Australia TGA ARTG recordTubing set, heart-lung bypass
Australia TGA ARTG Registered Device · Terumo Australia Pty Ltd · Terumo Europe NV · Class IIa · Started March 12, 2014
Good Name: Terumo Australia Pty Ltd - Tubing set, heart-lung bypass
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 12, 2014
- Effective Date
- March 12, 2014
- Name
- Terumo Europe NV
- Country
- Belgium
- Address
- Interleuvenlaan 40, Leuven, 3001
A pre-packaged sterile tubing set containing tubing and other items (such as clamps, filters, connectors, oxygenator, reservoir, haemoconcentrator, heat exchanger) used in the extracorporeal circuit during cardiopulmonary (heart-lung) bypass procedures for up to 6 hours
Access comprehensive regulatory information for Tubing set, heart-lung bypass in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Terumo Australia Pty Ltd, manufactured by Terumo Europe NV in Belgium. The device registration started on March 12, 2014.
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.