PepsinogenⅠ(PGⅠ) & Pepsinogen Ⅱ(PG Ⅱ) Combo Test Kit (Fluorescence Immunochromatographic Assay) - EUDAMED Registration D-K90411-039PQ

Access comprehensive regulatory information for PepsinogenⅠ(PGⅠ) & Pepsinogen Ⅱ(PG Ⅱ) Combo Test Kit (Fluorescence Immunochromatographic Assay) 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-K90411-039PQ and manufactured by SHENZHEN REETOO BIOTECHNOLOGY CO., LTD in China.

This page provides complete registration details including 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.