Disc replacement interbody spacing device - ANVISA Registration 80371250007

Access comprehensive regulatory information for Disc replacement interbody spacing device in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80371250007 and manufactured by bioteck industria, comercio, importação e exportação de implantes bio-absorviveis ltda. The registration is held by bioteck industria, comercio, importação e exportação de implantes bio-absorviveis ltda with validity until Jul 23, 2027.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including GLOBUS MEDICAL INC., SPINEWAY SAS, 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.