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LASSOSTARโ„ข Circular Mapping Catheter - Electrophysiology cardiac catheter, single-use

Access comprehensive regulatory information for LASSOSTARโ„ข Circular Mapping 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 sponsored by Johnson & Johnson Medical Pty Ltd, manufactured by Biosense Webster Inc in United States of America. The device registration started on October 18, 2021.

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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Class III
Class III
LASSOSTARโ„ข Circular Mapping Catheter - Electrophysiology cardiac catheter, single-use
Australia TGA ARTG Registered Device
Good Name: Johnson & Johnson Medical Pty Ltd - LASSOSTARโ„ข Circular Mapping Catheter - Electrophysiology cardiac catheter, single-use
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Intended Purpose

Indicated for multiple electrode electrophysiological recording and stimulation of the atrial region of the heart. When used in conjunction with a radiofrequency (RF) ablation catheter and a compatible multi-channel generator, the catheter can be used to facilitate ablation of cardiac arrhythmias.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
October 18, 2021
Effective Date
October 18, 2021
Manufacturer
Country
United States of America
Address
31 Technology Drive Suite 200, Irvine, California, 92618