Features
- With 4 parameters : SPO2, PR, PI, ODI4 (Oxygen desaturation Index of 4%) ;
- Support Real-time spot-checks & maximum 8 hours continuous measurement .
Continuous measurement can provide data storing and data analysis function , can be used to make sleep quality monitoring ;
- With alarm & beep function ;
- With 5 levels brightness adjustable ;
- Two color OLED display, 6 display modes & 4 directions display ;
- Automatically standby or sleep after 8 seconds without finger in it ;
- Low-power consumption,continuously four direction adjustable;
- Lightweith for carrying and easy to use .
What's ODI4 ?
- “ODI4” (Oxygen desaturation Index of 4%) means Events of Desaturation which is not less than 4% per hour during the total recording time.
- ODI4 indicates the severity of hypoxia during sleep, if this number is greater than 5, please go to the hospital for further examination.
- The analysis result of ODI may inaccurate when total sleep time is less than 2 hours . The maximum of recording time is 8 hours .
Specifications:
- SpO2
Measurement range: 35~100%
Resolution: ±1%
Accuracy: ±2% (80%~100%) , ±3% (70%~80%) , unspecified (=<70%)
- Pulse rate
Measurement range: 25~250 bpm
Resolution: ±1bpm
Accuracy: ±2bpm
- Perfusion Index ( PI)
Measurement range: 0~30%
Resolution: ±0.1%
Accuracy: ±1% (0%~20%), unspecified (>20%)
- Oxygen Desaturation Index ( ODI4)
- Data Record Hour: up to 8 hours
- Power:1.5V (AAA size) alkaline battery x 2
- Working current: ≤30mA
- Automatic power-of: Automatically power off when no signal in the oximeter after 8 seconds
- Environmental Sepecification
Operating Temperature:5-40 degrees ;
Storage/Transportation Temperature:-20 to 55 degrees Celcius;
Relative Humidity:15-80% on operation;
Order safe product
- 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 so, do not bid on this item unless you are an authorized purchaser. 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 any questions, refer to the FDA website: http://www.fda.gov
- This Item is registered on theAustralian Register of Therapeutic Goods (ARTG) with the code 136606,and certified by FDA of United States and CE, TUV of Europe.Premarket Submission Number(510K): K082641 Listing Number: D064765
- The Item is certified with the US FDA 510K No. K070372, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136605.