HEMOGLOBIN SUBTYPE - NEONATAL SCREENING - ANVISA Registration 10298910184

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 10298910184 and manufactured by manufacturer not specified. The registration is held by REVVITY DO BRASIL LTDA with validity until Oct 21, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA, 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.