Pure Global

Surgical procedure kit, dental, non-medicated, reusable

Access comprehensive regulatory information for Surgical procedure kit, dental, non-medicated, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Dentafusion Implant Group Pty Ltd, manufactured by Bredent Medical GmbH & Co KG in Germany. The device registration started on June 21, 2024.

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 IIa
Class IIa
Surgical procedure kit, dental, non-medicated, reusable
Australia TGA ARTG Registered Device
Good Name: Dentafusion Implant Group Pty Ltd - Surgical procedure kit, dental, non-medicated, reusable
Pure Global
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Intended Purpose

This is a kit that is intended to be used for Dental/Maxillofacial procedures and contains all the relevant devices required to perform such surgical procedures as required.

Device Classification
Risk Class
Class IIa
Product Type
Procedure Pack
ARTG Category
General
Registration Information
Start Date
June 21, 2024
Effective Date
June 21, 2024
Manufacturer
Country
Germany
Address
Weissenhorner strasse 2, Senden, 89250