Cobalt™ XT HF Quad CRT-D MRI SureScan™ Implantable Cardioverter Defibrillator - FDA Registration CMDR-2025-04603

Access comprehensive regulatory information for Cobalt™ XT HF Quad CRT-D MRI SureScan™ Implantable Cardioverter Defibrillator in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04603 and manufactured by Medtronic, Inc. - 710 Medtronic Parkway Minneapolis, MN 55432 USA Mfd by: Medtronic Europe Sàrl - Route du Molliau 31, Case Postale, 1131 Tolochenaz, Switzerland in USA. The device was registered on May 20, 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.