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Sponge, ophthalmic

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.

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TGA ARTG Official Data
Class Is
Class Is
Sponge, ophthalmic
Australia TGA ARTG Registered Device
Good Name: Surgivision Pty Ltd - Sponge, ophthalmic
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Intended Purpose

to absorb fluids from the operative field during ophthalmic surgery.

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
Manufacturer
Country
United States of America
Address
2310 La Mirada Drive, Vista, California, 92081