HELICOBACTER PYLORI - ANVISA Registration 80721060021
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 80721060021 and manufactured by TURKLAB TIBBI MALZEMELER SAN. TIC. A.S.. The registration is held by JC Pharma & Health Comércio, Exportação e Importação 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, MONOBIND, INC, 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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Registration Details
80721060021
25351373341201474
01662176000171
Company Information
Dates and Status
Sep 01, 2014
VIGENTE
09/18/2025 19:00:01
HELICOBACTER PYLORI
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H. Pylori Rapid Test
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H.Pylori Antibody Test Kit
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82444370149
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GASTRO TEST
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Celer Finecare H. pylori Teste Quantitativo
GUANGZHOU WONDFO BIOTECH CO. LTD
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IDK® Helicobacter pylori antigen ELISA
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Apr 28, 2025
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Teste Rápido de Anticorpos H. pylori
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
81472060038
Feb 17, 2025