Portable CA10M Mainstream ETCO2 Capnograph End tidal CO2 Monitor Respiratory VET
The item CMS50M is made by CONTEC, it is LED screen with SpO2 and Pulse Rate display. Power supply is two “AAA” batteries, there is 1 main unit, 1 user manual, 1 strip and 1 carry case in the package. Battery voltage is low indication, it will Shut off automatically when ther is no signal. CA10M Mainstream ETCO2 Capnograph Respiration Rate End-tidal CO2 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. 1End-tidal CO2 measurement function. 2Respiration rate measurement function. 3Over-limit alarm function for End-tidal CO2 and respiration rate. 4Low battery alarm function. 1Measurement range: 0 150mmHg. 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. Adult gas path adapter. Neonate gas path adapter (optional). Weight: 97g (with batteries). Relative humidity: 30% 75%, no condensation. Power supply: DC 3V (2 AAA dry batteries). Please pay within 2 days so as to avoid unnecessary delays and to ensure you get your item ASAP. An unpaid strike will be sent if the item has not been paid after 14 days. 100% satisfaction is our goal! Client is reaponsible for the custom cleatance and custom duty. If you have a defective item, you want to return or discount. Food and Drug Administration and state and local regulatory agencies. 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. Hope you can understand! All emails will be answered within 24 hours on weekdays(but within 48hours on weekends). Only English user guide, if you need any other languange, please contact me.