3M ESPE FILTEK BULK FILL POSTERIOR RESTORATIVE - FDA Registration MDR-03511

Access comprehensive regulatory information for 3M ESPE FILTEK BULK FILL POSTERIOR RESTORATIVE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-03511 and manufactured by 3M Espe Dental Products - Minnesota, USA in USA. The device was registered on October 01, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (3M 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.