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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.

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80502070109
Registration Details
ANVISA Registration Number: 80502070109
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Device Details

FAMรLIA XGEN MASTER PARA DETECร‡รƒO DE PNEUMOCYSTIS JIROVECII
Risk Class II

Registration Details

80502070109

25351356365202331

04645160000149

Company Information

Spain
PT: ESPANHA

Dates and Status

Jul 03, 2023

VIGENTE

09/18/2025 19:00:01