ARTG 292391Medicine administration kit, percutaneous, medicated, single-use
ARTG ID: 292391 · Pfizer Australia Pty Ltd · Pfizer Manufacturing Belgium · Class IIa · Started August 03, 2017
Good Name: Pfizer Australia Pty Ltd - Medicine administration kit, percutaneous, medicated, single-use
- Risk Class
- Class IIa
- Product Type
- Procedure Pack
- ARTG Category
- General
- ARTG ID
- 292391
- Start Date
- August 03, 2017
- Effective Date
- August 03, 2017
- Country
- Belgium
- Address
- Rijksweg 12, Puurs-Sint-Amands, 2870
A collection of items used to administer a medication by injection. It contains vials of the medicine, diluent syringes and injection needles. These are single use injections.
Access comprehensive regulatory information for Medicine administration kit, percutaneous, 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 292391 and sponsored by Pfizer Australia Pty Ltd, manufactured by Pfizer Manufacturing Belgium in Belgium. The device registration started on August 03, 2017.
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.