INTRACRANIAL STENT - ANVISA Registration 80583400008

Access comprehensive regulatory information for INTRACRANIAL STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80583400008 and manufactured by manufacturer not specified. The registration is held by ENDOTEC PRODUTOS MEDICOS S/A with validity until Aug 10, 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 BALT EXTRUSION SAS, Stryker Neurovascular, 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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80583400008
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Registration Details
ANVISA Registration Number: 80583400008
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

STENT FRED - DISPOSITIVO ENDOLUMINAL DE REDIRECIONAMENTO DE FLUXO
Risk Class IV

Registration Details

80583400008

25351588208201826

09586279000101

Company Information

Dates and Status

Sep 03, 2018

10/08/2035

09/18/2025 19:00:01

STENT FRED - DISPOSITIVO ENDOLUMINAL DE REDIRECIONAMENTO DE FLUXO
Risk Class IV

Registration Details

80583400008

25351588208201826

09586279000101

Company Information

France
PT: FRANÇA

Dates and Status

Sep 03, 2018

10/08/2035

09/18/2025 19:00:01