Evolut™ FX Transcatheter Aortic Valve - FDA Registration CMDR-2025-04902A

Access comprehensive regulatory information for Evolut™ FX Transcatheter Aortic Valve in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04902A and manufactured by Medtronic International Limited. - 49 Changi South Avenue 2 Singapore Mfd. By: Medtronic Mexico S. de R.L. de CV - Av. Paseo Cucapah, 10510 El Lago, C.P. 22210 Tijuana, Baja California, Mexico For: Medtronic CoreValve LLC - 1851 E. Deere Avenue, Santa Ana, CA 92705, USA in Mexico. The device was registered on June 17, 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.