User's Manual
Table Of Contents
- Instructions for Use
- 1 Introduction and Basic Operation 7
- 2 Monitoring with the IntelliVue Cableless Measurements 19
- 3 Monitoring SpO2 25
- 4 Monitoring NBP 33
- 5 Technical Alarms (INOPs) 41
- 6 Care and Cleaning 47
- 7 Maintenance and Troubleshooting 51
- 8 Integrated Battery Handling 53
- 9 Accessories 55
- 10 Specifications 59
- Index 73
- Introduction and Basic Operation
- Introducing the IntelliVue Cableless Measurements
- Operating and Navigating
- Switching the Devices On and Off
- Screen Layout
- Standard Layout
- 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.
- 3 Battery indicator
- 4 Measurement values
- 5 Measurement-related symbols (see the measurement chapters for details)
- 6 Patient identification (from a monitor or telemetry device)
- 1 Connection status indicator
- 2 Battery indicator
- 3 Measurement values
- 4 Measurement-related symbols (see the measurement chapters for details) The Alarms Off symbols indicate that no physiological alarms are available from the Cableless Measurement Devices when not assigned to a host.
- 5 Patient identification (from a monitor or telemetry device)
- INOP Layout
- Low-Activity Screen
- Standard Layout
- When a Cableless Measurement Device Cannot be Activated
- Using the Hard Keys
- Using the SmartKeys
- Using the Main Setup Menu
- Operating Modes
- Using the Patient Menu
- Using Profiles
- Setting the Date and Time
- Charging IntelliVue Cableless Measurement Devices
- Monitoring with the IntelliVue Cableless Measurements
- Monitoring SpO2
- NOTE
- SpO2 Sensors
- 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
- Removing the Pod from the Cradle
- 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...
- 2 Remove colored nail polish from the application site.
- 3 Apply the sensor to the patient. The application site should match the sensor size so that the sensor can neither fall off, nor apply excessive pressure. See the sections below for details on applying the different sensors.
- 4 Check that the light emitter and the photodetector are directly opposite each other. All light from the emitter must pass through the patient's tissue.
- WARNING
- Measuring SpO2
- Selecting Measurement Modes
- Understanding SpO2 Numerics and Symbols
- Assessing a Suspicious SpO2 Reading
- Changing the Averaging Time
- Understanding SpO2 Alarms
- Perfusion Numeric (only available on the Patient Monitor)
- Monitoring NBP
- Introducing the Oscillometric NBP Measurement
- 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...
- 3 Make sure that you are using a Philips-approved correct sized cuff and that the bladder inside the cover is not folded or twisted.
- 4 Apply the cuff to the upper arm at the same level as the heart. If it is not at heart level, you must use the measurement correction formula to correct the measurement.
- CAUTION
- Additional Information
- Using a Carrying Pouch
- 1 Apply the cuff as described in step 4 above.
- 2 Secure the pouch on the patient, with the upper ties around the patient's head and arm and the lower ties around the patient's torso.
- 3 Insert the NBP Pod into the cradle.
- 4 Attach the extension hose to the NBP Pod in the cradle.
- 5 Insert the NBP cradle into the pouch
- 6 Connect the extension hose to the cuff.
- Starting and Stopping Measurements
- Enabling Automatic Mode and Setting Repetition Time
- Enabling Sequence Mode and Setting Up The Sequence
- 1 In the NBP menu, select Mode and select Sequence from the pop-up menu.
- 2 Select Setup Sequence to open the Setup Sequence menu.
- 3 Select each phase in turn (A, B, C and D) and select the number of measurements and the time interval between the measurements.
- 4 To have measurements continue after the sequence, set the number of measurements for your last phase to Cont and this phase will run indefinitely.
- CAUTION
- Understanding the NBP Numerics and Symbols
- Correcting the Measurement if Limb is not at Heart Level
- Switching Pulse from NBP On/Off
- Assisting Venous Puncture
- Calibrating NBP
- Technical Alarms (INOPs)
- Care and Cleaning
- Maintenance and Troubleshooting
- WARNING
- Inspecting the Equipment and Accessories
- 1 Examine unit exteriors for cleanliness and general physical condition. Make sure that the housings are not cracked or broken, that everything is present, that there are no spilled liquids and that there are no signs of abuse.
- 2 Inspect all accessories (cables, sensors and so forth). If any show signs of damage, do not use them.
- WARNING
- Maintenance Task and Test Schedule
- Troubleshooting
- Disposing of the IntelliVue Cableless Measurement Devices
- Integrated Battery Handling
- Accessories
- Specifications
- WARNING
- Intended Use
- Manufacturer's Information
- Symbols
- Installation Safety Information
- Safety Specifications
- EMC And Radio Regulatory Compliance
- IntelliVue CL SpO2 Pod Specifications
- IntelliVue CL NBP Pod Specifications
- Alarm Specifications
- Telemetry Device Battery Runtime Specifications
- IntelliVue CL Charging Station Specifications
- IntelliVue CL Transmitter Base Station Specifications
- Safety and Performance Tests
- Electromagnetic Compatibility (EMC) Specifications
- Accessories Compliant with EMC Standards
- Electrosurgery Interference/Defibrillation
10 Specifications
62
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. Any changes or modifications to this equipment not expressly approved by Philips Medical
Systems may cause harmful radio frequency interference and void your authority to operate this
equipment.
Devices Including the Short Range Radio Interface
Philips Medizin Systeme Boeblingen GmbH hereby declares that the radio component used
in this product is in compliance with the essential requirements and other relevant provisions of
Directive 1999/5/EC (Radio Equipment and Telecommunications Terminal Equipment Directive).
Class 1 radio equipment.
In addition the product complies with: ETSI EN 300 328; AS/NZS 4771+A1; ARIB STD-T66.
To obtain a copy of the original Declaration of Conformity, please contact Philips at the address as
stated in the "Manufacturer's Information" section of these Instructions for Use.
WARNING
• This equipment generates, uses and radiates radio-frequency energy, and if it is not installed and
used in accordance with its accompanying documentation, may cause interference to radio
communications.
• The device, equipped with a wireless network interface, intentionally receives RF electromagnetic
energy for the purpose of its operation. Therefore, other equipment may cause interference, even
if that other equipment complies with CISPR emission requirements.
IntelliVue 802.11 WLAN Adapter
FCC and Industry Canada Radio Compliance: 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. Any changes or modifications to this equipment not
expressly approved by Philips Medical Systems may cause harmful radio frequency interference and
void your authority to operate this equipment.
The maximum antenna gain permitted (for devices in the 5250-5350 MHz and 5470-5725 MHz bands)
complies with the e.i.r.p. limits as stated in RSS-210.
The maximum antenna gain permitted (for devices in the 5725-5825 MHz band) complies with the
e.i.r.p. limits specified for point-to-point operation, as stated in RSS-210.
The device for the band 5150-5250 MHz is only for indoor usage to reduce potential for harmful
interference to co-channel mobile satellite systems.
The OEM radio device used in this product is in compliance with the essential requirements and other
relevant provisions of Directive 1999/5/EC. This product is intended to be connected to the Publicly
Available Interfaces (PAI) and used throughout the EEA.