Incision Device - ANVISA Registration 80290739004

Access comprehensive regulatory information for Incision Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80290739004 and manufactured by SUZHOU FRANKENMAN MEDICAL EQUIPMENT CO., LTD. The registration is held by ENDOTECH COMERCIO IMPORTAÇÃO EXPORTAÇÃO E SERVIÇOS 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 MADHU INSTRUMENTS PVT LTD, ITC-INTERNATIONAL TECHNIDYNE 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.