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INTRACRANIAL STENT - ANVISA Registration 81836600006

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 81836600006 and manufactured by PHENOX GMBH. The registration is held by PHENOX DO BRASIL COMERCIO DE MATERIAS MEDICOS LTDA with validity until Feb 03, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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81836600006
2 Related Devices
Registration Details
ANVISA Registration Number: 81836600006
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Related Devices (2)

Stent Diversor de Fluxo p64 MW
Risk Class IV

Registration Details

81836600006

25351872546202319

33038158000100

Company Information

PHENOX GMBH
Germany
PT: ALEMANHA

Dates and Status

Feb 03, 2025

03/02/2035

09/18/2025 19:00:01

Stent Diversor de Fluxo p64 MW
Risk Class IV

Registration Details

81836600006

25351872546202319

33038158000100

Company Information

Dates and Status

Feb 03, 2025

03/02/2035

09/18/2025 19:00:01