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Vitreoretinal tamponade tubing

Access comprehensive regulatory information for Vitreoretinal tamponade tubing in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Beaver-Visitec International Australia Pty Ltd, manufactured by Arcadophta SARL in France. The device registration started on June 15, 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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TGA ARTG Official Data
Class I
Class I
Vitreoretinal tamponade tubing
Australia TGA ARTG Registered Device
Good Name: Beaver-Visitec International Australia Pty Ltd - Vitreoretinal tamponade tubing
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Intended Purpose

A tubing line intended to connect injection equipment with a delivery instrument to assist with intraocular infusion during a vitreoretinal procedure.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
June 15, 2018
Effective Date
June 15, 2018
Manufacturer
Country
France
Address
11 rue Antoine Ricord, Toulouse, 31100