Australia TGA ARTG record

Intravenous administration set, scalp vein

Australia TGA ARTG Registered Device · Bayer Australia Ltd · Terumo Europe NV · Class IIa · Started January 02, 2008

Good Name: Bayer Australia Limited - Intravenous administration set, scalp vein

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: January 02, 2008
Effective Date: January 02, 2008

Sponsor

Name: Bayer Australia Ltd

Manufacturer

Name: Terumo Europe NV
Country: Belgium
Address: Interleuvenlaan 40, Leuven, 3001

Intended purpose

The purpose of the device is to deliver drug intravenously

About this record

Access comprehensive regulatory information for Intravenous administration set, scalp vein 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 Terumo Europe NV in Belgium. The device registration started on January 02, 2008.

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.