CONTEC FDA CMS50F Wrist Watch,Pulse Rate,Oximeter,PR Blood Oxygen spo2 probe

Description

CMS50F Pulse Oximeter
Introduction
CMS50F Pulse Oximeter adopts Photoelectric Oxyhemoglobin Inspection Technology integrated with Capacity Pulse Scanning & Recording Technology, which can be used to measure human oxygen saturation and pulse rate through finger. The device is suitable for use in family, hospital, oxygen bar, community healthcare and physical care in sports, etc. (It can be used before or after exercise, but not recommended to use during exercising).
Function
1)Display of SpO2 value.
2)Display of pulse rate and bar graph.
3)Display of pulse waveform.
4)Low-voltage indication: the low power indication symbol appears when the voltage is too low to work.
5)Adjustable screen brightness.
6)PR sound indication.
7)Sound prompt function: over-limit prompt of measured value, probe-off or finger-out prompt, low power prompt.
8)Data memory function.
9)The data can be uploaded to the terminal equipment by wired mode.
11)Clock function.
12)Charging function.
Performance
SpO2 measurement range: 0 % ~ 100 % (resolution: 1 %)
Accuracy: 70 % ~ 100 %, ± 2 %;
0 %~69 %, unspecified
PR measurement range: 30 bpm ~ 250 bpm (resolution: 1 bpm)
Accuracy: ± 2 bpm or ± 2 %, whichever is greater
Accuracy under low perfusion: low perfusion 0.4%, SpO2 accuracy: ± 4 %; PR accuracy: ± 2 bpm or ± 2 %, whichever is greater.
Light interference: compared to the values measured in normal condition and ambient light condition, the deviation is less than ± 1 %.
Power consumption: ≤ 100 mA
Working voltage: DC 3.6 V ~ 4.2 V
Battery: one 3.7 V rechargeable lithium battery
Battery lifetime: ≥ 500 times (charge and discharge times)
Safety class: internally powered equipment, type BF applied part
Accessories
One SpO2 probe
One USB data line
One User Manual
Physical characteristic
Dimension: 61 mm (L) × 56 mm (W) × 24 mm (H)
Weight: about 60 g (including one lithium battery)
Certification
CE, FDA.
The Fingertip PulseOximeter is registered on theAustralian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE &TUV of Europe.