Australia TGA ARTG record

Cannula, eye, lacrimal

Australia TGA ARTG Registered Device · Intermed Medical Pty Ltd · PSI/EYE-KO INC dba Anodyne Surgical · Class IIa · Started July 06, 2023

Good Name: Intermed Medical Pty Ltd - Cannula, eye, lacrimal

Device classification

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

Registration information

Start Date: July 06, 2023
Effective Date: July 06, 2023

Sponsor

Name: Intermed Medical Pty Ltd

Manufacturer

Name: PSI/EYE-KO INC dba Anodyne Surgical
Country: United States of America
Address: 804 Corporate Centre Drive, O'Fallon, Missouri USA, 63368

Intended purpose

Intended for probing and irrigating the lacrimal ducts.

About this record

Access comprehensive regulatory information for Cannula, eye, lacrimal in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Intermed Medical Pty Ltd, manufactured by PSI/EYE-KO INC dba Anodyne Surgical in United States of America. The device registration started on July 06, 2023.

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.