ft ra D In str uct ion s fo r Use IntelliVue Cableless Measurements IntelliVue CL SpO2 Pod and CL NBP Pod R e l e a s e A .
Part Number 453564199661 Printed in Germany 07/10 *453564199661*
Table of Contents 1 1 Introduction and Basic Operation Introducing the IntelliVue Cableless Measurements Operating and Navigating Operating Modes Using the Patient Menu Using Profiles Setting the Date and Time Charging IntelliVue Cableless Measurement Devices 2 Monitoring with the IntelliVue Cableless Measurements IntelliVue Cableless Measurements Use Models Assigning an IntelliVue Cableless Measurement Device to a Patient Monitor or Telemetry Device Controls Available with a Patient Monitor Controls Ava
5 Technical Alarms (INOPs) 41 Display of INOPs Acknowledging an INOP Displaying a List of Current INOPs Setting the Volume of the INOP Tone Reference List of all INOPs 41 41 41 42 42 6 Care and Cleaning 47 General Points Cleaning and Disinfecting the IntelliVue Cableless Measurements 47 48 7 Maintenance and Troubleshooting 51 Inspecting the Equipment and Accessories Maintenance Task and Test Schedule Troubleshooting Disposing of the IntelliVue Cableless Measurement Devices 51 51 52 52 8 Integrat
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1 Introduction and Basic Operation 1 These Instructions for Use are for clinical professionals using the IntelliVue Cableless Measurements and their respective accessories together with IntelliVue Patient Monitors MP5/MP5T, MP2 or X2 or with the IntelliVue Telemetry System Transceiver TRx4841A/TRx4851A for monitoring and recording arterial oxygen saturation, pulse rate and non-invasive blood pressure of adult and pediatric patients.
1 Introduction and Basic Operation Introducing the IntelliVue Cableless Measurements The IntelliVue Cableless Measurements family consists of the following components and their respective accessories: IntelliVue CL SpO2 Pod IntelliVue CL NBP Pod IntelliVue CL Charging Station The cableless measurement devices provide measurement values on the built-in display and communicate them to other system components using a wireless short range radio (SRR) interface.
1 Introduction and Basic Operation IntelliVue CL SpO2 Pod The IntelliVue CL SpO2 Pod is a battery powered, cableless Pulse Oximetry measuring device. It is a wrist-worn device; you need a Mobile CL SpO2 Cradle to hold the sensor connector in place and a wristband to fix the cradle to a patient's arm. Specialized single-patient SpO2 sensors are available for use with the IntelliVue CL SpO2 Pod.
1 Introduction and Basic Operation If the ambient temperature is high, the built-in fan will switch on automatically to cool the charging station. WARNING Ensure that the charging station does not come into close contact with implanted pacemakers, to avoid magnetic interference affecting the mode of the pacemaker. CAUTION The charging station generates a magnetic field.
1 Introduction and Basic Operation Measurement Device Main Parts and Keys All IntelliVue Cableless Measurement devices have an integrated monochrome LCD display and 3 keys. 1 Integrated monochrome LCD display 2 Hard keys: ◄, 9, ► 3 Measurement identifier Operating and Navigating The following sections describe operation on the IntelliVue Cableless Measurement device itself.
1 Introduction and Basic Operation Standard Layout When assigned to a monitor or telemetry device: 1 Connection status indicator 2 Indicator that alarming capability has been transferred to the host (to the monitor or, for the telemetry device, to the Information Center). No patient alarms will be announced on the Cableless Measurement Device.
1 Introduction and Basic Operation Low-Activity Screen If the measurement device has not been operated for a while, the screen lighting will switch itself off and a little later the screen will switch to a pre-configured "low-activity" screen. When a Cableless Measurement Device Cannot be Activated If you cannot activate a device by pressing a key, the battery in the device may have been empty for an extended period of time.
1 Introduction and Basic Operation Use the ◄ and ► hardkeys to move along the row of SmartKeys. The highlighted SmartKey is displayed in full above the row of SmartKeys. When you use the ◄ or ► hardkey at the end of the row, an Exit screen appears and then with further presses you move on to the next page of SmartKeys. To leave the SmartKeys menu you can use the Exit screen or press the ► hardkey for a couple of seconds to return to the Main Screen.
1 Introduction and Basic Operation SmartKey Text Labels change Screen enter Profiles menu switch device off enter Patient menu Using the Main Setup Menu In addition to the hard keys and SmartKeys for the most needed functions, the Main Setup menu gets you to all settings that can be adjusted for the respective device. Select the Main Setup SmartKey to get to the Main Setup menu.
