Australia TGA ARTG recordBath, water, thermoplastic moulding/splint
Australia TGA ARTG Registered Device · Rehacare Pty Ltd · Kinetec SAS · Class I · Started March 10, 2020
Good Name: Rehacare Pty Ltd - Bath, water, thermoplastic moulding/splint
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 10, 2020
- Effective Date
- March 10, 2020
- Name
- Rehacare Pty Ltd
- Name
- Kinetec SAS
- Country
- France
- Address
- Rue Maurice, Perin ZI de Tournes, Tournes, 08090
A water bath designed for the warming/heating of mouldable plastic materials used to create body positioning, and body fixation devices. This device consist of a large water holder (pan) that is temperature-regulated
Access comprehensive regulatory information for Bath, water, thermoplastic moulding/splint in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Rehacare Pty Ltd, manufactured by Kinetec SAS in France. The device registration started on March 10, 2020.
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.