Endotherapy guidewire, single-use - ARTG 460065

Access comprehensive regulatory information for Endotherapy guidewire, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 460065 and sponsored by Fresenius Kabi Australia Pty Ltd, manufactured by Fresenius Kabi AG in Germany. The device registration started on August 19, 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.