Catheter Fixation Device - ANVISA Registration 80208360058

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 80208360058 and manufactured by TIDI® Products, LLC. The registration is held by HEMOCAT COMERCIO E IMPORTACAO 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.