HISTOCOMPATIBILITY PRODUCTS - HLA SEROLOGICAL : FLOW CYTOMETRY - ANTIBODY STUDY BY FLOW CYTOMETRY - ANVISA Registration 80391910001

Access comprehensive regulatory information for HISTOCOMPATIBILITY PRODUCTS - HLA SEROLOGICAL : FLOW CYTOMETRY - ANTIBODY STUDY BY FLOW CYTOMETRY in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80391910001 and manufactured by IMMUCOR GTI DIAGNOSTICS, INC. The registration is held by PH 7 COMÉRCIO E REPRESENTAÇÕES DE PRODUTOS PARA DIAGNÓSTICOS LTDA with validity until May 18, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including ONE LAMBDA, INC., IMMUCOR GTI DIAGNOSTICS, INC, and 4 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.