Blood Centrifuge - ANVISA Registration 82251719008

Access comprehensive regulatory information for Blood 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 82251719008 and manufactured by ACCUMAX LAB DEVICES PRIVATE LIMITED. The registration is held by SMITH KLIMB COMÉRCIO IMPORTAÇÃO DE PRODUTOS HOSPITALARES 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 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.