Vitreoretinal tamponade tubing
ARTG ID: 304397 · Beaver-Visitec International Australia Pty Ltd · Arcadophta SARL · Class I · Started June 15, 2018
Good Name: Beaver-Visitec International Australia Pty Ltd - Vitreoretinal tamponade tubing
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 304397
- Start Date
- June 15, 2018
- Effective Date
- June 15, 2018
- Name
- Arcadophta SARL
- Country
- France
- Address
- 11 rue Antoine Ricord, Toulouse, 31100
A tubing line intended to connect injection equipment with a delivery instrument to assist with intraocular infusion during a vitreoretinal procedure.
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 registered under ARTG number 304397 and 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.