Centrifuge - ANVISA Registration 10301169005

Access comprehensive regulatory information for Centrifuge in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10301169005 and manufactured by SAKURA FINETEK USA, INC.. The registration is held by BIODINA INSTRUMENTOS CIENTIFICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.