Introduction
1）Equipment purpose
The device adopts mainstream method to measure the end-tidal carbon dioxide (ETCO2) and airway respiration rate (AwRR).
2） Patient population
The application population is adult, child and infant patients.
3）Applicable place
The device is applicable for use in emergency department, ICU, operating room and respiratory department.
3.1.2 Use requirement
It needs to be used with a ventilator or anaesthetic machine. It connects with patient’s respiratory tract by the airway adapter (applied part) and breathing tube. The breathing tube except for airway adapter is not a part of the device. Ventilator or anaesthetic machine shall meet the CE requirements..
Features
1) End-tidal CO2 measurement function;
2) Respiration rate measurement function;
3) Optional three units;
4) With audible and visual alarm and silencing functions, the alarm limit can be set;
5) Over-limit alarm function for End-tidal CO2 and respiration rate;
6) Low battery alarm function;
7) With the prompt function of “Adapter off”;
8) User can calibrate zero by themselves.
9) With atmospheric pressure and temperature compensation functions;
10) Install 2 AAA dry batteries, up to 4-hour user time.
Performance
★ End-tidal CO2 measurement:
1）Measurement range: 0mmHg~150mmHg
2）Resolution: 1mmHg
3）Accuracy: 0mmHg～40 mmHg: ±2 mmHg
41mmHg～70 mmHg：±5% of readings
71mmHg～100 mmHg：±8% of readings
101mmHg～150 mmHg：±10% of readings
★ Respiration rate measurement:
1）Measurement range: 2rpm～150rpm
2）Resolution: 1rpm
3）Accuracy: ±1rpm
★ Safety characteristic:
1）Device type: internally powered equipment
2）The degree of protection against electric shock: type BF applied part
3）The degree of protection against ingress of liquid: IP22
Other parameters：
1）Preheat time:15s
2）Response time:< 0.5s
3）Alarm sound pressure level: 50 dB
4）Battery life time:4hours
Accessories
★ A User Manual
★ Airway adapter(MGN0011)
Physical Characteristic
Dimension: 59×56×59.5mm
Weight: about 92g (with batteries)
Working environment
Temperature: 5℃~40℃
Relative humidity: 30%~ 75%, no condensation
Atmospheric pressure: 700hPa~1060hPa
Power supply: DC 3V (2 AAA dry batteries)
Input power: ≤1VA
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