Glenoid component for shoulder arthroplasty - ANVISA Registration 10132590614

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 III medical device is registered under ANVISA number 10132590614 and manufactured by DEPUY IRELAND UC. The registration is held by JOHNSON & JOHNSON DO BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDA with validity until Feb 13, 2026.

This page provides complete technical specifications for 3 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.

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10132590614
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Registration Details
ANVISA Registration Number: 10132590614
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Related Devices (3)

COMPONENTE GLENOIDE PARA PROTESE DE OMBRO GLOBAL
Risk Class III

Registration Details

10132590614

250000090859854

54516661000101

Company Information

DEPUY IRELAND UC
Ireland
PT: IRLANDA

Dates and Status

Feb 13, 2001

13/02/2026

09/18/2025 19:00:01

COMPONENTE GLENOIDE PARA PROTESE DE OMBRO GLOBAL
Risk Class III

Registration Details

10132590614

250000090859854

54516661000101

Dates and Status

Feb 13, 2001

13/02/2026

09/18/2025 19:00:01

COMPONENTE GLENOIDE PARA PROTESE DE OMBRO GLOBAL
Risk Class III

Registration Details

10132590614

250000090859854

54516661000101

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 13, 2001

13/02/2026

09/18/2025 19:00:01