SARS-CoV-2 & Influenza AB Antigen Combo Rapid Test Kit (LFIA) - EUDAMED Registration D-WI-MICR-C83A-25BP

Access comprehensive regulatory information for SARS-CoV-2 & Influenza AB Antigen Combo Rapid Test Kit (LFIA) 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-WI-MICR-C83A-25BP and manufactured by Zhejiang Wantaifu Biotechnology Co., Ltd in China.

This page provides complete registration details including trade name (Bio·Firm), manufacturer information, authorized representative details, competent authority (DE/CA24 - Regierungspräsidium Darmstadt Abteilung Arbeitsschutz und Umwelt), 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.