D-DIMER - ANVISA Registration 10310030192

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 10310030192 and manufactured by WAMA PRODUTOS PARA LABORATORIO LTDA. The registration is held by WAMA PRODUTOS PARA LABORATORIO LTDA with validity until Feb 14, 2028.

This page provides complete technical specifications for this device, 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.