1 Introduction and Basic Operation • Demonstration Mode: Passcode protected, this is for demonstration purposes only. You must not change into Demonstration Mode during monitoring. • Configuration Mode: Passcode protected, this mode is for personnel trained in configuration tasks. These tasks are described in the Configuration Guide. During installation the Cableless Measurement Device is configured for use in your environment.
1 Introduction and Basic Operation Using Profiles A profile is a set of measurement and general settings which have been customized for a particular purpose. The Cableless Measurement Devices can have four different profiles configured to your requirements. The default profile is marked with a symbol. To select a different profile, 1 Select the Profiles SmartKey or the Main Setup SmartKey followed by Profiles. 2 Select the required profile from the list.
1 Introduction and Basic Operation • battery status information on both the device's and the charging station's display • INOP messages • battery icon on the patient monitor's screen (when assigned to a patient monitor) The indicators always show the remaining capacity in relation to the battery's actual maximum capacity, which may lessen as the battery ages. You can see the actual capacity in the Battery menu.
2 Monitoring with the IntelliVue Cableless Measurements 2 IntelliVue Cableless Measurements Use Models With these patient-worn measurement devices you can measure and transmit a patient's vitals regularly or on an intermittent data collection basis. There are two typical use models: With a Patient Monitor The SpO2 and the NBP Pods can be used together with an MP5/MP5T, MP2 or X2 patient monitor (with a SRR interface). They can communicate their measurement values via short range radio to the monitor.
2 Monitoring with the IntelliVue Cableless Measurements When a cableless measurement device is assigned to a telemetry device, it is not possible for the telemetry device to be wirelessly assigned or directly connected to a patient monitor. If the connection between the telemetry device and the NBP Pod or SpO2 Pod is lost, an INOP will be displayed at the Information Center: cl SpO₂ Disconnect or cl NBP Disconnect. A No System Monitor. INOP will be displayed on the Pod.
2 Monitoring with the IntelliVue Cableless Measurements A telemetry device must be put into assignment mode by pressing the 9 key on the telemetry device before it can appear in the list. Pressing the 9 key starts an SRR channel search to find the clearest channel available. During the search all 4 LEDs flash once per second. The search will take approximately 20-25 seconds.
2 Monitoring with the IntelliVue Cableless Measurements When the cableless measurement device is assigned, the symbol appears on its display indicating that alarms from the device will be sent to the patient monitor. An assigned cableless measurement device can be removed in the Measurement Selection window. For more details see the Instructions for Use for your patient monitor.
2 Monitoring with the IntelliVue Cableless Measurements WARNING If a patient being monitored by Cableless Measurement Devices moves out of range of the patient monitor, the measurements are available on the Cableless Measurement Device only. They are not transmitted to the patient monitor or the Information Center. If this occurs, the No Host Monitoring message is displayed on the measurement device. The measurement device will also sound the INOP tone.
2 Monitoring with the IntelliVue Cableless Measurements NOTE When you unplug the ECG cable from the telemetry device and plug it into the monitor associated with the same patient, the ECG source will automatically be from the monitor. The SpO2 and/or NBP measurement devices assigned to the telemetry device will continue to source data to the telemetry device and the Information Center. You may need to change screens on the patient monitor to see the measurements.
3 3 Monitoring SpO2 Philips pulse oximetry uses a motion-tolerant signal processing algorithm, based on Fourier artifact suppression technology (FAST). A sensor is used that transmits light of two different wavelengths through the tissue of the patient. The measurement principle of pulse oximetry is based on the specific absorption characteristics of oxyhemoglobin and deoxyhemoglobin and the pulsating arteriolar vascular bed at the measurement site.
3 Monitoring SpO2 Connecting SpO2 Sensors 1 Connect the sensor to the single patient Mobile CL SpO2 Cradle (if not already connected). 2 Insert the SpO2 Pod into the Mobile CL SpO2 Cradle. The correct orientation is indicated by a matching blue dot inside the cradle. CAUTION Make sure that the contacts of the SpO2 Pod and the sensor are dry and free of residues. 3 Secure the cradle on the patient's arm using the wristband. a.
3 Monitoring SpO2 Removing the Pod from the Cradle To remove the SpO2 Pod from the cradle, pull on the Pod at the opening in the cradle, while holding the cradle in place on the patient's arm. Applying the Sensor 1 Choose a finger of the patient that matches the sensor dimension in a way that the sensor optical components are properly aligned and the sensor is neither too loose nor applies too much pressure to the finger. For small pediatric patients consider the thumb.
