Edwards™ Mitris™ Resilia™ Mitral Valve - FDA Registration CMDR-2024-02670B

Access comprehensive regulatory information for Edwards™ Mitris™ Resilia™ Mitral Valve in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02670B and manufactured by Edwards Lifesciences LLC One Edwards Way, Irvine, CA 92614, USA Mfd By: Edwards Lifesciences (Singapore) Pte. Ltd. 35 Changi North Crescent Singapore 499641, Singapore in USA. The device was registered on April 17, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (RG Meditron, 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.