CA10M Capnograph
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℃

Payment

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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.

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