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Bath, water, thermoplastic moulding/splint

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.

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TGA ARTG Official Data
Class I
Class I
Bath, water, thermoplastic moulding/splint
Australia TGA ARTG Registered Device
Good Name: Rehacare Pty Ltd - Bath, water, thermoplastic moulding/splint
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Intended Purpose

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

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
March 10, 2020
Effective Date
March 10, 2020
Sponsor
Manufacturer
Country
France
Address
Rue Maurice, Perin ZI de Tournes, Tournes, 08090