3 Monitoring SpO2 Extremities to Avoid: Avoid placing the sensor on extremities with an arterial catheter, an NBP cuff or an intravascular venous infusion line. Measuring SpO2 During measurement, ensure that the application site: – – has a pulsatile flow, ideally with a perfusion indicator value above 1.0 or, if the perfusion indicator is not available, with signal quality indicator of at least medium. has not changed in its thickness (for example, due to edema), causing an improper fit of the sensor.
3 Monitoring SpO2 • Continuous mode - SpO2 is measured continuously until the measurement is switched off. • Manual mode - a single SpO2 measurement is made when the Start SpO₂ SmartKey or the Start SpO₂ menu item is selected. One set of values is then displayed with the time the measurement was made. • Automatic mode - a series of measurements is made with an interval between them. The interval is selected using the Repeat Time SmartKey or the Repeat menu item.
3 Monitoring SpO2 Assessing a Suspicious SpO2 Reading Traditionally, pulse rate from SpO2 was compared with heart rate from ECG to confirm the validity of the SpO2 reading. With newer algorithms, such as FAST-SpO2, this is no longer a valid criteria because the correct calculation of SpO2 is not directly linked to the correct detection of each pulse.
3 Monitoring SpO2 • The time between the displayed numerical values crossing an alarm limit and the alarm indication on the monitor. This delay depends on the host system. Refer to the Instructions for Use of the monitor for information about the SpO2 and pulse rate alarms. Perfusion Numeric (only available on the Patient Monitor) The perfusion numeric (Perf) gives a value for the pulsatile portion of the measured signal caused by the pulsating arterial blood flow.
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4 4 Monitoring NBP The IntelliVue CL NBP Pod uses the oscillometric method for measuring NBP. The blood pressure measurements determined with this device comply with the American National Standard for Electronic or Automated Sphygmomanometers (ANSI/AAMI SP10:2002/(R)2008 + A1:2003/ (R)2008) in relation to mean error and standard deviation, when compared to auscultatory measurements (depending on the configuration) in a representative patient population.
4 Monitoring NBP Unattended measurement: Use clinical judgement to decide whether to perform frequent unattended blood pressure measurements in cases of severe blood clotting disorders because of the risk of hematoma in the limb fitted with the cuff. CAUTION If you spill liquid onto the equipment or accessories, particularly if there is a chance that it can get inside the tubing or the measurement device, contact your service personnel.
4 Monitoring NBP Preparing to Measure NBP 1 Attach the cradle to the NBP cuff and insert the NBP Pod into the cradle. 2 Plug the air tubing into the NBP Pod. Hold the flat part of the connector vertically when plugging it into the inlet, then twist it clockwise to lock into place. Avoid compression or restriction of pressure tubes. Air must pass unrestricted through the tubing.
4 Monitoring NBP • Mobile CL Single-Patient NBP Cuffs Instructions for Use • Mobile CL NBP Cradle Instructions for Use • Mobile CL Extension Air Hose Instructions for Use Using a Carrying Pouch As an alternative to fixing the NBP Pod on the cuff, you can insert it in a telemetry pouch which can be worn. In this case the NBP Pod is connected via an extension hose to the cuff. 1 Apply the cuff as described in step 4 above.
4 Monitoring NBP CAUTION Use clinical judgment to decide whether to perform repeated series of STAT measurements because of the risk of purpura, ischemia and neuropathy in the limb with the cuff. Enabling Automatic Mode and Setting Repetition Time 1 In the NBP menu, select Mode and select Auto from the pop-up menu. 2 For an automatic measurement, select Repeat and set the time interval between two measurements.
4 Monitoring NBP Understanding the NBP Numerics and Symbols 1 Systolic/Diastolic pressure 2 Mean pressure 3 Pulse rate 4 Pulse rate indicator 5 Measurement mode (see below) 6 Alarms Off symbol for Pulse 7 Timestamp 8 Alarms Off symbol for NBP Note: The Alarms Off symbols indicate that no physiological alarms are available on the Cableless Measurement Devices when not assigned to a host.
4 Monitoring NBP • In the NBP menu select Pulse. Assisting Venous Puncture You can use the NBP cuff to cause sub-diastolic pressure. The cuff deflates automatically after a set time (adult/pediatric 170 seconds) if you do not deflate it. 1 In the NBP menu select Veni Puncture, or select the Veni Puncture SmartKey. 2 Puncture vein and draw blood sample. 3 Reselect Veni Puncture to deflate the cuff.
