Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass. - ANVISA Registration 80444810041

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 80444810041 and manufactured by BIOMET SPINE LLC. The registration is held by HIGHRIDGE MEDICAL BRASIL LTDA with validity until Feb 06, 2027.

This page provides complete technical specifications for 4 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.