Electric infusion pump administration set
Australia TGA ARTG Registered Device · Bayer Australia Ltd · Bayer AG · Class IIa · Started May 11, 2021
Good Name: Bayer Australia Ltd - Electric infusion pump administration set
- Risk Class
- Class IIa
- Product Type
- Procedure Pack
- ARTG Category
- General
- Start Date
- May 11, 2021
- Effective Date
- May 11, 2021
- Name
- Bayer AG
- Country
- Germany
- Address
- Kaiser-Wilhelm-Allee, Bayerwerk, Leverkusen, 51368
Perfusion tube for administering infusion solution
Access comprehensive regulatory information for Electric infusion pump administration set in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Bayer Australia Ltd, manufactured by Bayer AG in Germany. The device registration started on May 11, 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.