ARTG 461914LASSOSTAR™ NAV Catheter - Electrophysiology cardiac catheter, single-use
ARTG ID: 461914 · Johnson & Johnson Medical Pty Ltd · Biosense Webster Inc · Class III · Started September 03, 2024
Good Name: Johnson & Johnson Medical Pty Ltd - LASSOSTAR™ NAV Catheter - Electrophysiology cardiac catheter, single-use
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 461914
- Start Date
- September 03, 2024
- Effective Date
- September 03, 2024
- Country
- United States of America
- Address
- 31 Technology Drive Suite 200, Irvine, California, 92618
The catheter is intended only for electrophysiological mapping (stimulation and recording) of cardiac structures. The catheter is also intended to interface with a compatible CARTO™ 3 System for visualization.
Access comprehensive regulatory information for LASSOSTAR™ NAV Catheter - Electrophysiology cardiac catheter, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 461914 and sponsored by Johnson & Johnson Medical Pty Ltd, manufactured by Biosense Webster Inc in United States of America. The device registration started on September 03, 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.