Instrumentation For Endoscopy - ANVISA Registration 80393910020

Access comprehensive regulatory information for Instrumentation For Endoscopy in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80393910020 and manufactured by ZHEJIANG TIANSONG MEDICAL INSTRUMENT Co., Ltd. The registration is held by ENDOBRAX COMERCIO, IMPORTAÇÃO E EXPORTAÇÃO DE EQUIPAMENTOS MEDICOS LTDA 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, 5 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, GETSCH UND HILLER MEDIZINTECHNIK GMBH, 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.