Esophageal Ultrasound Probe - ANVISA Registration 10371280039

Access comprehensive regulatory information for Esophageal Ultrasound Probe in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10371280039 and manufactured by HOYA CORPORATION. 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 similar products found using AI-powered semantic search, 1 companies making the same product including HOYA CORPORATION, and 1 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.