Rectosigmoidoscope - ANVISA Registration 80039960023

Access comprehensive regulatory information for Rectosigmoidoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80039960023 and manufactured by FRADEL-MED IND E COM DE APARELHOS MEDICOS LTDA-ME. The registration is held by FRADEL-MED IND E COM DE APARELHOS MEDICOS LTDA-ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including KOLPLAST CI LTDA, FERRARI INDUSTRIA E COMÉRCIO DE APARELHOS MÉDICOS LTDA, and 3 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.