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Connection line - Vitreoretinal tamponade tubing

Australia TGA ARTG Registered Device · Beaver-Visitec International Australia Pty Ltd · Arcadophta SARL · Class IIa · Started July 18, 2018

Good Name: Beaver-Visitec International Australia Pty Ltd - Connection line - Vitreoretinal tamponade tubing

Device classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration information
Start Date
July 18, 2018
Effective Date
July 18, 2018
Sponsor
Manufacturer
Country
France
Address
11 rue Antoine Ricord, Toulouse, 31100
Intended purpose

A single-use connection kit used to join injection equipment with a delivery instrument for intraocular infusion during vitreoretinal surgery.

About this record

Access comprehensive regulatory information for Connection line - Vitreoretinal tamponade tubing in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Beaver-Visitec International Australia Pty Ltd, manufactured by Arcadophta SARL in France. The device registration started on July 18, 2018.

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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