Monoblock glenoid component for shoulder arthroplasty - ANVISA Registration 80070180062
Access comprehensive regulatory information for Monoblock 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 80070180062 and manufactured by LIMACORPORATE S.P.A. The registration is held by ENOVIS SURGICAL BRASIL LTDA with validity until Dec 11, 2027.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.
Janaina dos Santos de Miranda
馃嚙馃嚪 Brazil Regulatory Expert
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Registration Details
80070180062
25351505358201601
03117039000181
Company Information
Dates and Status
Dec 11, 2017
11/12/2027
09/18/2025 19:00:01
Glenoid component for shoulder arthroplasty
Glen贸ide Metal Back de Ombro SMR
Not specified
80070180059
Oct 30, 2017
Glenoid component for shoulder arthroplasty
Glen贸ide Metal Back de Ombro SMR
LIMACORPORATE S.P.A
80070180059
Oct 30, 2017
Glenoid component for shoulder arthroplasty
Glen贸ide AXIOMA de Ombro SMR
Not specified
80070180061
Dec 11, 2017
Glenoid component for shoulder arthroplasty
Glen贸ide AXIOMA de Ombro SMR
LIMACORPORATE S.P.A
80070180061
Dec 11, 2017
Glenoid component for shoulder arthroplasty
COMPONENTE GLENOIDE PARA PROTESE DE OMBRO GLOBAL
DEPUY IRELAND UC
10132590614
Feb 13, 2001