CELIAC DISEASE ANTIBODY SELF-TEST - ANVISA Registration 80535240072
Access comprehensive regulatory information for CELIAC DISEASE ANTIBODY SELF-TEST in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80535240072 and manufactured by CHEMBIO DIAGNOSTICS BRAZIL LTDA.. The registration is held by CHEMBIO DIAGNOSTICS BRAZIL 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 VEDALAB, BIOSYNEX SA, and 3 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
80535240072
25351400873202445
09449181000102
Company Information
Dates and Status
Dec 23, 2024
VIGENTE
09/18/2025 19:00:01
AUTOTESTE PARA ANTICORPO PARA DOENÇA CELÍACA
Gluten’ Alarm® Homeuse
VEDALAB
80464810865
Dec 04, 2023
AUTOTESTE PARA ANTICORPO PARA DOENÇA CELÍACA
GLUTEN’ALARM® Homeuse
VEDALAB
81086830053
Jan 16, 2023
AUTOTESTE PARA ANTICORPO PARA DOENÇA CELÍACA
BIOSYNEX Autoteste Glúten
BIOSYNEX SA
80686360311
Feb 25, 2021

