SPINAL FUSION CAGES - ANVISA Registration 80071910020

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 80071910020 and manufactured by OSTEOMEDICAL PRODUTOS MEDICOS E HOSPITALARES LTDA. The registration is held by OSTEOMED S.A with validity until Feb 26, 2035.

This page provides complete technical specifications for this device, 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.