Lens, intraocular, posterior chamber - ARTG 473806
Access comprehensive regulatory information for Lens, intraocular, posterior chamber in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 473806 and sponsored by AMO Australia Pty Ltd, manufactured by Johnson & Johnson Surgical Vision Inc in United States of America. The device registration started on December 18, 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.
The device is intended to correct aphakia following removal of the natural crystalline lens.

