HP PTA Balloon Catheter - EUDAMED Registration 06971971810520

Access comprehensive regulatory information for HP PTA Balloon Catheter 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 06971971810520 and manufactured by Zhejiang Zylox Medical Device Co., Ltd. in China.

This page provides complete registration details including trade name (ZENFLOW), manufacturer information, authorized representative details, competent authority (DE/CA05 - Behorde fur Justiz und Verbraucherschutz), 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.