PULOX PO-100 Manual De Instrucciones página 31

Infrared light
Safety class
International
Protection
Working voltage
Working current
Power supply
Battery life
Dimensions and Weight
Dimension
Weight
Note 1: the claims of SpO2 accuracy shall be supported by clinical study
measurements taken over the full range. By artificial inducing, get the stable
oxygen level to the range of 70 % to 100 % SpO2, compare the SpO2 values
collected by the secondary standard pulse oximeter equipment and the
tested equipment at the same time, to form paired data, which are used for
the accuracy analysis.
There are 12 healthy volunteers (male: 6. female: 6; age: 18~45; skin color:
black: 2, light: 8, white: 2) data in the clinical report.
Note 2: because pulse oximeter equipment measurements are statistically
distributed, only about two-thirds of pulse oximeter equipment
measurements can be expected to fall within ±Arms of the value measured
by a CO-OXIMETER.
Note 3: percentage modulation of infrared signal as the indication of
pulsating signal strength, patient simulator has been used to verify its
accuracy under conditions of low perfusion. SpO
due to low signal conditions, compare them with the known SpO
values of input signal.
Note 4: optical sensors as the light-emitting components, will affect other
medical devices applied the wavelength range. The information may be
useful for the clinicians who carry out the optical treatment.For example,
photodynamic therapy operated by clinician.
Note 5: Patient simulator has been used to verify the pulse rate accuracy, it
is stated as the root-mean-square difference between the PR measurement
Wavelength: about 905 nm, optical output
power: < 6.75 mW
Internally powered equipment, type BF applied
part
IP22
DC 2.6 V ~ 3.6 V
≤ 25 mA
1.5V (AAA size) alkaline batteries × 2 or
rechargeable battery
Two batteries can work continually for 24 hours
57(L) × 31(W) × 32 (H) mm
About 50g (with the batteries)
and PR values are different
2
EN
and PR
2