derived values for pulse rate appear in the Pulse Rate window. While SpO2 is in operate mode, SpO2 is the primary source of the pulse rate.
Pulse Rate: Indicators Associated with Pulse Rate Indicators Associated with Pulse Rate The indicators associated with pulse rate are HIGH and LOW. Refer to “Limit Settings” in this section. User Settings Limit settings There are two limit settings associated with this parameter: HIGH and LOW. The range for all sources (NIBP and SpO2 is the same: HIGH 35 to 235 bpm and LOW is 30 to 230 bpm. The settings appear in increments of 5 bpm.
13 Battery
For your notes 13-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Battery: Description Description The CARESCAPE V100 Vital Signs Monitor uses an internal battery. The battery is a sealed lead acid battery that can be charged at any time without fear of reducing its charge capacity. The monitor is always powered by the battery; and the battery is constantly being charged whenever the external DC charger is connected. The V100 Monitor is designed to operate from an internal lead-acid battery (see “Specifications” in “Product Overview” Section).
Battery: Buttons Associated With the Battery Buttons Associated With the Battery There are no buttons associated with the battery. Windows Associated With the Battery There are no windows associated with the battery. Indicators Associated With the Battery When the monitor is on, the DC charger is not attached, and the battery is sufficiently charged, the BATTERY OK indicator is backlit green. Unless specified otherwise, at all other times this indicator is turned off.
Battery: Disposal of Batteries Battery charging will take place as long as the monitor remains connected to an external DC power source. Sys to lic HIGH Cuff olic AUTO HIGH LOW Charge battery pack for 12 hours before first use or after prolonged periods of storage. MAP/ LOW Diast Pulse CYCL E HISTO RY Rate HIGH LOW SpO HIGH LOW Tem pera ture C F If the monitor is idle for extended periods, it should be fully charged at least once a month to ensure optimum performance.
Battery: Alarms Alarms Battery Low When about 45 minutes of battery charge remains: The low-priority BATTERY LOW alarm is issued. The BATTERY LOW indicator illuminates. This alarm can be silenced by pressing the Silence button. The BATTERY LOW alarm will re-alarm every 10 minutes after it’s been silenced. If the alarm is not silenced, the alarm is re-issued every 8 seconds. The monitor continues to operate normally.
Battery: Alarms After plugging the monitor into DC power: The BATTERY LOW indicator (when the monitor is on) and CHARGING indicator illuminate. The BATTERY LOW indicator turns off when the battery level reaches a sufficient charge level to operate without the BATTERY LOW alarm active. E13 Battery Low At any time while the high-priority BATTERY LOW alarm is active, certain actions can trigger the E13 BATTERY LOW alarm: any attempt to start an NIBP determination or a printout.
Battery: Alarms 13-8 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Battery: Specifications Specifications Specifications Capacity 6V; 3.3 Ahr sealed lead acid battery Battery life 8.1 hours (standard deviation of 0.46) with a usage scenario of: NIBP determinations every 15 minutes with SpO2 and temperature active. 11.5 hours (standard deviation of 0.53) non-SpO2 versions with a usage scenario of: NIBP determinations every 15 minutes with temperature active Charge time 2036991-001C Approx. 5 hours from full discharge when the monitor is off Approx.
Battery: Specifications 13-10 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Battery: Troubleshooting Troubleshooting This section discusses potential difficulties and suggestions for resolving them. If the difficulty persists, contact a qualified service person or your local GE Medical Systems Information Technologies representative. The service manual, which is for use by qualified service personnel, provides additional troubleshooting information. PROBLEM: The battery does not work or does not last very long.
Battery: Troubleshooting PROBLEM: The BATTERY LOW indicator remains lit or flashing. CAUSE: The battery is unable to recharge. SOLUTION: The battery needs to be recalibrated or is defective. To recalibrate, simply recharge the battery by plugging the external DC charger into the monitor. The recharge time may vary depending upon the current battery charge status.
A Connections
For your notes A-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Connections: Connection Details Connection Details Host Port Connector (rear panel) WARNING! Auxiliary equipment connected to the CARESCAPE V100 Monitor will result in the formation of an electromedical system and thus, must comply with the requirements of EN 60601-1-1/ IEC 60601-1. All host port signals are NONISOLATED and should be connected to equipment conforming to IEC-60601-1, configured to comply with IEC 60601-1-1 ONLY.
Connections: Connection Details A-4 CARESCAPE V100 Vital Signs Monitor 2036991-001C
B Accessories
For your notes B-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Accessories: Accessories Accessories Part Part description Part number NIBP NIBP, Adult, 12ft Air hose adult/ped 12 ft, gray 107365 NIBP, Neonate, 12ft Air hose, neonatal 12 ft, light blue 107368 NIBP, Adult, 24ft Air hose adult/ped 24 ft, gray 107366 NIBP, Cuff, Classic Cuff, Neonate Classic-Cuf, assortment pack, neonatal, 2-tube, M slip 2693 NIBP, Cuff, Classic Cuff, Various Classic-Cuf, assortment pack, various, 2-tube, screw 2692 NIBP, Cuff, Soft Cuff, Various Soft-Cuf, assortment pa
Accessories: Accessories Part Part description Part number SpO2 - Accessory Foam wrap replacement, small, weight range < 3 kg OXY-RWS SpO2 - Accessory OxyTip+ replacement tape, AllFit Sensor, Bears - 100/box OXY-RTB SpO2 - Accessory OxyTip+ replacement tape, AllFit Sensor, Blue - 100/box OXY-RT SpO2 - Accessory Infant Foam Sandal, use with OxyTip+ Sensitive Skin sensor - 3/box OXY-SND SpO2 Cable Assy 3M Cable Assy SpO2 Nellcor OxiMax 3 m - Smart 2021406-001 SpO2 Cable Assy 3M Cable Assy
Accessories: Accessories Part Part description Part number SpO2 - Sensor Masimo LNOP Disposable Adhesive Sensor Bridge, LNOP Neo. Neonatal - 20/box 2010460-001 SpO2 - Sensor Masimo LNOP Disposable Adhesive Sensor, LNOP-Neo-L. Neonatal - 20/box 2017089-001 SpO2 - Sensor Masimo LNOP Disposable Adhesive Sensor, LNOP NeoPT-L.
