Esophageal Dilators - ANVISA Registration 10334789008

Access comprehensive regulatory information for Esophageal Dilators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10334789008 and manufactured by DIVERSATEK HEALTHCARE INC.. The registration is held by G.F.E. DO BRASIL LTDA. 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 JIANGSU VEDKANG MEDICAL SCIENCE AND TECHNOLOGY CO., LTD, DIVERSATEK HEALTHCARE INC., 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.