Pupillometer - ANVISA Registration 80991380081

Access comprehensive regulatory information for Pupillometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80991380081 and manufactured by KFF S.A. The registration is held by DR IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO 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 TAIZHOU WENBANG TECHNOLOGY DEVELOPMENT CO, .LTD., SEAGULL CAMERA CO LTD., 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.