Rectosigmoidoscope - ANVISA Registration 10237610002

Access comprehensive regulatory information for Rectosigmoidoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10237610002 and manufactured by KOLPLAST CI LTDA. The registration is held by KOLPLAST CI LTDA 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 FRADEL-MED IND E COM DE APARELHOS MEDICOS LTDA-ME, 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.