Introducers - ANVISA Registration 81248529002

Access comprehensive regulatory information for Introducers in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81248529002 and manufactured by PENUMBRA, INC.. The registration is held by Penumbra Latin America Distribuidora de Equipamentos e Produtos Médicos Ltda with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including BROSMED MEDICAL CO., LTD, SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD, 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.