D-DIMER - ANVISA Registration 80474870166

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 80474870166 and manufactured by QINGDAO HIGHTOP BIOTECH CO.,LTD.. The registration is held by BIOSUL PRODUTOS DIAGNOSTICOS LTDA - ME with validity until Sep 08, 2035.

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