Australia flagARTG 472646

Sponge, ophthalmic

ARTG ID: 472646 · Ophthalmopro Pty Ltd · PSI/EYE-KO INC dba Anodyne Surgical · Class Is · Started December 11, 2024

Good Name: Ophthalmopro Pty Ltd - Sponge, ophthalmic

Device classification
Risk Class
Class Is
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
472646
Start Date
December 11, 2024
Effective Date
December 11, 2024
Sponsor
Manufacturer
Country
United States of America
Address
804 Corporate Centre Drive, O'Fallon, Missouri USA, 63368
Intended purpose

A device for use in ophthalmic or microscopic surgical procedures for absorbing excess fluids from the operative field.

About this record

Access comprehensive regulatory information for Sponge, ophthalmic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Is is registered under ARTG number 472646 and sponsored by Ophthalmopro Pty Ltd, manufactured by PSI/EYE-KO INC dba Anodyne Surgical in United States of America. The device registration started on December 11, 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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