Description: Description The pulse oximeter,based on all digital technology, is intended for noninvasive spot -check measurement of functional oxygen stautation of arterial hemoglobi (SpO2).Advanced DSP algorithm can reduce the influence of motion artifact and improve measurement accuracy of low perfusion. Features Real spot-checks Pulse waveform & bargraph display Advanced setting for alarm Functions of audio alarm and pulse sound Automatic power off Low power consumption down to 0.3% 50 hours continuous to work Low perfusion ≤0.4% Low voltage indicator Widely used in hospital, home healthcare, oxygen bar, community medical centre, alpine area, sports healthcare etc. Specification Display OLED two color display SpO2 Measurement range: 70～99% Resolution: ±1% Accuracy: ±2% (70%～99%), unspecified (<70%) Pulse rate Measurement range: 30～240 bpm Resolution: ±1% Accuracy: ±2bpm or ±2% (select larger) Low Perfusion ≤0.4% Power 1.5V (AAA size) alkaline battery x 2 Supply voltage: 2.6~3.6V Working current ≤30mA Automatic power-off Automatically power off when no signal in the oximeter for more than 8 seconds Dimension & Weight 58 (L) × 31(W) × 29(H) mm 60g Packing List Fingertip Oximeter x1 Lanyard x1 English user's manual x1 FDA Disclaimer: Statement：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 so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item. This item has been cleaned and treated according to the manufacturer's instructions.Abigail-China-Beijing-86-18142769213 The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136606. The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number：K132989 The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number：K180353 The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number：K141973 massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number：K161892 Ultrasound ,Ultrasonic Treatment Device is certified with the US FDA 510(k) Number：K161892 This item has been cleaned and treated according to the manufacturer's instructions.
Price: 6.78 USD
Location: Cranbury, New Jersey
End Time: 2024-10-19T04:32:37.000Z
Shipping Cost: 0 USD
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Item Specifics
Restocking Fee: No
Return shipping will be paid by: Buyer
All returns accepted: Returns Accepted
Item must be returned within: 30 Days
Refund will be given as: Money Back
Brand: Carejoy
MPN: Does Not Apply
