Graft-carrying diaphyseal spacer cage - ANVISA Registration 80218010017

Access comprehensive regulatory information for Graft-carrying diaphyseal spacer cage in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80218010017 and manufactured by SPINEVISION S.A. The registration is held by ORTOMEDIC DISTRIBUIDORA DE PRODUTOS MEDICOS LTDA with validity until Jul 14, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 1 companies making the same product including SPINEVISION S.A, and 2 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.