Description
Introduction
The device adopts mainstream method to measure the parameters related to EtCO2 and AWRR. It can detect pulmonary ventilation function and reflect the circulation and pulmonary blood flow condition, as well as indirectly reflect the alveolar ventilation, which is applicable for use in emergency department, ICU, operating room, respiratory department and other occasions for adult and pediatric patients. The Capnograph connects with patient’ respiratory tract by the air adapter (applied part) and breathing tube. The breathing tube except for air adapter is not a part of the device.
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: 0 ~150mmHg
2）Resolution: 1mmHg
3）Accuracy:
0～40 mmHg：±2 mmHg
41～70 mmHg：±5% of readings
71～100 mmHg：±8% of readings
101～150 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：< 3s
3）Alarm sound pressure level: 50 dB
4）Battery life time：4hours
Accessories
★ A User Manual
★ An Adult/Pediatric air adapter
Physical Characteristic
Dimension: 59×56×59.5mm
Weight: 92g (with batteries)
Working environment
Temperature: 5℃~40℃
Shipping
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- Clearance: we will ship your item to your confirmed address.
- Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.
Terms of Sale
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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 Co.,Ltd; 20 Years manufacturer,we have stock in USA and China.
Contact Us
Contact Name:Tessy Zhang; Whatsapp/Mobile:+86-18716007715;