Centrifuge - ANVISA Registration 80153030117

Access comprehensive regulatory information for Centrifuge in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80153030117 and manufactured by ZENITH LAB CO., LTD. The registration is held by MONTSERRAT COMERCIAL IMPORTADORA E EXPORTADORA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including SORVALL, CELM COMPANHIA EQUIPADORA DE LABORATORIOS MODERNOS, and 5 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.