INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 10413960155

Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10413960155 and manufactured by SCITECH PRODUTOS MEDICOS SA. The registration is held by SCITECH PRODUTOS MEDICOS SA with validity until Jan 22, 2027.

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 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.