INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 81248520019

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 81248520019 and manufactured by PENUMBRA, INC. (ALAMEDA, CA). The registration is held by Penumbra Latin America Distribuidora de Equipamentos e Produtos Médicos Ltda with validity until May 11, 2030.

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.