CONTEC CMS50N Adult Fingertip Pulse Oximeter Spo2 Monitor,Oxygen saturation USA
Specifications
| Return Shipping Will Be Paid By | Buyer |
| All Returns Accepted | Returns Accepted |
| Item Must Be Returned Within | 60 Days |
| Refund Will Be Given As | Money Back |
| Model | CMS50NA |
| Country/Region Of Manufacture | United States |
| Feature | SPO2,PR |
| MPN | 69450401 |
| Brand | CON-TEC |
| Included Probe | Adult Finger Probe |
| Form Factor | Fingertip |
CONTEC CMS50N Adult Fingertip Pulse Oximeter Spo2 Monitor,Oxygen saturation USA Brief introduction Brief introduction 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 adjustable 3.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) 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 On May-10-17 at 00:04:20 PDT, seller added the following information: Only English user guide,if you need any other language,please contact us!
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