Specifications; Intended Use - Philips IntelliVue CL SpO2 Instructions For Use Manual

Specifications

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The specifications in this section apply to the:
• IntelliVue CL SpO
• IntelliVue CL NBP Pod
• IntelliVue CL Charging Station
• IntelliVue CL Transmitter
• IntelliVue CL Transmitter Base Station
• IntelliVue CL Hotspot
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. hyperbaric chambers). During MR imaging, remove all
IntelliVue Cableless Measurement Devices and sensors from the patient. Induced currents could cause
burns.

Intended Use

IntelliVue CL SpO2 Pod:
The IntelliVue CL SpO
for acquisition or monitoring of physiological patient parameters SpO
The intended use of the IntelliVue CL SpO
telemetry system transceiver is for monitoring and recording of and to generate alarms for arterial
oxygen saturation and pulse rate of adult and pediatric patients.
The IntelliVue CL SpO
rate data of adult and pediatric patients for a clinical information management system.
The IntelliVue CL SpO
intended for home use. It is not a therapeutic device.
Pod
2
Pod is indicated for use by health care professionals whenever there is a need
2
Pod when used together with a patient monitor or with a
2
Pod is also intended for acquisition of arterial oxygen saturation and pulse
2
Pod is intended for use by health care professionals inside hospitals. It is not
2
and pulse rate wirelessly.
2
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