HONIGUM® LIGHT FAST IMPRESSION MATERIAL - FDA Registration MDR-04873B

Access comprehensive regulatory information for HONIGUM® LIGHT FAST IMPRESSION MATERIAL in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04873B and manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH in Germany. The device was registered on October 24, 2017.

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.