Introduction
The CMS60F 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
Small in volume, light in weight and convenient in carrying
Easy to operate, low power consumption
Operation menu for function settings
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/lower alarm limit can be adjusted
Battery capacity indication
Low-voltage indication: low-voltage indication appears before working abnormally which is due to low-voltage, and with alarm function
With clock function
Review function
With data record function of multi-user
Touch key operation and locking touch key function
It can be connected with external SpO2 probe
Performance
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% (whichever is greater)
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% (whichever is greater).
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: 3.7V rechargeable lithium battery × 1
Battery working hour: 10 hours in theoretical
Battery service life: no less than 500 times of charge and discharge
Safety type: Internally powered equipment, Type BF applied part
Accessories
◆A User Manual
◆A power adapter
◆a data line
◆A SpO2 probe
Physical characteristic
Dimension: 98(L) × 58(W) × 12(H) mm
Weight: about 65g (with a lithium battery)
Shipping
* Clearance: we will ship your item(s) to your PayPal
confirmed address.Please leave me your clear address,telephone,postal code.
* It is the buyers' responsibility to consider duties,
taxes and other extra charges by the government in your respective country.
* All items will be dispatched within 1 business day.
* The item will be declared as lower value for shipping
only.We'd like to cooperate with you and declare the value of it as you want us
to, so that it is more easier for you to clear the custom.
Terms of Sale
There are not extra taxes, VAT or other unmentioned
payment. You pay us with goods subtotal + shipping cost (not include duties).
But you need to pay for the import duties in case that occurred for certain
goods, or you may kindly give us some suggestions about that,we promise to do
our best to help you!
Feedback
Feedback:please leave me a positive feedback if you are
satisfied with our products, Your positive feedback will be appreciated very
much!If you have any problems, please contact us to solve it before openning a
case or leave negative feedback,Thank you.
Return - After service
We offer 60 days return policy. 100% satisfaction is our
goal!
1.All items are brand new ,with 1 years warranty.
2.If you have a defective item, you want to return or
discount. Please contact us within 2 days from you receive the shipment.
3.We will refund the money to you when we get the return
items or replace item for you.
4. All return items must be returned with it's original
packaging and accessories. Customer is responsible for shipping charges on
returned items.
Buy safe Products
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.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.
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
About Us
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.