Blood Centrifuge - ANVISA Registration 80380260034

Access comprehensive regulatory information for Blood 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 80380260034 and manufactured by REGEN LAB SA. The registration is held by MEDSYSTEMS COMERCIO, IMPORTACAO E EXPORTACAO LTDA - EPP 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 ANDREAS HETTICH GMBH & CO. KG, SHANGHAI LU XIANGYI CENTRIFUGE INSTRUMENT CO., LTD, 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.