3M ESPE CLINPRO SEALANT (REFILL SYRINGE) - FDA Registration DVR-6569

Access comprehensive regulatory information for 3M ESPE CLINPRO SEALANT (REFILL SYRINGE) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6569 and manufactured by 3M ESPE Dental Products 2510 Conway Avenue, St. Paul, Minnesota, 55144-1000, United States of America in USA. The device was registered on June 09, 2023.

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.