Australia TGA ARTG record

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

Australia TGA ARTG Registered Device · Kevin Grundy (IBD) Pty Ltd · Medicel AG · Class IIa · Started June 20, 2024

Good Name: Kevin Grundy (IBD) Pty Ltd - Ophthalmic cannula, irrigation/aspiration, non-illumiating, single-use

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: June 20, 2024
Effective Date: June 20, 2024

Sponsor

Name: Kevin Grundy (IBD) Pty Ltd

Manufacturer

Name: Medicel AG
Country: Switzerland
Address: Dornierstrasse 11, Altenrhein, 9423

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.

About this record

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 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.