Papillotome - ANVISA Registration 10212990202

Access comprehensive regulatory information for Papillotome in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10212990202 and manufactured by manufacturer not specified. The registration is held by E TAMUSSINO E CIA LTDA with validity until Feb 21, 2027.

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.