Pure Global

Medicine administration kit, percutaneous, non-medicated, single-use

Access comprehensive regulatory information for Medicine administration kit, percutaneous, non-medicated, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Roche Products Pty Ltd, manufactured by B Braun Melsungen AG in Germany. The device registration started on August 13, 2018.

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
Medicine administration kit, percutaneous, non-medicated, single-use
Australia TGA ARTG Registered Device
Good Name: Roche Products Pty Ltd - Medicine administration kit, percutaneous, non-medicated, single-use
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Intended Purpose

Application kit for subcutaneous injection

Device Classification
Risk Class
Class IIa
Product Type
Procedure Pack
ARTG Category
General
Registration Information
Start Date
August 13, 2018
Effective Date
August 13, 2018
Manufacturer
Country
Germany
Address
Carl Braun Strasse 1, Melsungen, 34212