Denture Reline Acrylic - EUDAMED Registration D6500920P10

Access comprehensive regulatory information for Denture Reline Acrylic in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI D6500920P10 and manufactured by Lang Dental Manufacturing Company, Inc. in United States.

This page provides complete registration details including trade name (FLEXACRYL), manufacturer information, authorized representative details, competent authority (Agence Nationale de Sécurité du Médicament et des Produits de Santé), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.