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Artificial Embolization Device - ANVISA Registration 10360810071

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 10360810071 and manufactured by manufacturer not specified. The registration is held by DOC MED COMERCIO IMPORTACAO E EXPORTACAO LTDA with validity until Nov 27, 2033.

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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10360810071
2 Related Devices
Registration Details
ANVISA Registration Number: 10360810071
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Related Devices (2)

MENOX™ - SISTEMA EMBÓLICO LÍQUIDO
Risk Class IV

Registration Details

10360810071

25351034431202315

66877184000180

Company Information

Dates and Status

Nov 27, 2023

27/11/2033

09/18/2025 19:00:01

MENOX™ - SISTEMA EMBÓLICO LÍQUIDO
Risk Class IV

Registration Details

10360810071

25351034431202315

66877184000180

Company Information

India
PT: ÍNDIA

Dates and Status

Nov 27, 2023

27/11/2033

09/18/2025 19:00:01