Advisa DR MRI™ SureScan™ Digital Dual Chamber Pacemaker with Surescan Technology - FDA Registration MDR-01732

Access comprehensive regulatory information for Advisa DR MRI™ SureScan™ Digital Dual Chamber Pacemaker with Surescan Technology in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01732 and manufactured by Medtronic International Limited- 50 Pasir Panjang Road, #04-51 Mapletree Business City, Singapore Mfd by: Medtronic Europe Sàrl – Route du Molliau 31, Case Postale, 1131 Tolochenaz, Switzerland Mfd for: Medtronic, Inc. -710 Medtronic Parkway Minneapolis, MN 55432 USA in USA. The device was registered on February 19, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Medtronic Philippines, Inc), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.