Pulse oximeters give an estimated oxygen saturation level value. Several research studies and an FDA 2021 safety communication have found that certain physical traits, including but not limited to darker skin pigmentation and melanin, may make the oxygen level estimated value appear higher than it actually is. Users are strongly recommended to establish a baseline value when healthy and at rest. It is recommended that users consult a licensed healthcare provider or professional on how to interpret user readings based on physical traits or characteristics.
CONTEC CMS50N BLack pulse oximeter
Instructions
The CMS50N Pulse Oximeter adopts Photoelectric Oxyhemoglobin Inspection Technology in accordance 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 being used 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).
Features
1) Can measure SpO2 and Pulse Rate accurately
2) SpO2 and Pulse Rate display,Pulse Rate waveform and bar graph display
3) Battery voltage low indication
4)Auto standby
5) The display mode can be changed(Option)
6) Screen brightness adjustable
7) Shut off automatically when no signal
Main performance
●Display Mode：0.96" TFT display.
Screen resolution: 160*80.
●SpO2 measurement range: 0%~100% (resolution: 1 %).
Accuracy: 70%~100%: ±2%.
0%~69%: unspecified.
●PR measurement range: 30bpm~250bpm (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: Under normal and ambient light conditions, the SpO2 deviation ≤ 1%.
●Working current: ≤30mA
●Power supply: two “AAA” batteries
●Safety classification: type BF applied part
Buy safe Products
The following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE:
The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.If the item is subject to FDA regulation,We will verify your status as an authorized purchaser of this item before shipping of the item.If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health.
The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE,TUV of Europe.The Fingertip Pulse Oximeter that is FDA 510K Approved
Only English User manual,Please contact us if you need other language version.This product is sold worldwide, if you are using it in the United States please contact me before purchasing.