D-DIMER - ANVISA Registration 81086830022

Access comprehensive regulatory information for D-DIMER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81086830022 and manufactured by VEDALAB. The registration is held by FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until Oct 19, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ROCHE DIAGNOSTICS 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.