Catheter Fixation Device - ANVISA Registration 80022069036
Access comprehensive regulatory information for Catheter Fixation Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80022069036 and manufactured by FUJIFILM MEDWORK GMBH. The registration is held by FUJIFILM DO BRASIL LTDA with validity until currently active (VIGENTE).
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 PHARMAPLAST S.A.E, BARD ACCESS SYSTEMS, INC., 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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Registration Details
80022069036
25351323288202414
60397874000156
Company Information
Dates and Status
Jun 17, 2024
VIGENTE
09/18/2025 19:00:01
INTRAVASCULAR GUIDE CATHETER
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80740950012
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Devices
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Guide Wire
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Guide Wire
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Catheter Introducer Guide
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10289680094
Aug 17, 2015
PHARMAPLAST S.A.E• Egypt
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MDL ARTIGOS HOSPITALARES E LABORATORIAIS LTDA ME• Brazil
3M COMPANY• United States of America
TIDI PRODUCTS, LLC• United States of America
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