Instrumentation For Endoscopy - ANVISA Registration 81963410008

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 81963410008 and manufactured by GENESYSMED BRASIL COMERCIO DE PRODUTOS HOSPITALARES LTDA. The registration is held by GENESYSMED BRASIL COMERCIO DE PRODUTOS HOSPITALARES 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 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.