ANTIBODY FOR CELIAC DISEASE - ANVISA Registration 80464810846
Access comprehensive regulatory information for ANTIBODY FOR CELIAC DISEASE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810846 and manufactured by GOLD STANDARD DIAGNOSTICS KASSEL GMBH. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ORGENTEC DIAGNOSTIKA GMBH, EUROIMMUN AG, 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.
Device Details
Registration Details
80464810846
25351502331202325
09377976000152
Company Information
Dates and Status
Aug 28, 2023
VIGENTE
09/18/2025 19:00:01
ANTICORPO PARA DOENÇA CELÍACA
Família Autoteste Glúten
ZHEJIANG ORIENT GENE BIOTECH CO., LTD.
80113770055
Sep 15, 2025
ANTICORPO PARA DOENÇA CELÍACA
AESKUCARE® Gluten Related Disorders IgA
AESKU DIAGNOSTICS GMBH & CO. KG
80105220280
Jul 07, 2025
ANTICORPO PARA DOENÇA CELÍACA
Gliadin IgM
GA GENERIC ASSAYS GMBH
80464810926
Jul 07, 2025
ANTICORPO PARA DOENÇA CELÍACA
Família Glúten
IN VITRO DIAGNOSTICA LTDA
10303460561
Jun 30, 2025
ANTICORPO PARA DOENÇA CELÍACA
FAMÍLIA MAGLUMI® IgA Anti-DGP (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
81504790469
Mar 05, 2025

