Rigid Endoscope - ANVISA Registration 81595559011

Access comprehensive regulatory information for Rigid Endoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81595559011 and manufactured by ARTHIMED USA LLC. The registration is held by MF MEDICAL - LTDA - ME 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 RICHARD WOLF GMBH, OLYMPUS WINTER & IBE 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.