FIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP) - ANVISA Registration 80049120099

Access comprehensive regulatory information for FIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80049120099 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 TEM INNOVATIONS GMBH, DIAGNOSTICA STAGO S.A.S., 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.