Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass. - ANVISA Registration 80218010015

Access comprehensive regulatory information for Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass. in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80218010015 and manufactured by SPINEVISION S.A. The registration is held by ORTOMEDIC DISTRIBUIDORA DE PRODUTOS MEDICOS LTDA with validity until Jul 07, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ORTHOFIX INC., NEOORTHO PRODUTOS ORTOPÉDICOS S/A, 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.