Infant Hand-held Pulse Oximeter with USB port Software, for Pediatric, Neonatal
Principle of the CMS60D 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. Light in weight and convenient in carrying. Operation of the product is simple, low power consumption. Operation menu for the function setting. Pulse rate value display, bar graph display. Screen brightness can be changed. With measured data overruns limits and low-voltage alarm function. 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. Connected with an external oximeter probe. Display Mode : 1.8 Color OLED display. 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). Measurement Performance in Weak Filling Condition:SpO2 and. Pulse rate can be shown correctly when pulse-filling ratio is 0.4%.Pulse rate error is ±2 bpm or ±2% (select larger). 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%.
Power Consumption : less than 100mA. Voltage: DC 2.6V3.6V. Power Supply: Dry battery(2AA). Battery working hour: Theoretical number is 44 hours. Safety Type:Interior Battery , BF Type. Food and Drug Administration and state and local regulatory agencies. 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.100% satisfaction is our goal! We are looking forward to establishing a successful business relationship with you. Only english user guide, if you need any other language, please contact me.