Description: CONTEC Sidestream ETCO2 Module end tidal CO2 Capnograph for CONTEC monitor NOT include the patient monitor Introduction Introduction CO2-M01 is used to match Patient Monitor. The module adopts sidestream method to measure the parameters related to ETCO2 and AWRR. It can detect pulmonary ventilation function and reflect the circulation and pulmonary blood flow and indirectly reflect the alveolar ventilation. The application population is adult patients. It is applicable for use in emergency department, ICU, operating room, respiratory department and other occasions. It is connected to the nose end of the patient through the sampling tube (applied part). Features 1)End-tidal CO2 measurement function. 2)Inspired Minimum CO2 measurement function. 3)Respiration rate measurement function. 4)Optional three units: %, kPa, mmH. 5)Be compatible with Respironics module’s parameters and protocol. 6)No uesr calibration is required. 7)User can calibrate zero by themselves. 8)With atmospheric pressure and temperature compensation functions. Performance End-tidal CO2 measurement: 1)Measurement range: 0mmHg ~150mmHg; 2) Resolution: 1 mmHg; 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~120rpm; 2)Resolution: 1rpm; 3)Accuracy: ±1rpm; Inspired Minimum CO2 measurement: Measurement range: 3mmHg ~50mmHg; Other parameters: 1)Preheat time: 2min; 2)Response time: < 3s; 3)Sampling frequency: 200 Hz. Safety characteristic 1)Degree of protection against electric shock: type BF applied part; 2)Degree of protection against ingress of liquid: IP22. Accessory 1)A uers manual; 2)A CO2 sampling tube(nasal cannula with filter cotton). Physical Characteristic Dimension: 98.9*54.3*27.6 mm Weight: 165 g Working environment Temperature: 5℃~40℃ Relative humidity: 30%~ 75%, no condensation Atmospheric pressure: 700hPa~1060hPa Power supply: DC 5.0V Input power: ≤0.9VA 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 Return Policy: If you receive a defective item which you want to return, please contact us within 5 days from the day you receive the item. All return items must be returned with its original packaging and accessories. If we confirm the damage happened during the shipment, we will bear the shipping cost for return. We will refund the money to you when we get the return items. Or replace item for you free of charge. 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! Skype:xuebox3 contec.med.mary at hotmail.com
Price: 274.99 USD
Location: Elk Grove Village, Illinois
End Time: 2024-11-12T08:21:23.000Z
Shipping Cost: 0 USD
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Item Specifics
Restocking Fee: No
Return shipping will be paid by: Seller
All returns accepted: Returns Accepted
Item must be returned within: 60 Days
Refund will be given as: Money Back
Brand: CON-TEC
MPN: Does Not Apply
Monitor Parameters: CO2 - EtCO2
Model: Etco2
Country/Region of Manufacture: China
Etco2: Only compatible with CONTEC Brand patient monitor new port
monitor: not include