INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 81356110001

Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81356110001 and manufactured by FABRICADO POR CORDIS DE MEXICO S.A. DE C.V, MEXICO PARA CORDIS COPORATION. The registration is held by CARDINAL HEALTH DO BRASIL LTDA. with validity until currently active (VIGENTE).

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 TERUMO CORPORATION, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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.