TOXO Toxoplasma Antibody IgG Rapid Test Kit (Colloidal Gold) - EUDAMED Registration 06935091671768

Access comprehensive regulatory information for TOXO Toxoplasma Antibody IgG Rapid Test Kit (Colloidal Gold) in the European Union medical device market through Pure Global AI's free database. This IVD Annex II List B device is registered with EU EUDAMED under Primary DI 06935091671768 and manufactured by Qingdao Hightop Biotech Co., Ltd. in China.

This page provides complete registration details including trade name (TOXO Toxoplasma Antibody IgG Rapid Test Kit (Colloidal Gold)), 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.