Australia TGA ARTG record

Speculum, eye

Australia TGA ARTG Registered Device · InstruMED · InstruMED · Class I · Started July 01, 2018

Good Name: InstruMED - Speculum, eye

Device classification

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

Registration information

Start Date: July 01, 2018
Effective Date: July 01, 2018

Sponsor

Name: InstruMED

Manufacturer

Name: InstruMED
Country: Australia
Address: 245 South Road, Mile End, SA, 5031

Intended purpose

A surgical instrument which comprises two arms joined at a pivot point, and which is available in various sizes, shapes and contours. It has a blunt distal tip and is used 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 InstruMED, manufactured by InstruMED in Australia. The device registration started on July 01, 2018.

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.