Respirometer - ANVISA Registration 80975350001

Access comprehensive regulatory information for Respirometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80975350001 and manufactured by KOKO, LLC. The registration is held by AAMED COMÉRCIO DE EQUIPAMENTOS 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 TELEFLEX MEDICAL, ANESTHESIA ASSOCIATES, INC., 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.