Black CMS50N OLED Fingertip Pulse Oximeter, Spo2 Monitor,Carry Case,Lanyard

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Black CMS50N OLED Fingertip Pulse Oximeter, Spo2 Monitor,Carry Case,Lanyard

Black CMS50N OLED Fingertip Pulse Oximeter, Spo2 Monitor,Carry Case,Lanyard

USD 9.99 USD
SKU: GTodYMHN
Condition: New

Specifications

Return Shipping Will Be Paid BySeller
All Returns AcceptedReturns Accepted
Item Must Be Returned Within60 Days
Refund Will Be Given AsMoney Back
BrandCONTEC
Form FactorFingertip
ModelCMS50NA
MPNDoes not apply
Country/Region Of ManufactureChina
Included ProbeAdult Finger Probe
Intended Use/DisciplineFamily Medicine

CMS50NA Pulse Oximeter 1.IntroductionCMS50NA Pulse Oximeter is a portable equipment adopting advanced technology, it mainly checks SpO2 and PR value through the finger, which provides advanced, non-invasive and scientific means for quantitative measurement of oxygen saturation. CMS50NA Pulse Oximeter is applicable for use in plateau area, community healthcare, oxygen bar, Fitness clubs, physical training room, family and medical institution, etc. 2.Features1) Can measure SpO2 and Pulse Rate accurately2) SpO2 and Pulse Rate display,Pulse Rate waveform and bar graph display 3) Battery voltage low indication4) The display mode can be changed.5) Screen brightness adjustable3.PerformanceSpO2 measurement range: 0%~100%Accuracy: 70%~100%: ±2% 0%~69%: unspecifiedPR measurement range: 30bpm~250bpmAccuracy: ±2bpm or ±2%, whichever is greater.Resolution: SpO2: 1% PR: 1bpmMeasurement Performance in Weak Filling Condition: SpO2 and pulse rate can be shown correctly when pulse-filling ratio is 0.4%. SpO2 error is ±4%, pulse rate error is ±2 bpm or ±2%, whichever is greater.Resistance to surrounding light: The deviation between the value measured in the condition of man-made light or indoor natural light and that of darkroom is less than ±1%.Working current: ≤30mAPower supply: two “AAA” batteriesSafety classification: type BF applied part 4.Physical characteristicDimension: 57mm(L) × 34mm(W) × 31mm(H) 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.

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