Lens, intraocular, posterior chamber - ARTG 484107
Access comprehensive regulatory information for Lens, intraocular, posterior chamber in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 484107 and sponsored by Kevin Grundy (IBD) Pty Ltd, manufactured by Lifeline Medical Devices Pvt Ltd in India. The device registration started on March 26, 2025.
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Intended to be placed in the posterior chamber of the Eye replacing the Cataractous natural human lens. The placement allows the lens to function as a refractive medium in the visual correction of Aphakia.