INTRACRANIAL STENT - ANVISA Registration 81836600005

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 81836600005 and manufactured by PHENOX GMBH. The registration is held by PHENOX DO BRASIL COMERCIO DE MATERIAS MEDICOS LTDA with validity until Jan 27, 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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81836600005
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Registration Details
ANVISA Registration Number: 81836600005
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Stent Diversor de Fluxo p48 MW HPC
Risk Class IV

Registration Details

81836600005

25351904012202431

33038158000100

Company Information

PHENOX GMBH
Germany
PT: ALEMANHA

Dates and Status

Jan 27, 2025

27/01/2035

09/18/2025 19:00:01

Stent Diversor de Fluxo p48 MW HPC
Risk Class IV

Registration Details

81836600005

25351904012202431

33038158000100

Company Information

Dates and Status

Jan 27, 2025

27/01/2035

09/18/2025 19:00:01