ND Temporary Coping, for bridge, PMMA - FDA Registration CMDR-2025-04292B

Access comprehensive regulatory information for ND Temporary Coping, for bridge, PMMA in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04292B and manufactured by Institut Straumann AG Straumann Villeret SA in Switzerland Switzerland. The device was registered on April 15, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Metro DNC Marketing Corporation), 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.