Glenoid component for shoulder arthroplasty - ANVISA Registration 80005430799

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 80005430799 and manufactured by manufacturer not specified. The registration is held by STRYKER DO BRASIL LTDA with validity until Jun 23, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including LIMACORPORATE S.P.A, TORNIER S.A.S, 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.