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5 Technical Alarms (INOPs) 5 Technical alarms, also known as INOPs, indicate that the measuring device cannot measure reliably. If an INOP interrupts monitoring (for example, NBP INTERRUPTED), there will be a question mark in place of the measurement numeric. An INOP tone sounds at the Cableless Measurement Device only when there is no SRR connection to a monitor. Some INOPs have a severity indication: !! for a medium severity INOP and !!! for a high severity INOP.
5 Technical Alarms (INOPs) Setting the Volume of the INOP Tone To set the volume for the INOP tone, 1 Select the Main Setup SmartKey. 2 Select INOPs. 3 Select Inop Vol and select a volume setting.The maximum is 10 and the minimum depends on your configuration. Reference List of all INOPs INOP Message, Indication Source What to do Batt Incompatible Battery Battery cannot be used with this Cableless Measurement Device.
5 Technical Alarms (INOPs) INOP Message, Indication Source What to do cl NBP Disconnect Cableless at Information Center or at patient Measurement Device monitor The NBP Pod has lost the SRR connection to the telemetry device or the patient monitor. cl SpO₂ Disconnect Cableless at Information Center or at patient Measurement Device monitor The SpO2 Pod has lost the SRR connection to the telemetry device or the patient monitor.
5 Technical Alarms (INOPs) INOP Message, Indication Source What to do NBP Neo Patient? NBP The patient monitor that the NBP pod is assigned to is in neonatal mode or a neonatal cuff has been detected. The monitor must be in adult or pediatric mode. NBP The NBP Pod is not in the cradle. You can silence this INOP, but the INOP message remains visible until the NBP Pod is inserted into the cradle and the next measurement is started or the Stop All SmartKey is selected.
5 Technical Alarms (INOPs) INOP Message, Indication Source What to do NO SENSOR SpO2 Make sure the SpO2 sensor is connected. If the INOP persists, try another sensor. If you acknowledge this INOP, the measurement will be switched off. NOISY SIGN. SpO2 Excessive patient movement or electrical interference is causing irregular pulse patterns. Try to reduce patient movement or to relieve the cable strain on the sensor. NON-PULSAT.
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6 Care and Cleaning 6 Use only the Philips-approved substances and methods listed in this chapter to clean or disinfect your equipment. Warranty does not cover damage caused by using unapproved substances or methods. Philips makes no claims regarding the efficacy of the listed chemicals or methods as a means for controlling infection. Consult your hospital’s Infection Control Officer or Epidemiologist.
6 Care and Cleaning Cleaning and Disinfecting the IntelliVue Cableless Measurements The following instructions apply to the IntelliVue CL SpO2 Pod, the IntelliVue CL NBP Pod, the corresponding single patient Mobile CL Cradles and the IntelliVue CL Charging Station. Clean with a lint-free cloth, moistened with warm water (40°C/104°F maximum) and soap, a diluted non-caustic detergent, tenside, ammonia- or alcohol-based cleaning agent. Do not use strong solvents such as acetone or trichloroethylene.
6 Care and Cleaning Product Name Product Type Ingredients spray 0.5% accelerated hydrogen peroxide Carpe DiemTM/MC Tb Wipes wipes 0.5% accelerated hydrogen peroxide Super Sani-Cloth wipes isopropanol 55% quaternary ammonium chlorides 0.5% wipes isopropanol 15% quaternary ammonium chlorides 0.25% wipes isopropanol < 0.15% quaternary ammonium chlorides 0.
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7 Maintenance and Troubleshooting 7 WARNING Schedule: Failure on the part of the responsible individual hospital or institution employing the use of this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards. Contact: If you discover a problem with any of the equipment, contact your service personnel, Philips, or your authorized supplier.
7 Maintenance and Troubleshooting Ensure that these tasks are carried out as indicated by the device's maintenance schedule, or as specified by local laws. Contact a Philips-qualified service provider if your device needs a safety or performance test. Clean and disinfect equipment to decontaminate it before testing or maintaining it. Troubleshooting If a device will not switch on when you press a key, place it onto a charger slot on the charging station.
8 8 Integrated Battery Handling Battery Care Battery care begins when you receive a new IntelliVue Cableless Measurement Device with built-in battery and continues throughout the life of the device. The table below lists battery care activities and when they should be performed. Activity When to perform Perform a visual inspection Before using the IntelliVue Cableless Measurement Device Charge the battery Upon receipt, after use, or if a low battery state is indicated.
