Reference. 1237CO2CAN-P
O2/CO2 Nasal Cannula for Capnography with Luer-Lock Connector. Pediatric
Pediatric nasal cannula for continuous monitoring of exhaled CO2 in non-intubated patients receiving supplemental oxygen, with Luer-Lock connection.
Description
The O2/CO2 pediatric cannula is designed to continuously monitor exhaled carbon dioxide in non-intubated pediatric patients using a gas analyzer, while also allowing the administration of supplemental oxygen.
The cannula connects the patient to the gas analyzer. During use, exhaled gases are drawn through a tube from the cannula to the analyzer, where continuous CO2 measurement is performed. Its manufacture in soft material allows it to be comfortably placed over the ears and adapted for pediatric use.
Technical specifications:
- Female Luer-Lock connector.
- Male Luer-Lock connector for tube with an outer diameter of 3 mm.
- Burst pressure: 2 bar (29 psi).
- Without filter or hydrophobic membrane.
- Cannula made of PVC.
- Product intended for pediatric use.
- Packaging: individual polyethylene (PE) bag
- Non-sterile product.
- Medical device class: IIa, non-sterile.
- In compliance with Directive 93/42/EEC on medical devices.
*Intended for use by healthcare professionals. Use in accordance with the manufacturer's instructions and the products established by the healthcare center.
The cannula connects the patient to the gas analyzer. During use, exhaled gases are drawn through a tube from the cannula to the analyzer, where continuous CO2 measurement is performed. Its manufacture in soft material allows it to be comfortably placed over the ears and adapted for pediatric use.
Technical specifications:
- Female Luer-Lock connector.
- Male Luer-Lock connector for tube with an outer diameter of 3 mm.
- Burst pressure: 2 bar (29 psi).
- Without filter or hydrophobic membrane.
- Cannula made of PVC.
- Product intended for pediatric use.
- Packaging: individual polyethylene (PE) bag
- Non-sterile product.
- Medical device class: IIa, non-sterile.
- In compliance with Directive 93/42/EEC on medical devices.
*Intended for use by healthcare professionals. Use in accordance with the manufacturer's instructions and the products established by the healthcare center.







