LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM - ANVISA Registration 81086970009

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 III medical device is registered under ANVISA number 81086970009 and manufactured by INOMED MIDIZINTECHNIK GMBH. The registration is held by rbtg brasil equipamentos médicos hospitalares ltda with validity until Jul 11, 2026.

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.