Australia TGA ARTG recordNebulizer, non-heated
Australia TGA ARTG Registered Device · Air Liquide Healthcare Pty Ltd · Apex Medical Corp · Class IIa · Started September 16, 2019
Good Name: Air Liquide Healthcare Pty Ltd - Nebulizer, non-heated
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- September 16, 2019
- Effective Date
- September 16, 2019
- Country
- Taiwan
- Address
- No 9 Min Sheng St Tu-cheng, New Taipei City, 23679
To provide a source of compressed air for aerosol therapy. It is used in conjunction with a jet (pneumatic) nebuliser to produce medicated aerosols for inhalation by pediatric and adult patients with respiratory symptoms.
Access comprehensive regulatory information for Nebulizer, non-heated 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 Apex Medical Corp in Taiwan. The device registration started on September 16, 2019.
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.