Reference. 1237CO2CAN-I
O2/CO2 Nasal Cannula for Capnography with Luer-Lock Connector. Pediatric
O2/CO2 cannula for babies, intended for continuous monitoring of exhaled CO2 in non-intubated patients while receiving supplemental oxygen, with Luer-Lock connection.
Description
The cannula is designed to continuously monitor exhaled carbon dioxide (CO2) in non-intubated infants using a gas analyzer, while also allowing the administration of supplemental oxygen.
The CO2 cannulas connect the patient to the gas analyzer. During use, exhaled gases are taken through a tube that connects the cannula to the analyzer, where continuous CO2 measurement is performed.
It is made of a soft material that allows it to be comfortably placed over the baby's ears.
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 hydrophobic filter.
- Without hydrophobic membrane.
- Cannula made of PVC.
- Infant version for babies.
- Packaging: individual polyethylene (PE) bag.
- Non-sterile product.
- Medical device class: IIa, non-sterile.
- In accordance with Directive 93/42/EEC on medical devices.
*Intended for use by healthcare professionals. Use in accordance with the manufacturer's instructions and the protocols established by the healthcare center.
The CO2 cannulas connect the patient to the gas analyzer. During use, exhaled gases are taken through a tube that connects the cannula to the analyzer, where continuous CO2 measurement is performed.
It is made of a soft material that allows it to be comfortably placed over the baby's ears.
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 hydrophobic filter.
- Without hydrophobic membrane.
- Cannula made of PVC.
- Infant version for babies.
- Packaging: individual polyethylene (PE) bag.
- Non-sterile product.
- Medical device class: IIa, non-sterile.
- In accordance with Directive 93/42/EEC on medical devices.
*Intended for use by healthcare professionals. Use in accordance with the manufacturer's instructions and the protocols established by the healthcare center.







