HELICOBACTER PYLORI - ANVISA Registration 80048490045
Access comprehensive regulatory information for HELICOBACTER PYLORI in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80048490045 and manufactured by MONOBIND, INC. The registration is held by USA DIAGNOSTICA LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including VEDALAB, DIA.PRO DIAGNOSTIC BIOPROBES SRL, 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.

Janaina dos Santos de Miranda
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Registration Details
80048490045
25351016170201032
02330159000108
Company Information
Dates and Status
Apr 19, 2010
VIGENTE
09/18/2025 19:00:01
IMMUNOGLOBULIN G
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Celer Finecare H. pylori Teste Quantitativo
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IDK® Helicobacter pylori antigen ELISA
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81472060038
Feb 17, 2025