Flexible Endoscope - ANVISA Registration 81464759046

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 81464759046 and manufactured by SONOSCAPE MEDICAL CORP.. The registration is held by Domo Salute Consultoria Regulatória Ltda with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details. 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.