Australia TGA ARTG record

Speculum, eye

Australia TGA ARTG Registered Device · Bausch & Lomb Australia Pty Ltd · Bausch & Lomb Inc · Class I · Started September 21, 2022

Good Name: Bausch & Lomb Australia Pty Ltd - Speculum, eye

Device classification

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

Registration information

Start Date: September 21, 2022
Effective Date: September 21, 2022

Sponsor

Name: Bausch & Lomb Australia Pty Ltd

Manufacturer

Name: Bausch & Lomb Inc
Country: United States of America
Address: 1400 North Goodman Street, Rochester, New York, 14609

Intended purpose

A reusable surgical instrument for expanding or stretching the tissue around the eye cavity when inserted and opened. It is used for examination or during ophthalmic surgery. It is usually made of stainless steel with a self-opening or adjustable mechanism.

About this record

Access comprehensive regulatory information for Speculum, eye in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Bausch & Lomb Australia Pty Ltd, manufactured by Bausch & Lomb Inc in United States of America. The device registration started on September 21, 2022.

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.