LOW DENSITY LIPOPROTEIN (LDL) - ANVISA Registration 10287410558

Access comprehensive regulatory information for LOW DENSITY LIPOPROTEIN (LDL) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10287410558 and manufactured by DENKA SEIKEN CO. LTD. NIIGATA FACTORY - JAPÃO PARA ROCHE DIAGNOSTICS GMBH. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ELITECH CLINICAL SYSTEMS SAS, BIOSYSTEMS S.A., 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.