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Lens, intraocular, posterior chamber - ARTG 473806

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 473806 and sponsored by AMO Australia Pty Ltd, manufactured by Johnson & Johnson Surgical Vision Inc in United States of America. The device registration started on December 18, 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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TGA ARTG Official Data
Class IIb
ARTG 473806
Class IIb
Lens, intraocular, posterior chamber
ARTG ID: 473806
Good Name: AMO Australia Pty Ltd - Lens, intraocular, posterior chamber
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Intended Purpose

The device is intended to correct aphakia following removal of the natural crystalline lens.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
473806
Start Date
December 18, 2024
Effective Date
December 18, 2024
Manufacturer
Country
United States of America
Address
31 Technology Drive Suite 200, Irvine CA, 92618