PLASMA DEFICIENT IN COAGULATION FACTORS - ANVISA Registration 80049120100

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 80049120100 and manufactured by ALAMAR TECNO CIENTÍFICA LTDA. The registration is held by ALAMAR TECNO CIENTÍFICA 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 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.