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INTRACRANIAL STENT - ANVISA Registration 81936210016

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 81936210016 and manufactured by BALT EXTRUSION SAS. The registration is held by BALT BRASIL PRODUTOS MEDICOS LTDA with validity until Jun 23, 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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81936210016
2 Related Devices
Registration Details
ANVISA Registration Number: 81936210016
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Related Devices (2)

STENT SILK
Risk Class IV

Registration Details

81936210016

25351040743202104

12236355000244

Company Information

BALT EXTRUSION SAS
France
PT: FRANร‡A

Dates and Status

Mar 22, 2021

23/06/2035

09/18/2025 19:00:01

STENT SILK
Risk Class IV

Registration Details

81936210016

25351040743202104

12236355000244

Company Information

Dates and Status

Mar 22, 2021

23/06/2035

09/18/2025 19:00:01