RS01 Sleep apnea screen meter
Description
Introduction
The RS01 device is suitable for the one who suffers with such diseases as SAHS (sleep apnea-hypopnea syndrome), Its functions including patient’s sleep apnea monitoring and SpO2 monitoring, which can be applied in hospital or at home.
Features
1)SpO2 and PR value display, pulse sound and bar graph indication.
2)Pulse waveform and nose flow waveform display
3)Alarms for low power, finger out and exceeding limits
4)Battery status indication
5)Real-time clock
6)Timing power on/off
7)Storage of multiple cases
8)Continuous 12 hours data record
9)Uploading data via USB port
10)PC analysis software
Performance
Nose air flow measurement range: 0 rpm~40 rpm, accuracy: ±2 rpm.
SpO2 measurement range: 0%~100% (resolution 1%), accuracy: 70%~100%, ±2; less than 70%, unspecified.
PR measurement range: 30 bpm~250 bpm, accuracy: ±2 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%.
Power consumption: ≤100 mA.
Power supply: 3.7 V rechargeable lithium battery.
Safety type: internally powered equipment, type BF applied part.
Accessories
A power adapter
A USB data line
A Nasal cannula
Two kinds of SpO2 probes
A CD (PC software)
A User Manual
Physical characteristic
Dimension: 69 mm (L)×50mm (W) ×17.3 mm (H)
Weight: about 100g
Working environment:
Temperature: 10 ℃ ~ 40 ℃
Relative humidity: ≤75 %
Atmospheric pressure: 700 hPa～1060 hPa
Storage environment:
Temperature: -40 ℃ ~ +55 ℃
Relative humidity: ≤95 %
Atmospheric pressure: 500 hPa～1060 hPa
Payment
We accept Paypal Payment.
Shipping
Clearance: we will ship your item to your Ebay confirmed address.
Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.
Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.
Terms of Sale
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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.
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.
Contact Us
Please contact us through Ebay message, we will reply you on line at 24 hours.
Whatsapp/Wechat:+86 18716007715;