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Osteotome - ARTG 463946

Access comprehensive regulatory information for Osteotome in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 463946 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by DePuy Ireland UC in Ireland. The device registration started on October 09, 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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TGA ARTG Official Data
Class I
ARTG 463946
Class I
Osteotome
ARTG ID: 463946
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Osteotome
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Intended Purpose

A reusable surgical instrument with a bevelled cutting edge used during an osteotomy or for shaping bone.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
463946
Start Date
October 09, 2024
Effective Date
October 09, 2024
Manufacturer
Country
Ireland
Address
Loughbeg Ringaskiddy, Co Cork