Papillotome - ANVISA Registration 80050030110

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 80050030110 and manufactured by manufacturer not specified. The registration is held by GASTRO COMÉRCIO E REPRESENTAÇÕES COMERCIAIS DE EQUIPAMENTOS MEDICO HOSPITALARES LTDA with validity until Jun 13, 2026.

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.