CO2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 Monitor,CA10M NEW

               
Introduction
Capnograph adopts mainstream method to measure the end-tidal carbon dioxide, airway respiration rate and other parameters. 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 pre-hospital emergency transfer, emergency department, ICU, operating room, neonatology, respiratory department and other occasions. The application population is adult, pediatric and neonate patients. The Capnograph connects with patient’ respiratory tract by the airway adapter and breathing tube.

Features
1)End-tidal CO2 measurement function
2)Respiration rate measurement function
3)Over-limit alarm function for End-tidal CO2 and respiration rate
4)Low battery alarm function

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~150rbpm
2)Resolution: 1rpm
3)Accuracy: ±1rpm
Safety characteristic:
1)Device type: internally powered equipment
2)Degree of protection against electric shock: type BF applied part
3)Degree of protection against ingress of liquid: IPX2

Accessories
User Manual
Adult gas path adapter
Neonate gas path adapter (optional)

Physical Characteristic
Dimension: 55×52×59mm
Weight: 97g (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.

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


We are the manufacturer of medical equipment for 17 years, the following are our main products:

ECG /  ECG holter   EEG / EEG Holter      B-ultrasound

Patient Monitor      Fetal doppler             Fetal Monitor 

Spo2 Monitor          Stethoscope              Medical Image....

Agent in the world!

We are look for partners in the world now!

Do you want  to become our agent in you conutry?

Join US!

Sky-pe:xuebox3

contec.med.mary # hotmail dot com

               
           
       
       
   

Only English User Manual,Please contact us if you need other language version.thank youibay365