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INTRACRANIAL STENT - ANVISA Registration 81936210025

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 81936210025 and manufactured by BALT EXTRUSION SAS. The registration is held by BALT BRASIL PRODUTOS MEDICOS LTDA with validity until Aug 23, 2031.

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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81936210025
2 Related Devices
Registration Details
ANVISA Registration Number: 81936210025
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Related Devices (2)

STENT SILK VISTA
Risk Class IV

Registration Details

81936210025

25351400606202125

12236355000244

Company Information

BALT EXTRUSION SAS
France
PT: FRANร‡A

Dates and Status

Aug 23, 2021

23/08/2031

09/18/2025 19:00:01

STENT SILK VISTA
Risk Class IV

Registration Details

81936210025

25351400606202125

12236355000244

Company Information

Dates and Status

Aug 23, 2021

23/08/2031

09/18/2025 19:00:01