Ophteis FR Pro - Aqueous/vitreous humour replacement medium - ARTG 427870

Access comprehensive regulatory information for Ophteis FR Pro - Aqueous/vitreous humour replacement medium in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 427870 and sponsored by Kevin Grundy (IBD) Pty Ltd, manufactured by Rayner Intraocular Lenses Ltd in United Kingdom. The device registration started on November 14, 2023.

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.