Australia flagARTG 304397

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

Device classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
304397
Start Date
June 15, 2018
Effective Date
June 15, 2018
Sponsor
Manufacturer
Country
France
Address
11 rue Antoine Ricord, Toulouse, 31100
Intended purpose

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

About this record

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.

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