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Femoral stem trial prosthesis - ARTG 471765

Access comprehensive regulatory information for Femoral stem trial prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 471765 and sponsored by Amplitude Australia Pty Ltd, manufactured by Amplitude in France. The device registration started on December 04, 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 IIa
ARTG 471765
Class IIa
Femoral stem trial prosthesis
ARTG ID: 471765
Good Name: Amplitude Australia Pty Ltd - Femoral stem trial prosthesis
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Intended Purpose

An invasive medical device representative of a final femoral stem prosthesis, designed to be used in femoral preparation and trial reductions during hip arthroplasty, to assess the correct offset, leg-length, and range of motion of the final femoral prosthesis to be implanted. This is a reusable device intended to be sterilized prior to use.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
471765
Start Date
December 04, 2024
Effective Date
December 04, 2024
Manufacturer
Country
France
Address
11 Cours Jacques Offenbach ZA Mozart 2, Valence, 26000