Nidek Medical Oxygen Concentrators - EUDAMED Registration 00038214000974

Access comprehensive regulatory information for Nidek Medical Oxygen Concentrators in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 00038214000974 and manufactured by Nidek Medical Products Inc. in United States.

This page provides complete registration details including trade name (Mark 5 Nuvo Lite), manufacturer information, authorized representative details, competent authority (DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover), 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.