PNEUMOCYSTIS - ANVISA Registration 10355870361

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 10355870361 and manufactured by CERTEST BIOTEC, S.L.. The registration is held by BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including MERIDIAN BIOSCIENCE, CERTEST BIOTEC, S.L., 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.