ARTG 457890TorFlex™ Transseptal Guiding Sheath - Catheter, intravascular, guiding
ARTG ID: 457890 · Boston Scientific Pty Ltd · Baylis Medical Company Inc · Class III · Started July 31, 2024
Good Name: Boston Scientific Pty Ltd - TorFlex™ Transseptal Guiding Sheath - Catheter, intravascular, guiding
- Risk Class
- Class III
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 457890
- Start Date
- July 31, 2024
- Effective Date
- July 31, 2024
- Country
- Canada
- Address
- 5959 Trans-Canada Highway, Montreal, Quebec, H4T 1A1
The TorFlex™ Transseptal Guiding 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.
Access comprehensive regulatory information for TorFlex™ Transseptal Guiding 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 457890 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.