Antifogging solution for endoscope - ANVISA Registration 80251140039

Access comprehensive regulatory information for Antifogging solution for endoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80251140039 and manufactured by AMERICAN INSTRUMENTS LTDA - EPP. The registration is held by AMERICAN INSTRUMENTS LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including AMERICAN INSTRUMENTS LTDA - EPP, TECNOCIRURGICA COMERCIO DE MATERIAIS MEDICOS CIRURGICOS E HOSPITALARES 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.