SPINAL FUSION CAGES - ANVISA Registration 80686360248

Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80686360248 and manufactured by SPINEVISION S.A.S. The registration is held by MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA with validity until Jul 15, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including AESCULAP AG, OSTEOMED 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.