Allure RF PM3222 - Biventricular pacemaker - ARTG 401074
Access comprehensive regulatory information for Allure RF PM3222 - Biventricular pacemaker in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 401074 and sponsored by Abbott Medical Australia Pty Ltd, manufactured by St Jude Medical Cardiac Rhythm Management Division in United States of America. The device registration started on December 14, 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.
The Allure PM3222 is intended for patients who would benefit from resynchronization of the right and left ventricles or have one or more conventional indications for the implantation of a pacemaker. Also AT/AF detection algorithm is indicated for detecting atrial tachyarrhythmias which have been found to be associated with an increased risk of stroke in elderly, hypertensive, pacemaker patients without prior history of AF.