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Artificial Embolization Device - ANVISA Registration 81936210006

Access comprehensive regulatory information for Artificial Embolization Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81936210006 and manufactured by EMBO-FLÜSSIGKEITEN A.G.. The registration is held by BALT BRASIL PRODUTOS MEDICOS LTDA with validity until Aug 15, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ECLIPSE MEDICAL CO, LTD., MICRO THERAPEUTICS, INC. DBA EV3 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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81936210006
2 Related Devices
Registration Details
ANVISA Registration Number: 81936210006
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Related Devices (2)

SQUID - SISTEMA EMBÓLICO LÍQUIDO
Risk Class IV

Registration Details

81936210006

25351040234202173

12236355000244

Company Information

Switzerland
PT: SUÍÇA

Dates and Status

Mar 22, 2021

15/08/2026

09/18/2025 19:00:01

SQUID - SISTEMA EMBÓLICO LÍQUIDO
Risk Class IV

Registration Details

81936210006

25351040234202173

12236355000244

Company Information

Dates and Status

Mar 22, 2021

15/08/2026

09/18/2025 19:00:01