Subcutaneous Infusion Catheter - ANVISA Registration 80991380020

Access comprehensive regulatory information for Subcutaneous Infusion Catheter in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80991380020 and manufactured by K.F.F. S.A. The registration is held by DR IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including UNOMEDICAL A/S, and 1 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.