Endotherapy guidewire, reusable - ARTG 213456

Access comprehensive regulatory information for Endotherapy guidewire, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 213456 and sponsored by Promis Medical Australia Pty Ltd, manufactured by Pro MIS Medical Sytems GmbH in Germany. The device registration started on August 21, 2013.

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.