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Figure 1. Operating Principle
3.2 Caution
1. The nger should be placed properly (see the attached
illustration of this manual, Figure 5), or else it may cause
inaccurate measurement.
2. The SpO2 sensor and photoelectric receiving tube
should be arranged in a way with the subject’s arteriole
in a position there between.
3. The SpO2 sensor should not be used at a location
or limb tied with arterial canal or blood pressure cuff or
receiving intravenous injection.
4. Make sure the optical path is free from any optical obsta-
cles like rubberized fabric.
5. Excessive ambient light may affect the measuring result.
It includes uorescent lamp, dual ruby light, infrared
heater, direct sunlight and etc.
6. Strenuous action of the subject or extreme electrosurgi-
cal interference may also affect the accuracy.
7. Testee can not use enamel or other makeup.
3.3 Clinical Restrictions
1. As the measure is taken on the basis of arteriole pulse,
substantial pulsating blood ow of subject is required.
For a subject with weak pulse due to shock, low ambi-
ent/body temperature, major bleeding, or use of vascu-
lar contracting drug, the SpO2 waveform (PLETH) will
decrease. In this case, the measurement will be more
sensitive to interference.
Glow and Infrared-ray
Emission Tube
Glow and Infrared-ray
Receipt Tube
ENGLISH
8


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