Innovo® CMS 50F PLUS User Manual
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High priority alarm indicates that immediate operator
response is required.
6.2 Cautions
A.
Please check device before use to confirm that it is working
normally. The SpO
2
and PR should be displayed correctly on the
screen.
B.
The finger should be place in between the LED lights and
the sensor (see Figure 1 and 5 for reference), or it may result in
inaccurate measurement.
C.
The SpO
2
sensor should not be used on an arm with a blood
pressure cuff or undergoing intravenous injection. It should not be
used on the arterial canal too.
D.
Do not fix the SpO
2
sensor with adhesive as it might lead to
inaccurate measurement of the SpO
2
and pulse rate.
E.
Excessive ambient light may affect measuring result
although the Acc U Rate
®
SnugFit probe is designed to minimize
such interference. Ambience light includes, but is not limited to
fluorescent lamp, dual ruby light, infrared heater, direct sunlight
and LED lights.
F.
Strenuous activities or extreme electrosurgical interference
may affect accuracy pf device.
G.
User should not use enamel or other makeup to ensure
accuracy.
H.
Please clean and disinfect the device according to
instructions outlined in Chapter 7.1 of the user manual.
6.3 Clinical Restrictions
A.
As the accuracy of the device is based on the arteriole blood,
an adequate amount of blood flow is required. The SpO
2
waveform (Plethysmography) will decrease for users with a weak
