Instrumental for Spine Implant - ANVISA Registration 80505620005

Access comprehensive regulatory information for Instrumental for Spine Implant in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80505620005 and manufactured by BAUI BIOTECH CO., LTD. The registration is held by ARTEMED COMERCIO DE PRODUTOS PARA SAUDE LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MEDTRONIC SOFAMOR DANEK USA, INC., ALPHATEC SPINE INC., 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.