INTRACRANIAL STENT - ANVISA Registration 81836600005

Access comprehensive regulatory information for INTRACRANIAL STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81836600005 and manufactured by PHENOX GMBH. The registration is held by PHENOX DO BRASIL COMERCIO DE MATERIAS MEDICOS LTDA with validity until Jan 27, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BALT EXTRUSION SAS, Stryker Neurovascular, 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.