PNEUMOCYSTIS - ANVISA Registration 80502070109
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 80502070109 and manufactured by CERTEST BIOTEC, S.L.. The registration is held by MOBIUS LIFE SCIENCE INDUSTRIA E COMERCIO DE PRODUTOS PARA LABORATORIOS 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, 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.
Device Details
Registration Details
80502070109
25351356365202331
04645160000149
Company Information
Dates and Status
Jul 03, 2023
VIGENTE
09/18/2025 19:00:01
PNEUMOCYSTIS
Pneumocystis ELITe MGBยฎ Kit
ELITECH GROUP S.P.A
80686360385
Aug 14, 2023
PNEUMOCYSTIS
Famรญlia de Detecรงรฃo PCR em tempo real VIASURE Pneumocystis jirovecii
CERTEST BIOTEC, S.L.
10355870361
Jan 20, 2020
PNEUMOCYSTIS
MERIFLUOR PNEUMOCISTIS
MERIDIAN BIOSCIENCE
10230730050
Apr 05, 2005

