SPINAL FUSION CAGES - ANVISA Registration 80454380102

Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80454380102 and manufactured by SPINEWAY SA. The registration is held by ORTOSPINE COMERCIO IMPORTACAO E EXPORTACAO DE MATERIAL HOSPITALAR LTDA. with validity until May 20, 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.