Catheter Fixation Device - ANVISA Registration 10312210072

Access comprehensive regulatory information for Catheter Fixation Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10312210072 and manufactured by TIDI PRODUCTS, LLC. The registration is held by MEDCORP SAUDE TECNOLOGIA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 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.