Pure Global

Speculum, <specify> - ARTG 464088

Access comprehensive regulatory information for Speculum, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 464088 and sponsored by Surgivision Pty Ltd, manufactured by Aurora Surgical LLC in United States of America. The device registration started on October 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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class I
ARTG 464088
Class I
Speculum, <specify>
ARTG ID: 464088
Good Name: Surgivision Pty Ltd - Speculum, <specify>
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

To be used for examination or during ophthalmic surgery for expanding or stretching the tissue around the eye cavity.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
464088
Start Date
October 11, 2024
Effective Date
October 11, 2024
Manufacturer
Country
United States of America
Address
780 94th Avenue N Suite 108, St Petersburg, FL, 33702