Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

ANTIBODY FOR CELIAC DISEASE - ANVISA Registration 80113770055

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 80113770055 and manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD.. The registration is held by ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPP 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80113770055
Registration Details
ANVISA Registration Number: 80113770055
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Família Autoteste Glúten
Risk Class II

Registration Details

80113770055

25351147194202513

03098281000155

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01