IPS Empress® Direct Color Composite Resin Refill - FDA Registration MDR-01719

Access comprehensive regulatory information for IPS Empress® Direct Color Composite Resin Refill in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01719 and manufactured by Ivoclar Vivadent AG - Bendererstrasse 2. FL-9494 Schaan Principality of Liechtenstein in Liechtenstein. The device was registered on May 26, 2025.

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