Australia TGA ARTG record

Wound hydrogel dressing, sterile

Australia TGA ARTG Registered Device · Johnson & Johnson Pacific Pty Ltd · Johnson & Johnson GmbH · Class IIa · Started January 24, 2018

Good Name: Johnson & Johnson Pacific Pty Ltd - Wound hydrogel dressing, sterile

Device classification

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

Registration information

Start Date: January 24, 2018
Effective Date: January 24, 2018

Sponsor

Name: Johnson & Johnson Pacific Pty Ltd

Manufacturer

Name: Johnson & Johnson GmbH
Country: Germany
Address: Johnson & Johnson Platz 2, Neuss, 41470

Intended purpose

Sterile and non-sterile self-adhesive hydrocolloid dressings for short-term use to protect and manage the micro-environment of superficial wounds and promote healing.

About this record

Access comprehensive regulatory information for Wound hydrogel dressing, sterile in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Johnson & Johnson Pacific Pty Ltd, manufactured by Johnson & Johnson GmbH in Germany. The device registration started on January 24, 2018.

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.