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frequently with some patients. If skin integrity changes,
move the sensor to another site.
29 Do not use supplemental tape to adhere the clip and
sensor directly to the site, this can restrict blood flow
and cause inaccurate measurements.
30 Intravascular
measurements.
31 Performance of the sensor may be compromised by
motion, particularly of a repetitive nature. If readings
cannot be obtained, try another application site.
32 Do not alter or modify the sensor. Alterations or
modifications may affect performance or accuracy.
33 Failure to apply the sensor properly may cause incorrect
measurements.
34 Using the sensor in the presence of bright lights may
result in inaccurate measurements. In such case, cover
the sensor with an opaque material.
35 This equipment is not intended for family usage.

1.2 Cautions

Cautions alert the user to exercise care necessary for the
safe and effective use of the oximeter.
1
All combinations of equipment must be in compliance
with IEC/EN Standard 60601-1-1 systems requirements.
2
The device and accessories are to be disposed of
according to local regulations after their useful lives.
Alternatively, they can be returned to the dealer or the
manufacturer for recycling or proper disposal. Batteries
are hazardous waste. Do NOT dispose them together
with house-hold garbage. At the end of their life hand
the batteries over to the applicable collection points for
the recycling of waste batteries. For more detailed
dyes
may
CAUTION
9
lead
to
inaccurate

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