HISTOCOMPATIBILITY PRODUCTS - COMPLEMENTARY REAGENTS - ANVISA Registration 80391910010
Access comprehensive regulatory information for HISTOCOMPATIBILITY PRODUCTS - COMPLEMENTARY REAGENTS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80391910010 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 currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including ONE LAMBDA, INC., AGILENT TECHNOLOGIES SINGAPORE (INTERNATIONAL) PTE LTD., and 2 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.
Device Details
Registration Details
80391910010
25351431702201609
59920132000184
Company Information
Dates and Status
Jan 02, 2017
VIGENTE
09/18/2025 19:00:01
PRODUTOS PARA HISTOCOMPATIBILIDADE - REAGENTES COMPLEMENTARES
Reagentes Complementares Dako
AGILENT TECHNOLOGIES SINGAPORE (INTERNATIONAL) PTE LTD.
80000230064
Dec 26, 2016
PRODUTOS PARA HISTOCOMPATIBILIDADE - REAGENTES COMPLEMENTARES
FluoroQuench AO/EB
ONE LAMBDA, INC.
80298490108
May 10, 2010

