Artificial Embolization Device - ANVISA Registration 10413960241

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 10413960241 and manufactured by SCITECH PRODUTOS MEDICOS SA. The registration is held by SCITECH PRODUTOS MEDICOS SA with validity until Apr 03, 2033.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
10413960241
Registration Details
ANVISA Registration Number: 10413960241
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

EMBOFLOW – SISTEMA EMBÓLICO LÍQUIDO
Risk Class IV

Registration Details

10413960241

25351268058202213

01437707000122

Company Information

Brazil
PT: BRASIL

Dates and Status

Apr 03, 2023

03/04/2033

09/18/2025 19:00:01