REBOA - EUDAMED Registration D-10887714022040NH

Access comprehensive regulatory information for REBOA in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI D-10887714022040NH and manufactured by NuMED, Inc. in United States.

This page provides complete registration details including trade name (REBOA), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.