ARTG 461605Bone-resection orthopaedic reamer, single-use
ARTG ID: 461605 · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · DePuy Ireland UC · Class IIa · Started August 30, 2024
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Bone-resection orthopaedic reamer, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 461605
- Start Date
- August 30, 2024
- Effective Date
- August 30, 2024
- Name
- DePuy Ireland UC
- Country
- Ireland
- Address
- Loughbeg Ringaskiddy, Co Cork
A surgical instrument designed to resect and shape an area of bone for the acceptance of an implant. This is a single-use device.
Access comprehensive regulatory information for Bone-resection orthopaedic reamer, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 461605 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by DePuy Ireland UC in Ireland. The device registration started on August 30, 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.