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INTRACRANIAL STENT - ANVISA Registration 80005430444

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 80005430444 and manufactured by Stryker Neurovascular. The registration is held by STRYKER DO BRASIL LTDA with validity until Nov 21, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BALT EXTRUSION SAS, PHENOX GMBH, 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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80005430444
2 Related Devices
Registration Details
ANVISA Registration Number: 80005430444
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Related Devices (2)

Surpass Streamline Dispositivo Redirecionador de Fluxo
Risk Class IV

Registration Details

80005430444

25351384999201657

02966317000102

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Nov 21, 2016

21/11/2026

09/18/2025 19:00:01

Surpass Streamline Dispositivo Redirecionador de Fluxo
Risk Class IV

Registration Details

80005430444

25351384999201657

02966317000102

Company Information

Dates and Status

Nov 21, 2016

21/11/2026

09/18/2025 19:00:01