Australia TGA ARTG record

Sponge, ophthalmic

Australia TGA ARTG Registered Device · Surgivision Pty Ltd · Surgistar Inc · Class Is · Started September 11, 2020

Good Name: Surgivision Pty Ltd - Sponge, ophthalmic

Device classification

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

Registration information

Start Date: September 11, 2020
Effective Date: September 11, 2020

Sponsor

Name: Surgivision Pty Ltd

Manufacturer

Name: Surgistar Inc
Country: United States of America
Address: 2310 La Mirada Drive, Vista, California, 92081

Intended purpose

to absorb fluids from the operative field during ophthalmic surgery.

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 sponsored by Surgivision Pty Ltd, manufactured by Surgistar Inc in United States of America. The device registration started on September 11, 2020.

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.