8 Integrated Battery Handling Storage If unused IntelliVue Cableless Measurement Devices are stored for an extended period of time: • they should be powered off for storage • they should be stored in a cool place, ideally between 15°C and 25°C (60°F and 77°F) • the state of charge should be between 40 and 50% • they should be recharged every six months Storing in a cool place slows the aging process of the batteries. They should be fully charged prior to use.
9 Accessories 9 You can order parts and accessories from Philips supplies at www.medical.philips.com or consult your local Philips representative for details. WARNING Reuse: Never reuse single-patient sensors, accessories and so forth that are intended for single use, or single patient use only. Reuse may compromise device functionality and system performance and cause a potential hazard, in particular with regard to cross-contamination. Philips’ approval: Use only Philips-approved accessories.
9 Accessories Order Number Description Contents 9898031659311 Mobile CL reusable SpO2 sensor and Cradles for use on pediatric and adult patients >15kg 1 Reusable Mobile CL RSpO2-1A Sensor 20 Single-Patient Cradles with preattached Wristbands 989803165951 Mobile CL 20 SpO2 Cradles (single patient) 20 Single-Patient Cradles with preattached Wristbands 989803165961 Mobile CL 50 SpO2 Wristbands (single 50 Single-Patient Wristbands patient) 989803168861 Mobile CL SpO2 Battery Kit 1 1 Battery 1 disa
9 Accessories Order Number Description Limb Circumference Range Bladder Width Contents 989803137831 Telemetry Pouch with window - - 50 pouches 989803140371 Telemetry Pouch with window - - 4 boxes of 50 pouches 989803101971 White Telemetry Pouch with Snaps; box of 50. - - 50 pouches White Telemetry Pouch with Snaps; 4 boxes of 50.
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10 10 Specifications The specifications in this section apply to the IntelliVue CL SpO2 Pod, the IntelliVue CL NBP Pod, IntelliVue CL Charging Station and the IntelliVue CL Transmitter. The IntelliVue Cableless Measurements might not meet the performance specification listed in this chapter, if stored or operated outside the specified environmental conditions. WARNING The IntelliVue Cableless Measurement Devices are not intended for use in an MRI environment or in an oxygen-enriched environment (e.g.
10 Specifications Philips Medizin Systeme Boeblingen GmbH Hewlett-Packard-Str. 2 71034 Boeblingen Germany Visit our website at: www.healthcare.philips.com/us/. © Copyright 2010. Koninklijke Philips Electronics N.V. All Rights Reserved. Symbols These symbols can appear on the cableless measurement devices and associated equipment.
10 Specifications Installation Safety Information Grounding The charging station must be grounded during operation. If a three-wire receptacle is not available, consult the hospital electrician. Never use a three-wire to two-wire adapter. Equipotential Grounding If the charging station is used in an OR, ensure that the room incorporates an equipotential grounding system to which the charger has a connection.
10 Specifications This device complies with Part 15 of the FCC Rules and RSS-210 of Industry Canada. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.
10 Specifications CAUTION High power radars are allocated as primary users (meaning they have priority) of 5250-5350 MHz and 5650-5850 MHz and these radars could cause interference and /or damage to LE-LAN devices. IntelliVue 802.
10 Specifications Environmental Specifications Operating Temperature Range 0 to 40°C (32 to 104°F) Operating Humidity Range ≤95% RH @ 40°C (104°F) Operating Altitude Range -500 to 3000 m Storage/Transportation Temperature Range -20 to 60°C (-4 to 140°F) Storage/Transportation Humidity Range ≤90% RH @ 60°C (140°F) no condensation Storage/Transportation Altitude Range -500 to 4600 m Measurement Validation: The SpO2 accuracy has been validated in human studies against arterial blood sample reference
10 Specifications Performance Specifications Viewing Area 25.6 mm x 19.2 mm Dot Size 0.2 mm x 0.2 mm Resolution 128 x 96 pixel Backlight white LED Sounds Hardkey operation tone INOP tone Battery Integrated rechargeable Li-Ion battery with battery gauge and cycle counter Runtime (fully charged battery) Continuous measurement: Typically 24 hours Minimum 12 hours Intermittent measurement: Typically > 32 hours with repetition interval of 2.5 minutes Charging Time max 2.
