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ANTIBODY FOR CELIAC DISEASE - ANVISA Registration 80105220280

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 80105220280 and manufactured by AESKU DIAGNOSTICS GMBH & CO. KG. The registration is held by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS 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.

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80105220280
Registration Details
ANVISA Registration Number: 80105220280
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Device Details

AESKUCARE® Gluten Related Disorders IgA
Risk Class II

Registration Details

80105220280

25351088661202566

04299232000143

Company Information

Dates and Status

Jul 07, 2025

VIGENTE

09/18/2025 19:00:01