FDA Pulse Oximeter Finger Blood Oxygen SpO2 saturation oximetro monitor - JIMFRA
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FDA Pulse Oximeter Finger Blood Oxygen SpO2 saturation oximetro monitor

FDA Pulse Oximeter Finger Blood Oxygen SpO2 saturation oximetro monitor

USD 8.99 USD
SKU: EqFKIKId
Condition: New
Categories: Ventile & Verteiler

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
ModelCMS50M
MPNDoes Not Apply
Country/Region Of ManufactureChina
Included ProbeAdult Finger Probe
Intended Use/DisciplineFamily Medicine

Finger pulse oximeter,spo2 heart rate monitor,blood oxygen 1.Introduction CMS50M 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. CMS50M Pulse Oximeter is applicable for use in plateau area, community healthcare, oxygen bar, Fitness clubs, physical training room, family and medical institution, etc. 2.Features 1) Can measure SpO2 and Pulse Rate accurately 2) SpO2 and Pulse Rate display,bar graph display 3) Battery voltage low indication 4) Shut off automatically when no signal 3.Performance SpO2 measurement range: 0%~100% Accuracy: 70%~100%: ±2% 0%~69%: unspecified PR measurement range: 30bpm~250bpm Accuracy: ±2bpm or ±2%, whichever is greater. Resolution: SpO2: 1% PR: 1bpm Measurement 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: ≤25mA Power supply: two “AAA” batteries Safety classification: type BF applied part 4.Physical characteristic Dimension: 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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