Australia TGA ARTG recordNebulizer, non-heated
Australia TGA ARTG Registered Device · Ebos Group Australia Pty Ltd · Haemologic Biotech Pty Ltd · Class IIa · Started December 15, 2010
Good Name: Ebos Group Australia Pty Ltd - Nebulizer, non-heated
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- December 15, 2010
- Effective Date
- December 15, 2010
- Country
- Australia
- Address
- D2/15 Narabang Way, BELROSE, NSW, 2085
A device that provides aerosolized humidification or medication for a patient to inspire. The device may include an oxygen or air source to provide generation of the aerosol, a reservoir for the medication, a baffle, and a compressor. The device is for respiratory therapy for home and hospital use.
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 Ebos Group Australia Pty Ltd, manufactured by Haemologic Biotech Pty Ltd in Australia. The device registration started on December 15, 2010.
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.