Philippines FDA registration MDR-01719

IPS Empress® Direct Color Composite Resin Refill

Philippines flagPhilippines·Ivoclar Vivadent AG - Bendererstrasse 2. FL-9494 Schaan Principality of Liechtenstein·Liechtenstein·Issued May 26, 2025 – January 15, 2030
Device information
Product Name
IPS Empress® Direct Color Composite Resin Refill
Registration Number
MDR-01719
Manufacturer details
Country of Origin
Liechtenstein
Importer & distribution
Importer/Distributor
Alphadent Corporation
Registration dates
Issuance Date
May 26, 2025
Expiry Date
January 15, 2030
About this record

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.

Free DatabasePowered by Pure Global AIFDA Official DataLiechtenstein