Flexible Endoscope - ANVISA Registration 10371280048

Access comprehensive regulatory information for Flexible 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 10371280048 and manufactured by PENTAX - AOHUA MEDICAL TECHNOLOGIES CO., LTD.. The registration is held by PENTAX MEDICAL BRASIL MATERIAIS E EQUIPAMENTOS LTDA - EPP 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 FUJIFILM CORPORATION, OLYMPUS MEDICAL SYSTEMS CORP., 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.