Influenza A&B Rapid Test Kit - EUDAMED Registration D-SC10101W-1TYA

Access comprehensive regulatory information for Influenza A&B Rapid Test Kit in the European Union medical device market through Pure Global AI's free database. This IVD General device is registered with EU EUDAMED under Primary DI D-SC10101W-1TYA and manufactured by Jiangsu Bioperfectus Technologies Co., Ltd. in China.

This page provides complete registration details including trade name (Influenza A&B Rapid Test Kit), 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.