External Fixation System - ANVISA Registration 80012450029

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 80012450029 and manufactured by RESPONSE ORTHO LLC. The registration is held by BIOSINTESE HOSPITALAR LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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.