HEMOGLOBIN SELF-TEST INSTRUMENT - ANVISA Registration 82202950021

Access comprehensive regulatory information for HEMOGLOBIN SELF-TEST INSTRUMENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82202950021 and manufactured by MICO BIOMED CO., LTD.. The registration is held by MICO BIOMED DO 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.