HEMOGLOBIN SUBTYPE - NEONATAL SCREENING - ANVISA Registration 81733730001

Access comprehensive regulatory information for HEMOGLOBIN SUBTYPE - NEONATAL SCREENING in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81733730001 and manufactured by TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA. The registration is held by TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA with validity until May 20, 2029.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 3 companies making the same product including WALLAC OY, SEBIA, 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.