ClariPulmo - EUDAMED Registration D-88000468PMO-20GUNQ

Access comprehensive regulatory information for ClariPulmo in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI D-88000468PMO-20GUNQ and manufactured by ClariPi Inc. in Republic of Korea.

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