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Endotherapy overtube, reusable - ARTG 213457

Access comprehensive regulatory information for Endotherapy overtube, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 213457 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.

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Class I
ARTG 213457
Class I
Endotherapy overtube, reusable
ARTG ID: 213457
Good Name: Promis Medical Australia Pty Ltd - Endotherapy overtube, reusable
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Intended Purpose

An endotherapy device intended to aid in endoscopic insertions secure a pathway for multiple endoscopic intubations during diagnostic and therapeutic endoscopy.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General-Export
Registration Information
ARTG ID
213457
Start Date
August 21, 2013
Effective Date
August 21, 2013
Manufacturer
Country
Germany
Address
Theodor-Storm Strasse 33b, Quickborn, 25451