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VersaCross RF Wire - Endoscopic electrosurgical electrode, monopolar, single-use

Access comprehensive regulatory information for VersaCross RF Wire - Endoscopic electrosurgical electrode, monopolar, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Boston Scientific Pty Ltd, manufactured by Baylis Medical Company Inc in Canada. The device registration started on June 19, 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.

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TGA ARTG Official Data
Class III
Class III
VersaCross RF Wire - Endoscopic electrosurgical electrode, monopolar, single-use
Australia TGA ARTG Registered Device
Good Name: Boston Scientific Pty Ltd - VersaCross RF Wire - Endoscopic electrosurgical electrode, monopolar, single-use
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Intended Purpose

Indicated for creation of an atrial septal defect in the heart.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
June 19, 2024
Effective Date
June 19, 2024
Manufacturer
Country
Canada
Address
5959 Trans-Canada Highway, Montreal, Quebec, H4T 1A1