Endoscopic Instruments - ANVISA Registration 81595550016

Access comprehensive regulatory information for Endoscopic Instruments in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81595550016 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, RZ 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.