COMPANION DIAGNOSTICS - ANVISA Registration 10287411301

Access comprehensive regulatory information for COMPANION DIAGNOSTICS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10287411301 and manufactured by VENTANA MEDICAL SYSTEM, INC. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until Feb 14, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including ROCHE DIAGNOSTICS GMBH, VENTANA MEDICAL SYSTEM, INC, 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.