Pure Global

VIVAGLASS® CEM PL SELF-CURING GLASS IONOMER BASED RADIOPAQUE LUTING CEMENT - FDA Registration MDR-01903

Access comprehensive regulatory information for VIVAGLASS® CEM PL SELF-CURING GLASS IONOMER BASED RADIOPAQUE LUTING CEMENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01903 and manufactured by Ivoclar Vivadent AG in Liechtenstein. The device was registered on March 25, 2020.

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 Database
Powered by Pure Global AI
FDA Official Data
Liechtenstein
MDR-01903
VIVAGLASS® CEM PL SELF-CURING GLASS IONOMER BASED RADIOPAQUE LUTING CEMENT
Registered medical device in Philippines
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Information
Product Name
VIVAGLASS® CEM PL SELF-CURING GLASS IONOMER BASED RADIOPAQUE LUTING CEMENT
Registration Number
MDR-01903
Manufacturer Details
Country of Origin
Liechtenstein
Importer & Distribution
Importer/Distributor
Alphadent Corporation
Registration Dates
Issuance Date
March 25, 2020
Expiry Date
March 20, 2025