FIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP) - ANVISA Registration 80003610521

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 80003610521 and manufactured by BIOKIT S/A. The registration is held by WERFEN MEDICAL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 4 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.