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Electric infusion pump administration set - ARTG 365410

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 registered under ARTG number 365410 and 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.

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Class IIa
ARTG 365410
Class IIa
Electric infusion pump administration set
ARTG ID: 365410
Good Name: Bayer Australia Ltd - Electric infusion pump administration set
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Intended Purpose

Perfusion tube for administering infusion solution

Device Classification
Risk Class
Class IIa
Product Type
Procedure Pack
ARTG Category
General
Registration Information
ARTG ID
365410
Start Date
May 11, 2021
Effective Date
May 11, 2021
Manufacturer
Country
Germany
Address
Kaiser-Wilhelm-Allee, Bayerwerk, Leverkusen, 51368