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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 IIa is sponsored by Spectrum Surgical Pty Ltd, manufactured by France Chirurgie Instrumentation SAS (FCI S.A.S) in France. The device registration started on July 29, 2021.

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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Class IIa
Class IIa
Vitreoretinal tamponade tubing
Australia TGA ARTG Registered Device
Good Name: Spectrum Surgical Pty Ltd - Vitreoretinal tamponade tubing
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Intended Purpose

A single use and sterile tubing used to connect with an injection device to an instrument that is used to penetrate the ocular orbit for infusion or removal of a tamponade (eg. silicone oil) during surgery of the retinal space. Multiple adaptor connectors are available with which to interface with the device.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
July 29, 2021
Effective Date
July 29, 2021
Manufacturer
Country
France
Address
20-22 rue Louis Armand, Paris, 75015