Stryker® Coarse Diamond - FDA Registration CMDR-2025-03776

Access comprehensive regulatory information for Stryker® Coarse Diamond in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03776 and manufactured by Transmedic Pte. Ltd. in Singapore. The device was registered on January 31, 2025.

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