Instrumentation For Endoscopy - ANVISA Registration 81000039007

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 81000039007 and manufactured by SHENYANG SHENDA ENDOSCOPE CO., LTD. (BEIDAYING STREET). The registration is held by Autentica Medical Importação Comercio e Serviços LTDA-ME 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 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.