PLASMA DEFICIENT IN COAGULATION FACTORS - ANVISA Registration 10246810222

Access comprehensive regulatory information for PLASMA DEFICIENT IN COAGULATION FACTORS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10246810222 and manufactured by WIENER LABORATORIOS S.A.I.C. The registration is held by LABORLAB PRODUTOS PARA LABORATÓRIOS LTDA EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH, INSTRUMENTATION LABORATORY CO., 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.