10 Specifications NOTE The effectiveness of this sphygmomanometer has not been established in pregnant, including preeclamptic patients. Physical Specifications Size (H x W x D) 138 x 65 x 30.
10 Specifications IntelliVue CL NBP Pod Performance Specifications Runtime (fully charged battery) Minimum 8 hours @ 4 measurements per hour Typical 24 hours @ 2 measurements per hour Battery Recharge Time Maximum 2.5 hours Short Range Radio Specifications Type built in interface with integrated antenna Technology IEEE 802.15.4 Frequency band 2.4 GHz ISM (2.400 - 2.483 GHz) Modulation DSSS (O-QPSK) Receiver bandwidth 5 MHz Effective radiated power (ERP) max.
10 Specifications IntelliVue CL NBP Pod Performance Specifications Measurement Time Auto/manual/sequence mode: Typical 40 seconds @ >60 bpm and normal adult cuff Maximum 180 seconds STAT Mode: Typical 30 seconds @ >60 bpm and normal adult cuff Maximum 180 seconds STAT Mode Cycle Time 5 minutes Initial Cuff Inflation Pressure Adult: 165 ±15 mmHg Pediatric: 130 ±15 mmHg Venipuncture Pressure Range Adult: 20 to 120 mmHg in steps of 5 mmHg Pediatric: 20 to 80 mmHg in steps of 5 mmHg Venipuncture Pressu
10 Specifications Telemetry Device Battery Runtime Specifications Operating Mode Battery Runtime ECG Only Telemetry Device with CL SpO2/NBP Pod connected 20 hours Telemetry Device is host to CL SpO2/NBP Pod ECG/SpO2 (continuous) Telemetry Device with internal SpO2 running in continuous mode and CL SpO2/NBP Pod connected 8 hours Telemetry Device is host to CL SpO2/NBP Pod IntelliVue CL Charging Station Specifications The IntelliVue CL Charging Station is intended for recharging and performing battery
10 Specifications Performance Specifications Display Specifications Type monochrome (4 grey scales), passive LCD (STN), positive/transflective Viewing Area 25.6 mm x 19.2 mm Dot Size 0.2 mm x 0.2 mm Resolution 128 x 96 pixel Backlight white LED Sounds Hardkey operation tone Charging Current (all slots) max. 4.8A (24W @5V) Charging Current (one slot) max. 2A (10W @ 5V) Mains Power 50/60 Hz; 1.3 - 0.7A; 100 - 240V~ USB Downstream Standard: USB 2.
10 Specifications Environmental Specifications Operating Temperature Range 0 to 40°C (32 to 104°F) Operating Humidity Range ≤95% RH @ 40°C (104°F) Operating Altitude Range -500 to 3000 m Storage/Transportation Temperature Range -20 to 60°C (-4 to 140°F) Storage/Transportation Humidity Range ≤90% RH @ 60°C (140°F) no condensation Storage/Transportation Altitude Range -500 to 4600 m Performance Specifications Charging Interface (output) Power output (PoE powered) 5V ±10% Power output (USB power
10 Specifications Safety and Performance Tests You must observe any national regulations on the qualification of the testing personnel and suitable measuring and testing facilities. See the maintenance section for a list of required tests. Safety and performance tests, and what to do if the instrument does not meet these specifications, are described in the IntelliVue Cableless Measurements Service Guide.
Index 1 A Accessories 55 Accessories Compliant with EMC Standards 72 Acknowledging an INOP 41 Adding a New Patient to the Device 16 Additional Information 25, 35 Alarm Specifications 68 Applying the Sensor 27 Assessing a Suspicious SpO2 Reading 30 Assigning an IntelliVue Cableless Measurement Device to a Patient Monitor or Telemetry Device 20 Assignment at the Measurement Device 20 Assignment at the Patient Monitor 21 Assisting Venous Puncture 39 Availability of Patient Alarms 10 B Battery Care 53 Batter
Removing the Pod from the Cradle 27 S Safety and Performance Tests 72 Safety Specifications 61 Screen Layout 11 Selecting Measurement Modes 28 Setting the Date and Time 17 Setting the Volume of the INOP Tone 42 Smart Keys Menu 13 Specifications 59 SpO2 Sensors 25 SpO2 Signal Quality Indicator 29 Standard Layout 12 Standby Mode 16 Starting and Stopping Measurements 36 Storage 54 Switching Pulse from NBP On/Off 38 Switching the Devices On and Off 11 Symbols 60 T Technical Alarms (INOPs) 41 Telemetry Device
