LUTEINIZING HORMONE (LH) - ANVISA Registration 82378830021

Access comprehensive regulatory information for LUTEINIZING HORMONE (LH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82378830021 and manufactured by DIRUI INDUSTRIAL CO. LTD. The registration is held by CHINA MEHECO BRASIL COMERCIO E DISTRIBUICAO DE EQUIPAMENTOS E MATERIAIS MEDICOS 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, ABBOTT IRELAND DIAGNOSTICS DIVISION, 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.