Flexible intramedullary nail - ANVISA Registration 81163850001

Access comprehensive regulatory information for Flexible intramedullary nail in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81163850001 and manufactured by OCX - IMPLANTES ESPECIALIZADOS LTDA - EPP. The registration is held by OCX - IMPLANTES ESPECIALIZADOS LTDA - EPP with validity until May 02, 2026.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 4 companies making the same product including ORTHOSELECT GMBH, ABIMADE INDÚSTRIA E COMÉRCIO DE PRODUTOS MÉDICOS LTDA, 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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81163850001
Registration Details
ANVISA Registration Number: 81163850001
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Haste Intramedular TITANFLEX OCX
Risk Class III

Registration Details

81163850001

25351639778201508

18747435000160

Company Information

Brazil
PT: BRASIL

Dates and Status

May 02, 2016

02/05/2026

09/18/2025 19:00:01