Instrumentation For Endoscopy - ANVISA Registration 10259750023

Access comprehensive regulatory information for Instrumentation For Endoscopy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10259750023 and manufactured by United States Endoscopy Group, Inc. (US Endoscopy). The registration is held by STERIS SOLUTIONS DO BRASIL IMPORTACAO E COMERCIALIZACAO DE PRODUTOS DA SAUDE LTDA. 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, GETSCH UND HILLER MEDIZINTECHNIK GMBH, 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.