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O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor

O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor
O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor

O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor

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. 3Over-limit alarm function for End-tidal CO2 and respiration rate.

41~70 mmHg:±5% of readings. 71~100 mmHg:±8% of readings.

101~150 mmHg:±10% of readings. 1Device type: internally powered equipment. 2Degree of protection against electric shock: type BF applied part.

3Degree of protection against ingress of liquid: IPX2. Neonate gas path adapter (optional). Relative humidity: 30% 75%, no condensation. Power supply: DC 3V (2 AAA dry batteries). Food and Drug Administration and state and local regulatory agencies. 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. Please use under the doctor's instruction. You pay us what you see on the invoice, i.

Or replace item for you free of charge. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Patient Monitors". The seller is "happystore2017" and is located in this country: CN. This item can be shipped to United States, all countries in Europe, all countries in continental Asia, Canada, Australia.

  • Model: CA10M
  • Country/Region of Manufacture: China
  • Technology: Digital
  • MPN: 69450401
  • Monitor Parameters: CO2 - EtCO2
  • Brand: CONTEC

O2 Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 patient Monitor