SPINAL FUSION CAGES - ANVISA Registration 80071910131

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 80071910131 and manufactured by OSTEOMED S.A. The registration is held by OSTEOMED S.A with validity until Jun 30, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including AESCULAP AG, MEDACTA INTERNATIONAL 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.