Accessories: Accessories Part Part description Part number SpO2 - Accessory Masimo Replacement Posey Wrap, LNOP-NeoPt-L, Neonatal - 12/box 2010466-001 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 Masim
Accessories: Accessories Part Part description Part number Manuals Operation Manual - Paper CARESCAPE V100 Operator’s Manual, Hard Copy 2036991-001 Service Manual - Paper CARESCAPE V100 Service Manual, Hard Copy 2037106-001 Service Manual - CD CARESCAPE V100 Service Manual, CD 2037107-001 2036991-001C CARESCAPE V100 Vital Signs Monitor B-7
Accessories: Accessories B-8 CARESCAPE V100 Vital Signs Monitor 2036991-001C
C Maintenance
For your notes C-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Maintenance: Assistance and Parts Assistance and Parts If the product malfunctions or if assistance, service, or spare parts are required, contact GE Medical Systems Information Technologies Technical Support. GE Medical Systems Information Technologies provides an assembly exchange service. Before contacting GE Medical Systems Information Technologies, it is helpful for you to duplicate the problem and check and confirm the operation of all accessories to ensure that they are not the cause of the problem.
Maintenance: Maintenance, Calibration, and Cleaning CAUTIONS Never immerse monitor or accessories in any liquid. Do not attach the monitor or accessories to a patient until it is thoroughly dry. WARNING Failure to follow these cleaning recommendations may melt, distort, or dull the finish of displays and cases; blur lettering on labels; embrittle cases and lead to cracks and breakage; or cause equipment failures.
Maintenance: Maintenance, Calibration, and Cleaning Cuff Cleaning and Disinfection 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. Apply cuff hose caps before cleaning. The following cleansing procedure was repeated 20 times on DURA-CUF Blood Pressure Cuffs and once on SOFT-CUF Blood Pressure Cuffs without affecting the performance of the cuff.
Maintenance: Battery and Storage Care Temperature Devices Do not immerse predictive temperature probes. The probe may be cleaned with a solution of 10% bleach in water. Use a cloth or sponge—just damp, not wet— and avoid getting any liquid into the interior of the probe. SpO2 Sensors Adhesive sensors are sterile and for single use only. Reusable sensors should be cleaned before reuse with a 70% alcohol solution. If low-level disinfection is required, use a 1:10 bleach solution.
Maintenance: Battery and Storage Care CAUTIONS To ensure that the battery will be ready for portable operation, keep the monitor connected to a mains supply whenever possible. Repeated failure to fully charge the battery will result in a significant reduction in battery life. The expected lifetime of the battery largely depends on the way in which the monitor is used.
Maintenance: Repairs 5. Insert the battery into the compartment. 6. Then 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. NOTE: 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. 7. Reset the date/time and applicable user settings.
Maintenance: Packaging Material Packaging Material Retain original packaging materials for future use in storing or shipping the monitor and accessories. This recommendation includes corrugated shippers and foam/corrugated spacers. Whenever possible recycle the packaging of accessories and patient applied parts.
Maintenance: Disposal of Product Waste Monitor At the end of its service life, the product described in this manual, as well as its accessories, must be disposed of in compliance with the guidelines regulating the disposal of such products. If you have questions concerning disposal of the product, please contact GE Medical Systems Information Technologies or its representatives. As you use the V100 Vital Signs Monitor, you will accumulate solid wastes that require proper disposal or recycling.
D Principles of Noninvasive Blood Pressure Determination
For your notes D-2 CARESCAPE V100 Vital Signs Monitor 2036991-001C
Principles of Noninvasive Blood Pressure Determination: DINAMAP SuperSTAT Algorithm DINAMAP SuperSTAT Algorithm The oscillometric method of determining NIBP is accomplished by a sensitive transducer which measures cuff pressure and pressure oscillations within the cuff. For the first determination taken on a patient, the algorithm stores the pattern of the patient's oscillation size as a function of the pressure steps.
Principles of Noninvasive Blood Pressure Determination: DINAMAP SuperSTAT Algorithm 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 for an NIBP determination.
Principles of Noninvasive Blood Pressure Determination: DINAMAP Classic and Auscultatory Reference Algorithm DINAMAP Classic and Auscultatory Reference Algorithm The oscillometric method of determining NIBP is accomplished by a sensitive transducer, which measures cuff pressure and minute pressure oscillations within the cuff.
Principles of Noninvasive Blood Pressure Determination: DINAMAP Classic and Auscultatory Reference Algorithm 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.
Principles of Noninvasive Blood Pressure Determination: DINAMAP Classic and Auscultatory Reference Algorithm CARESCAPE V100 Monitors With Intra-Arterial Reference (DINAMAP SuperSTAT and Classic Technology) For these monitors, the NIBP is referenced to the invasive blood pressure obtained at the central aortic region.
Principles of Noninvasive Blood Pressure Determination: DINAMAP Classic and Auscultatory Reference Algorithm D-8 CARESCAPE V100 Vital Signs Monitor 2036991-001C
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