HELICOBACTER PYLORI - ANVISA Registration 80002670069
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 80002670069 and manufactured by RENYLAB QUÍMICA E FARMACÊUTICA LTDA. The registration is held by RENYLAB QUÍMICA E FARMACÊUTICA 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Registration Details
80002670069
25351674829201099
00562583000144
Company Information
Dates and Status
Dec 20, 2010
VIGENTE
09/18/2025 19:00:01
HELICOBACTER PYLORI
UREASE
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10443010012
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FAST TEST H. PYLORI
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Jun 04, 2018
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Biohit Helicobacter pylori UFT 300
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10300390628
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H. Pylori Rapid Test
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80638720095
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GASTRO TEST
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82146060003
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Celer Finecare H. pylori Teste Quantitativo
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80537410145
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IDK® Helicobacter pylori antigen ELISA
IMMUNDIAGNOSTIK AG
80464810928
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RIDASCREEN® Helicobacter
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82890930009
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Teste Rápido de Anticorpos H. pylori
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
81472060038
Feb 17, 2025