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Medicine administration kit, percutaneous, non-medicated, single-use - ARTG 308170

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 registered under ARTG number 308170 and 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
ARTG 308170
Class IIa
Medicine administration kit, percutaneous, non-medicated, single-use
ARTG ID: 308170
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
ARTG ID
308170
Start Date
August 13, 2018
Effective Date
August 13, 2018
Manufacturer
Country
Germany
Address
Carl Braun Strasse 1, Melsungen, 34212