FIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP) - ANVISA Registration 80291330021

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 80291330021 and manufactured by TEM INNOVATIONS GMBH. The registration is held by SUNMEDCARE COMÉRCIO DE PRODUTOS HOSPITALARES 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.