CX50 Diagnostic Ultrasound Circular Edition - EUDAMED Registration 00884838098008

Access comprehensive regulatory information for CX50 Diagnostic Ultrasound Circular Edition 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 00884838098008 and manufactured by Philips Ultrasound LLC in United States.

This page provides complete registration details including trade name (CX50 Diamond Select), 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.