Australia TGA ARTG record

Dilator, vaginal

Australia TGA ARTG Registered Device · Profile Medical Devices Pty Ltd · Kessel medintim GmbH · Class I · Started March 17, 2021

Good Name: Profile Medical Devices Pty Ltd - Dilator, vaginal

Device classification

Risk Class: Class I
Product Type: Procedure Pack
ARTG Category: General

Registration information

Start Date: March 17, 2021
Effective Date: March 17, 2021

Sponsor

Name: Profile Medical Devices Pty Ltd

Manufacturer

Name: Kessel medintim GmbH
Country: Germany
Address: Kelsterbacher Strasse 28, Moerfelden-Walldorf, 64546

Intended purpose

Vaginal dilators for dyspareunia, vaginismus, post gynaecological procedures, during and after radiotherapy/chemotherapy.

About this record

Access comprehensive regulatory information for Dilator, vaginal in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Profile Medical Devices Pty Ltd, manufactured by Kessel medintim GmbH in Germany. The device registration started on March 17, 2021.

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.