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Vaginal applicators - Medicine administration kit, <specify> - ARTG 132046

Access comprehensive regulatory information for Vaginal applicators - Medicine administration kit, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 132046 and sponsored by Bayer Australia Ltd, manufactured by Manfred Schagner GmbH in Germany. The device registration started on October 09, 2006.

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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TGA ARTG Official Data
Class I
ARTG 132046
Class I
Vaginal applicators - Medicine administration kit, <specify>
ARTG ID: 132046
Good Name: Bayer Australia Limited - Vaginal applicators - Medicine administration kit, <specify>
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Intended Purpose

Used in the treatment of the vagina by the application of a medication agent. The device is a simple rod or blade which is supplied with the medicine for single or multiple use and is disposable after use.

Device Classification
Risk Class
Class I
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
132046
Start Date
October 09, 2006
Effective Date
October 09, 2006
Manufacturer
Country
Germany
Address
Industriestrasse 3, Steinmauern, 76479