Alar Nasal SpO2 Sensors - EUDAMED Registration 20884838097173

Access comprehensive regulatory information for Alar Nasal SpO2 Sensors 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 20884838097173 and manufactured by Philips Medical Systems in United States.

This page provides complete registration details including trade name (Nasal Alar SpO2 Sensor FAST Only, 20/CS), 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.