ARTG 213456Endotherapy guidewire, reusable
ARTG ID: 213456 · Promis Medical Australia Pty Ltd · Pro MIS Medical Sytems GmbH · Class I · Started August 21, 2013
Good Name: Promis Medical Australia Pty Ltd - Endotherapy guidewire, reusable
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General-Export
- ARTG ID
- 213456
- Start Date
- August 21, 2013
- Effective Date
- August 21, 2013
- Country
- Germany
- Address
- Theodor-Storm Strasse 33b, Quickborn, 25451
An endotherapy device used in combination with a compatible flexible endoscope to assist in the insertion of an endoscope or endotherapy devices.
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.