Australia TGA ARTG record

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

Australia TGA ARTG Registered Device · AMO Australia Pty Ltd · Johnson & Johnson Surgical Vision Inc · Class III · Started February 07, 2024

Good Name: AMO Australia Pty Ltd - TECNIS PureSee™ Toric II IOL with TECNIS SIMPLICITY™ Delivery System - Lens, intraocular, posterior chamber

Device classification

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

Registration information

Start Date: February 07, 2024
Effective Date: February 07, 2024

Sponsor

Name: AMO Australia Pty Ltd

Manufacturer

Name: Johnson & Johnson Surgical Vision Inc
Country: United States of America
Address: 31 Technology Drive Suite 200, Irvine CA, 92618

Intended purpose

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

About this record

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 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.