Centrifuge - ANVISA Registration 80430569003

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 80430569003 and manufactured by SPINLAB CO. The registration is held by EXIMLAB COMERCIO DE EQUIPAMENTOS PARA LABORATORIOS 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.