ANTI-MULLERIAN HORMONE (AMH) - ANVISA Registration 10033121021

Access comprehensive regulatory information for ANTI-MULLERIAN HORMONE (AMH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10033121021 and manufactured by IMMUNOTECH, A BECKMAN COULTER COMPANY. The registration is held by BECKMAN COULTER DO BRASIL COMÉRCIO E IMPORTAÇÃO DE PRODUTOS DE LABORATÓRIO 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 ROCHE DIAGNOSTICS GMBH, IMMUNOTECH, A BECKMAN COULTER COMPANY, 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.