Pure Global

Brio IPG Model 6788 - Brain electrical stimulation system, antitremor - ARTG 397012

Access comprehensive regulatory information for Brio IPG Model 6788 - Brain electrical stimulation system, antitremor in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 397012 and sponsored by Abbott Medical Australia Pty Ltd, manufactured by St Jude Medical in United States of America. The device registration started on October 06, 2022.

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 III
ARTG 397012
Class III
Brio IPG Model 6788 - Brain electrical stimulation system, antitremor
ARTG ID: 397012
Good Name: Abbott Medical Australia Pty Ltd - Brio IPG Model 6788 - Brain electrical stimulation system, antitremor
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

The Brio neurostimulation system is intended to deliver low-intensity electrical impulses to specific targets in the brain via leads and associated extensions that are compatible with the Brio system.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
397012
Start Date
October 06, 2022
Effective Date
October 06, 2022
Manufacturer
Country
United States of America
Address
6901 Preston Road, Plano, Texas, 75024