Papillotome - ANVISA Registration 81040530085

Access comprehensive regulatory information for Papillotome in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81040530085 and manufactured by MTW ENDOSKOPIE W. HAAG KG.. The registration is held by PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA ME with validity until Apr 05, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including MEDI-GLOBE GMBH, KOBI MEDIZINTECHNIK GMBH, 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.