Ureteral Stent - ANVISA Registration 80991389040

Access comprehensive regulatory information for Ureteral Stent in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80991389040 and manufactured by KFF 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, 5 companies making the same product including TELEFLEX MEDICAL, MEDTEC SUPPLIES, INDUSTRIA, IMPORTACAO, EXPORTACAO, DISTRIBUICAO E COMERCIO LTDA, 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.