CE FDA hand-held Pulse Oximeter with SPO2 monitor, big touch screen, CMS60F
The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923,
The Fingertip Pulse Oximeter that is FDA 510K Approved and certified by FDA of United States and CE,TUV of Europe.
Principle of the CMS60F 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.
◆ 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
◆ PI Display
◆ 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 clock function
◆ Review function
◆ With data record function of multiuser, continuous record about 24 hours data for each user, and the record data can be uploaded to computer
◆ Touch key operation and locking touch key function
◆ It can be connected with adult,child,infant oximeter probe
◆ Wireless communication function（CMS60FW）
◆ Display Mode：2.8" TFT Color display
◆ Screen Resolution：320*240
◆ 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%.
◆ Voltage:DC 3.6V～4.2V
◆ Power Supply:Voltage 3.7 rechargeable lithium battery × 1
◆ Battery working hour: 8 hours
◆ Battery working life:Charge and discharge no less than 500 times.
◆ Safety Type:Interior Battery，BF Type
Sell in standard
◆ a user manual
◆ A power adapter（GTM41076-0605;CMS0105）
◆ a data line
◆ a disk (PC software)
◆ An oximeter probe
Sell in addition
Other Oximeter Probe (Refer to probe application instruction for details and notice renewal）
Dimension:94.25(L) × 55.32(W) × 9.6(H) mm
Weight:About 80g (with a lithium battery)
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1.All items are brand new ,with 1years warranty.
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Contact Person ：Tracy
Contec Medical Systems Co.,Ltd, Manufacturer, Qinhuangdao, China
Address: No.112 Qinhuang West Avenue, Qinhuangdao Economic and Technical Development Zone, Hebei Province, China
Contec Medical Systems focusing on research, manufacture and distribution of medical instruments,was founded in 1992 as a
high-tech company.At present there are more than 1200 employees in our company.Our product line covers a wide range of 13 categories.
Most of the domestic hospitals are our customers.
Contec hopes to cooperate with international companies to supply more innovative design and advanced technology products
We sincerely welcome you to become one of our global partners.We are looking forward to establishing a successful business relationship with you.
FDA K Number
CMS50C Pulse Oximeter
Premarket Submission Number(510K): K073454
Listing Number: D045684
●CMS50D/L/DL Pulse Oximeter
Premarket Submission Number(510K): K082641
Listing Number: D064765
●Sonline A/B,Baby Sound A/BPocket Fetal Doppler
Premarket Submission Number(510K): K082480
Listing Number: D072247
●CMS50E，CMS50F，CMS60C，CMS60D ， Pulse Oximeter
Premarket Submission Number(510K): K090671
Listing Number:D078664，ECG80A ECG machine
Premarket Submission Number(510K): K090936
Listing Number: D081157
If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health:
Phone number: 800.638.2041