LED Fingertip Finger Pulse Oximeter SpO2 PR PI Blood Oxygen Meter Monitor CE&FDA

Description

CE&FDA
Features:
Color OLED display, simultaneous display for testing value and plethysmogram
The display interface of OLED can rotate four directions whith six different display modes after pressing the power button for less than 0.5s.
PI Indicator: Perfusion Index.It reflects the amount of blood flow being measured by the oximeter. A health care professional tests blood flow to establish norms and aid in identifying changes in a patient's condition.
Advanced DSP algorithm inside minish the influence of motion artifact and improve accuracy of low perfusion.
Low voltage indicator
The oximeter will automatic power off after 8 seconds when no signal.
Low-power consumption, continuously work for 50 hours.
Small in volum,light in weight,convenient to carry,convenient to use and to storage.
Widely used in hospital,home healthcare,oxygen bar,community medical centre,alpine area, sports healthcare etc.
Specification:
Hemoglobin saturation display: 35-100%
Pulse rate Display: 25-250 BPM
Power Consumption: Smaller than 30mA(Normal)
Resolution:
Hemoglobin Saturation (SpO2): 1%
Pulse rate: 1BPM
Measurement Accuracy:
Hemoglobin Saturation(SpO2 ): (80%-100%): 2% unspecified(≤70%)
Pulse rate: 2BPM
Measurement Performance in Low perfusion Condition: 0.2%
Perfusion Index:1%
Battery: 2 AAA 1.5V alkaline batteries(Not Include)
Weight: 50g/1.76oz
Package Content:
1x Fingertip Pulse Oximeter
1x Lanyard
1x English user's manual
FDA declaration :
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.(CICI-China-86-18328503374)
This item has been cleaned and treated according to the manufacturer's instructions.
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.
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