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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 Air Liquide Healthcare Pty Ltd, manufactured by INOSYSTEMS SA in France. The device registration started on June 04, 2024.

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: Air Liquide Healthcare Pty Ltd - Tube/mask breathing circuit connector, non-sterile, single-use
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Intended Purpose

Intended for the delivery of gases during inhaled Nitric Oxide therapy with the Nitric Oxide delivery and monitoring system. It is located between the adapter from the main device and the flow sensor adapter.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
June 04, 2024
Effective Date
June 04, 2024
Manufacturer
Country
France
Address
7 rue Georges Besse, Antony, 92160