External Fixation System - ANVISA Registration 80312580003

Access comprehensive regulatory information for External Fixation System in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80312580003 and manufactured by RESPONSE ORTHO TEKNOLOJIK URETIM A S. The registration is held by TECNIMED - COMÉRCIO E IMPORTAÇÃO DE PRODUTOS MÉDICOS E HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including RESPONSE ORTHO TEKNOLOJIK URETIM A S, SELAZ INDÚSTRIA E COMÉRCIO DE APARELHOS BIOMECÂNICOS LTDA, 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.