Pulse oximeter OLED Finger Heart Rate Oxymetre SpO2 PR Blood Oxygen Monitor FDA

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Pulse oximeter OLED Finger Heart Rate Oxymetre SpO2 PR Blood Oxygen Monitor FDA

Pulse oximeter OLED Finger Heart Rate Oxymetre SpO2 PR Blood Oxygen Monitor FDA

USD 9.99 USD
SKU: AFu84xEb
Condition: New

Specifications

Return Shipping Will Be Paid ByBuyer
All Returns AcceptedReturns Accepted
Item Must Be Returned Within60 Days
Refund Will Be Given AsMoney Back
MPN69450401
Country/Region Of ManufactureChina
Bundle ListingYes
Featured RefinementsFinger Pulse Oximeter
ModelCMS50NA
Form FactorFingertip
BrandCONTEC

Brief introduction 1.Introduction CMS50NA 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.Features 1) 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.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: ≤30mA Power supply: two “AAA” batteries Safety classification: type BF applied part 4.Physical characteristic Dimension: 57mm(L) × 34mm(W) × 31mm(H)Buy Safe Product!!■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.■The model is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923,and certified by FDA 510K Approved of America and CE,TUV of Europe Only English User Manual,Please contact us if you need other language manual.

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