ARTG 484107Lens, intraocular, posterior chamber
ARTG ID: 484107 · Kevin Grundy (IBD) Pty Ltd · Lifeline Medical Devices Pvt Ltd · Class IIb · Started March 26, 2025
Good Name: Kevin Grundy (IBD) Pty Ltd - Lens, intraocular, posterior chamber
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 484107
- Start Date
- March 26, 2025
- Effective Date
- March 26, 2025
- Country
- India
- Address
- Plot No D-187/13 Shendra MIDC Area Shendra, Aurangabad, Maharashtra, 431154
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.
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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