PLASMA DEFICIENT IN COAGULATION FACTORS - ANVISA Registration 80003610450

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 80003610450 and manufactured by INSTRUMENTATION LABORATORY CO.. The registration is held by WERFEN MEDICAL 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, 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.