SPINAL FUSION CAGES - ANVISA Registration 80003890120

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 80003890120 and manufactured by manufacturer not specified. The registration is held by CANADA CENTRAL DE NEGOCIOS DO BRASIL LTDA with validity until Apr 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.