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Patient positioning device, diagnostic imaging/radiotherapy, moulding, thermoplastic - ARTG 462972

Access comprehensive regulatory information for Patient positioning device, diagnostic imaging/radiotherapy, moulding, thermoplastic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 462972 and sponsored by Whiteley Medical Supplies Pty Ltd, manufactured by Kinetec SAS in France. The device registration started on September 27, 2024.

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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Class I
ARTG 462972
Class I
Patient positioning device, diagnostic imaging/radiotherapy, moulding, thermoplastic
ARTG ID: 462972
Good Name: Whiteley Medical Supplies Pty Ltd - Patient positioning device, diagnostic imaging/radiotherapy, moulding, thermoplastic
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Intended Purpose

A range of thermoplastic materials used to fabricate splints and orthoses . The materials are commonly softened by heating in hot water and while softened are moulded around the patient's body. When cooled the materials harden to form a splint.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
462972
Start Date
September 27, 2024
Effective Date
September 27, 2024
Manufacturer
Country
France
Address
Rue Maurice, Perin ZI de Tournes, Tournes, 08090