Our Products


Probe4Pylori®  is the first kit of Biomode to obtain CE marking. The kit is intended to use in gastric biopsies for the rapid identification of clarithromycin resistance in H. pylori strains.

Food Safety

The first kit from Biomode to enter the market – Probe4Cronobacter® – will allow the detection of Cronobacter spp. in Powdered Infant Formula (PIF) soon to be followed by two other kits for the detection of Salmonella spp. and Listeria monocytogenes.


Several products under development:

  • Probe4Campylobacter
  • Probe4Vibrio
  • Probe4Ec0157



We can offer subcontracting services under the quality control system of ISO 9001:2008 and ISO 13485:2013 for medical devices.

Custom-made probes

Biomode offers a service of custom-made probes to target pathogens that you desire to identify. As an example, we already developed kits for Staphylococcus epidermidis and for  S. aureus. Talk with us about your research needs.

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Who we are

Biomode S.A. is an innovative Portuguese company in the biotechnology field that develops and commercializes rapid diagnostic kits for the identification and detection of foodborne and clinical pathogens. Our kits will respond to the need for food safety industry and clinical analysis to have more rapid, accurate and economic testing.

How we do it

We develop our kits based on Peptide Nucleic Acid FISH (PNA-FISH) technology for a rapid and accurate pathogen detection.
Unlike other molecular methods, PNA-FISH does not involve DNA extraction or amplification, is not susceptible to inhibitory compounds and only detects viable bacterial cells.


Latest news

Probe4Cronobacter is in the final stage of the PTM validation process from AOAC. Biomode is intensifying its efforts in the development of new products to increase its food safety related portfolio: 2 news products are in the final stage of development

CE marking of Conformity Our In vitro Medical Device: Probe4Pylori® just obtained the CE marking of Conformity

Biomode is now a Certified Company using a Quality Management System According to ISO 9001:2008 and to UNE-EN ISO 13485:2013 for Medical Devices.