Rehabilitation - EUDAMED Registration 00768627510059

Access comprehensive regulatory information for Rehabilitation 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 00768627510059 and manufactured by North Coast Medical Inc. in United States.

This page provides complete registration details including trade name (Achieva), 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.