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CPAP/BiPAP nasal mask, reusable

Australia TGA ARTG Registered Device · Air Liquide Healthcare Pty Ltd · Air Liquide Medical Systems SRL · Class IIa · Started January 04, 2022

Good Name: Air Liquide Healthcare Pty Ltd - CPAP/BiPAP nasal mask, reusable

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
Start Date
January 04, 2022
Effective Date
January 04, 2022
Sponsor
Manufacturer
Country
Italy
Address
Via Calabria 31, Milano, 20158
Intended purpose

A mask intended for single-patient reuse in the home environment and multipatient reuse in the hospital environment by adult patients for whom a continuous positive airway pressure therapy (CPAP), Bi-Level positive airway pressure therapy (BiPAP), or a respiratory support with positive expiratory pressure therapy (PEP), has been prescribed.

About this record

Access comprehensive regulatory information for CPAP/BiPAP nasal mask, reusable 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 Air Liquide Medical Systems SRL in Italy. The device registration started on January 04, 2022.

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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