Disposable Amniotic Membrane Rupturer - ANVISA Registration 10237610199

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 10237610199 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, 5 companies making the same product including KYJ Medical Products Co., Ltd., YANCHENG HUIDA MEDICAL INSTRUMENTS CO. LTD, 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.