Australia TGA ARTG recordCold air therapy unit
Australia TGA ARTG Registered Device · Aussie Medi Tech Pty Ltd · Zimmer MedizinSysteme GmbH · Class IIa · Started August 05, 2023
Good Name: Aussie Medi Tech Pty Ltd - Cold air therapy unit
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- August 05, 2023
- Effective Date
- August 05, 2023
- Country
- Germany
- Address
- Junkersstrasse 9, Neu-Ulm, 89231
A device intended to generate and deliver a stream of cold air directly to the skin surface to treat musculoskeletal/rheumatic disorders, to reduce localised pain/inflammation, and/or reduce thermal skin damage during dermatological laser treatments.
Access comprehensive regulatory information for Cold air therapy unit in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Aussie Medi Tech Pty Ltd, manufactured by Zimmer MedizinSysteme GmbH in Germany. The device registration started on August 05, 2023.
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.