Software - ANVISA Registration 80753460050

Access comprehensive regulatory information for Software in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80753460050 and manufactured by KARL STORZ SE & CO. KG. The registration is held by KARL STORZ ENDOSCOPIA BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details. 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.