Disposable Arterial Venous Fistula Sets - EUDAMED Registration 06944331090252

Access comprehensive regulatory information for Disposable Arterial Venous Fistula Sets 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 06944331090252 and manufactured by Tianjin Hanaco Medical Co.,Ltd in China.

This page provides complete registration details including trade name ( Disposable Arterial Venous Fistula Sets), manufacturer information, authorized representative details, competent authority (DE/CA22 - Bezirksregierung Münster), 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.