Airflow Cannula - EUDAMED Registration B14003040

Access comprehensive regulatory information for Airflow Cannula in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI B14003040 and manufactured by BRAEBON Medical Corporation in Canada.

This page provides complete registration details including trade name (Male to Barb Tubing), 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.