LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM - ANVISA Registration 80202250039

Access comprehensive regulatory information for LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80202250039 and manufactured by manufacturer not specified. The registration is held by ORTHONEURO COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS S/A with validity until Apr 13, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ABBOTT MEDICAL, DIXI MEDICAL, 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.