CMS50E Pulse Oximeter
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.Tips:
USA Buyer: ship from USA warehouse . Fast delivery (2-5 days) ;
OTHER BUYER : SHIP FROM CHINA WAREHOUSE. 1-6 WEEKS DELIVERY
Pulse Oximeter-CMS50EA
Brand : CONTEC Model :CMS50E
Instructions
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)（CMS50EW，only applied for Ver6.6R or above of CMS50E
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)
◆ Measurement Performance in Weak Filling Condition:SpO2 and pulse rate can be shown correctly when pulse-filling ratio is 0.4%. SpO2 error is ±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 3.6V～4.2V
◆ Power Supply:Voltage 3.7 rechargeable lithium battery × 1
◆ Battery working hour:20 hours
◆ Battery working life:Charge and discharge no less than 500 times.
◆Safety Type:Interior Battery，BF Type
Accessories
Sell in standard
◆ a hanging rope
◆ a user manual
◆ a data line
◆ a power adapter （GTM41076-0605;CMS0105）
Sell in addition
Oximeter Probe(Refer to probe application instruction for details and notice renewal）
RF Wireless Module”（only applied for Ver6.6R or above of CMS50E)
Physical Identity
Dimension:57(L) × 32(W) × 30 (H) mm
Weight:About 50g (with the lithium battery*1)
The monitor is registered on the Australian Register of Therapeutic Goods(ARTG) with the code 197923
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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 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