Trochars - ANVISA Registration 80170289012

Access comprehensive regulatory information for Trochars in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80170289012 and manufactured by FRANCE CHIRURGIE INSTRUMENTATION SAS (FCI S.A.S). The registration is held by VISIONMED EQUIPAMENTOS MEDICOS 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 AESCULAP AG, KARL STORZ SE & CO. KG, 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.