Australia TGA ARTG record

Orthopaedic trocar

Australia TGA ARTG Registered Device · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy Mitek (a Johnson & Johnson Company) · Class IIa · Started July 04, 2016

Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Orthopaedic trocar

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: July 04, 2016
Effective Date: July 04, 2016

Sponsor

Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes

Manufacturer

Name: Depuy Mitek (a Johnson & Johnson Company)
Country: United States of America
Address: 325 Paramount Drive, Raynham, MA, 02767

Intended purpose

A rigid hand-held surgical instrument with a sharp point used to manually puncture a bodily entry point.

About this record

Access comprehensive regulatory information for Orthopaedic trocar in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Depuy Mitek (a Johnson & Johnson Company) in United States of America. The device registration started on July 04, 2016.

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.