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Ophthalmic cannula, irrigation/aspiration, non-illumiating, single-use - ARTG 453008

Access comprehensive regulatory information for Ophthalmic cannula, irrigation/aspiration, non-illumiating, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 453008 and sponsored by Kevin Grundy (IBD) Pty Ltd, manufactured by Medicel AG in Switzerland. The device registration started on June 20, 2024.

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
ARTG 453008
Class IIa
Ophthalmic cannula, irrigation/aspiration, non-illumiating, single-use
ARTG ID: 453008
Good Name: Kevin Grundy (IBD) Pty Ltd - Ophthalmic cannula, irrigation/aspiration, non-illumiating, single-use
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Intended Purpose

For use in ophthalmic surgery during phacoemulsification procedures for, - aspiration of post-extraction crystalline lens residue and fluids. - infusion of aqueous humour replacement fluid and irrigation fluid.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
453008
Start Date
June 20, 2024
Effective Date
June 20, 2024
Manufacturer
Country
Switzerland
Address
Dornierstrasse 11, Altenrhein, 9423