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VersaCross Transseptal Sheath - Catheter, intravascular, guiding - ARTG 457891

Access comprehensive regulatory information for VersaCross Transseptal Sheath - Catheter, intravascular, guiding in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 457891 and sponsored by Boston Scientific Pty Ltd, manufactured by Baylis Medical Company Inc in Canada. The device registration started on July 31, 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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Class III
ARTG 457891
Class III
VersaCross Transseptal Sheath - Catheter, intravascular, guiding
ARTG ID: 457891
Good Name: Boston Scientific Pty Ltd - VersaCross Transseptal Sheath - Catheter, intravascular, guiding
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Intended Purpose

The VersaCross Transseptal Sheath kit is used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, including the left atrium via transseptal perforation / puncture.

Device Classification
Risk Class
Class III
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
457891
Start Date
July 31, 2024
Effective Date
July 31, 2024
Manufacturer
Country
Canada
Address
5959 Trans-Canada Highway, Montreal, Quebec, H4T 1A1