Urethral Dilation Set - ANVISA Registration 10150470129

Access comprehensive regulatory information for Urethral Dilation Set in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10150470129 and manufactured by WILLY RUSCH AG. The registration is held by CIRURGICA FERNANDES - COMERCIO DE MATERIAIS CIRURGICOS E HOSPITALARES - SOCIEDADE LIMITADA 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 AMECO MEDICAL INDUSTRIES, BOSTON SCIENTIFIC CORPORATION, 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.