Lens, intraocular, posterior chamber - ARTG 483005
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 483005 and sponsored by IQ Medical, manufactured by Ophtec BV in Netherlands. The device registration started on March 18, 2025.
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.
A device made of acrylic material intended to be implanted permanently in the posterior chamber of the eye, to replace the natural cataractous crystalline human eye lens. This implanted posterior chamber intraocular lens is intended to restore useful vision and is implanted following cataract removal.