ARTG 4550259F Acuity Pro Guide Catheter - Catheter, intravascular, guiding
ARTG ID: 455025 · Boston Scientific Pty Ltd · Cardiac Pacemakers Inc a subsidiary of Boston Scientific Corporation · Class III · Started July 10, 2024
Good Name: Boston Scientific Pty Ltd - 9F Acuity Pro Guide Catheter - Catheter, intravascular, guiding
- Risk Class
- Class III
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 455025
- Start Date
- July 10, 2024
- Effective Date
- July 10, 2024
- Country
- United States of America
- Address
- 4100 Hamline Avenue North, St Paul, Minnesota, 55112-5798
The ACUITY Pro Lead Delivery System is intended to access the coronary venous system. The ACUITY Pro 9F Guide Catheter serves as a conduit for the delivery of contrast medium and devices, including implantable Boston Scientific coronary venous leads, introduced into the coronary venous system. The guide catheter may be used alone (9F) or in dual catheter delivery (9F with 7F).
Access comprehensive regulatory information for 9F Acuity Pro Guide Catheter - 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 455025 and sponsored by Boston Scientific Pty Ltd, manufactured by Cardiac Pacemakers Inc a subsidiary of Boston Scientific Corporation in United States of America. The device registration started on July 10, 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.