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TECNIS PureSee™ Toric II IOL with TECNIS SIMPLICITY™ Delivery System - Lens, intraocular, posterior chamber - ARTG 440190

Access comprehensive regulatory information for TECNIS PureSee™ Toric II IOL with TECNIS SIMPLICITY™ Delivery System - Lens, intraocular, posterior chamber in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 440190 and sponsored by AMO Australia Pty Ltd, manufactured by Johnson & Johnson Surgical Vision Inc in United States of America. The device registration started on February 07, 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 III
ARTG 440190
Class III
TECNIS PureSee™ Toric II IOL with TECNIS SIMPLICITY™ Delivery System - Lens, intraocular, posterior chamber
ARTG ID: 440190
Good Name: AMO Australia Pty Ltd - TECNIS PureSee™ Toric II IOL with TECNIS SIMPLICITY™ Delivery System - Lens, intraocular, posterior chamber
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Intended Purpose

The TECNIS PureSee™ Toric II IOL is intended to correct aphakia following removal of the natural crystalline lens.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
440190
Start Date
February 07, 2024
Effective Date
February 07, 2024
Manufacturer
Country
United States of America
Address
31 Technology Drive Suite 200, Irvine CA, 92618