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Tube/mask breathing circuit connector, non-sterile, single-use

Access comprehensive regulatory information for Tube/mask breathing circuit connector, non-sterile, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Airlife Australia Holdings Pty Ltd, manufactured by Vyaire Medical Oy in Finland. The device registration started on November 27, 2020.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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TGA ARTG Official Data
Class IIa
Class IIa
Tube/mask breathing circuit connector, non-sterile, single-use
Australia TGA ARTG Registered Device
Good Name: Airlife Australia Holdings Pty Ltd - Tube/mask breathing circuit connector, non-sterile, single-use
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Pricing
Intended Purpose

Use the adapter for measuring CO2, O2, N2O and anesthetic agents. Products are in indirect patient contact via gas passing through sampling site. This product is to be used only by professional healthcare personnel.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
November 27, 2020
Effective Date
November 27, 2020
Manufacturer
Country
Finland
Address
Kuortaneenkatu 2, Helsinki, FI-00510