Introduction
Principle of the CMS50E Pulse Oximeter is as follows: Photoelectric Oxyhemoglobin Inspection Technology is adopted in accordance with Capacity Pulse Scanning & Recording Technology,the Pulse Oximeter can be used in measuring the pulse oxygen saturation and pulse rate through finger.The product is suitable for being used in family, hospital, oxygen bar, community healthcare, physical care in sports (It can be used before or after doing sports, and it is not recommended to use the device during the process of having sport) and etc.
Major Features
Integrated with SpO2 probe and processing display module
Small in volume,light in weight and convenient in carrying
Operation of the product is simple ,low power consumption
Operation menu for the function setting
SpO2 value display
Pulse rate value display, bar graph display
Pulse waveform display
The display mode can be changed
Screen brightness can be changed
A pulse rate sound indication
With measured data overruns limits and low-voltage alarm function,the upper/down alarm range can be adjustable
Battery capacity indication
Low-voltage indication: low-voltage indicator appears before working abnormally which is due to low-voltage,and with alarm function
With SpO2 value and pulse rate value of storage, the storage data can be uploaded to computers)
Real-time data can be transmitted to computers
Automatically power off function: when the device is under the state of measuring interface . it will automatically power off within 5 seconds if the finger falls out of probe.
RF Wireless communication function(option)(only applied for Ver6.6R or above )
Connected with an external oximeter probe(option)(only applied for Ver6.6R or above )
Main performance
Display Mode:1.3" 65K Color OLED display
Screen Resolution:128*96
SpO2 Measuring Range:0%~100%, (the resolution is 1%).
Accuracy:70%~100%:±2% ,Below 70% unspecified.
PR Measuring Range:30bpm~250bpm, (the resolution is 1bpm)
Accuracy:±2bpm or ±2% (select larger)
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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.We only have the English Manual in the standard package, If you need any other language Manual, please contact us freely