HEMOGLOBIN SUBTYPE - ANVISA Registration 10230730080

Access comprehensive regulatory information for HEMOGLOBIN SUBTYPE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10230730080 and manufactured by HELENA LABORATORIES. The registration is held by NL COMÉRCIO EXTERIOR LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SEBIA, BIO-RAD LABORATORIES 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.