Papillotome - ANVISA Registration 81263810012

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 81263810012 and manufactured by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS LTDA. The registration is held by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS LTDA with validity until Jan 27, 2030.

This page provides complete technical specifications for this device, 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.