Disposable Amniotic Membrane Rupturer - ANVISA Registration 10150479078

Access comprehensive regulatory information for Disposable Amniotic Membrane Rupturer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10150479078 and manufactured by NINGBO FOYOMED MEDICAL INSTRUMENTS CO., LTD.. 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 companies making the same product including KYJ Medical Products Co., Ltd., KOLPLAST CI 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.