Glenoid component for shoulder arthroplasty - ANVISA Registration 80070180122

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 80070180122 and manufactured by LIMACORPORATE S.P.A. The registration is held by ENOVIS SURGICAL BRASIL LTDA with validity until Dec 16, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details. 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.