PNEUMOCYSTIS - ANVISA Registration 10230730050

Access comprehensive regulatory information for PNEUMOCYSTIS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10230730050 and manufactured by MERIDIAN BIOSCIENCE. The registration is held by NL COMÉRCIO EXTERIOR LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including CERTEST BIOTEC, S.L., ELITECH GROUP S.P.A, and 3 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.