Glenoid component for shoulder arthroplasty - ANVISA Registration 80005430647

Access comprehensive regulatory information for Glenoid component for shoulder arthroplasty in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80005430647 and manufactured by TORNIER S.A.S. The registration is held by STRYKER DO BRASIL LTDA with validity until Dec 18, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including LIMACORPORATE S.P.A, DEPUY IRELAND UC, 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.