Covidien Nellcor Series, Operator'S Manual

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4-1
4 Operation
4.1
Overview
This chapter identifies methods for viewing and collecting patient oxygen satura-
tion data using the Nellcor™ bedside SpO
2
patient monitoring system. Before oper-
ating the monitoring system, thoroughly read this manual.
4.2
Safety Reminders

WARNING:
The monitoring system is intended only as an adjunct in patient assessment. It must
be used in conjunction with clinical signs and symptoms.

WARNING:
Tissue damage can be caused by incorrect application or use of a pulse oximetry
sensor. Do not wrap the pulse oximetry sensor too tightly, apply supplemental tape,
or leave it too long on one place. Inspect the pulse oximetry sensor site as directed in
the
Directions for Use to ensure skin integrity, correct positioning, and adhesion.

WARNING:
Keep patients under close surveillance when monitoring. It is possible, although
unlikely, that radiated electromagnetic signals from sources external to the patient
and the monitoring system can cause inaccurate measurement readings. Do not rely
entirely on the monitoring system's readings for patient assessment. This device has
been tested and found to comply with the limits for medical devices related to IEC
60601-1-2: 2007 and IEC 60601-1-2:2014. These limits are designed to provide
reasonable protection against harmful interference in a typical medical installation.

WARNING:
For best product performance and measurement accuracy, use only accessories
supplied or recommended by Covidien. Use accessories according to their respective
Directions for Use .