Sleep apnea screen meter RS01, SPO2 Pulse Rate Air Flow Monitor, Alarm+Software
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
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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 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
International Buyer--Please note:
Import duties,Taxes are not included in the item price.These charges are buyers' responsibility
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