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CMS50QB Child Pulse Oximeter KIDS Infant Baby Blood Oxygen Monitor SPO2 Probe PR - 第 12/21 張圖片
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Introduction

The CMS50QA Pulse Oximeter adopts Photoelectric Oxyhemoglobin Inspection Technology in accordance with Capacity Pulse Scanning & Recording Technology, which can be used to measure human oxygen saturation and pulse rate through finger. The device is suitable for being used in family, hospital, oxygen bar, community healthcare and physical care in sports, etc. (It can be used before or after exercise, but not recommended to use during exercising).

Features
A.SpO2 value display.
B.PR value and bar graph display.
C.Low-battery indication: low-battery indication appears when the battery voltage is too low to work.
D.Automatic standby function.
E.Charging function.
F.PR sound indication; sound prompt for over-limit, low battery.

Performance
●Display mode: TN Segment LCD
●SpO2 measurement range: 0%~100% (resolution: 1 %)
Accuracy: 70%~100%: ±2%
 0%~69%: unspecified
●PR measurement range: 30bpm~250bpm (resolution: 1 bpm)
Accuracy: ±2 bpm or ±2%, whichever is greater.
●Accuracy under low perfusion: low perfusion 0.4 %, SpO2 accuracy: ± 4 %; PR accuracy: ± 2 bpm or ± 2 %, whichever is greater.
●Light interference: compared to the values measured in normal condition and ambient light condition, the deviation: ≤ ± 1 %.
●Power consumption: ≤ 70 mA
●Working voltage:DC 3.6 V - 4.2 V
●Battery: A rechargeable lithium battery (3.7V)
●Battery life: Charge and discharge: no less than 500 times.
●Safety class: Internally powered equipment, type BF applied part.

Accessories
●one User Manual 
●one lanyard (optional)
●one USB cable (optional)
●one power adapter (optional)

Physical characteristic
Dimension: 46(L) × 40(W) × 29(H) mm
Weight: About 35 g (including a lithium battery)



one User Manual
one lanyard
one USB cable (optional)
one power adapter (optional)

Physical characteristic
Dimension: 46(L) × 40(W) × 29(H) mm
Weight: About 35 g (including a lithium battery)


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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 Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG)with the code 197923, and certified by FDA of United States and CE,TUV of Europe. The  Fingertip Pulse Oximeter that is FDA 510K Approved

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Import duties,Taxes are not included in the item price.These charges are buyers' responsibility


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