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EMA Product

Helicobacter Test INFAI

Product approved by European Medicines Agency (EU)

Basic Information

Helicobacter Test INFAI

Regulatory Information

EMEA/H/C/000140

Authorised

August 14, 1997

April 16, 1997

21

August 20, 2024

Company Information

Germany

An der Kohlenbahn 39 D-58135 Hagen

INFAI, Institut für biomedizinische Analytik & NMR-Imaging GmbH

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Helicobacter Test INFAI may be used for in vivo diagnosis of gastroduodenal Helicobacter pylori infection in: - adults; - adolescents, who are likely to have peptic ulcer disease. Helicobacter Test INFAI for children aged three to 11 years may be used for in vivo diagnosis of gastrduodenal Helicobacter pylori infection: - for the evaluation of the success of eradication treatment, or; - when invasive tests cannot be performed, or; - when there are discordant results arising from invasive tests. This medicinal product is for diagnostic use only.

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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