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320 X NG Biotech COVID-19 (Home Self-Test) - CASE - (CE-IVD Certified)

€ 960.00

320 X NG Biotech Antigen Test (Case)  

DELIVERY TIME
Ireland - 24/48hrs via courier

NG Biotech COVID-19 (Home Self-Test) - 320X Single Test (Case) - CE-IVD Certified

Detects all variants including omicron

NG Biotech Rapid Antigen test (Home Self-Test) 

  • Antigen test (Home Self-Test) - tests for Covid-19 - results in 15 mins
  • 99.47% accuracy
  • This self-test is an EU Certified test for public/home use 
  • The Antigen Test comes in a convenient single unit box
  • Detects all Variants including omicron, Alpha , “Beta”, “Gamma”, “Delta”, “Epsilon”, “Mu”, “Lambda”, “Iota”, “Kappa”, “Eta”
  • Less invasive nasal swab - far more comfortable than other tests
  • The NG Biotech Antigen Test detects the nucleocapsid protein antigen from SARS-CoV-2 
  • The NG Biotech is a French biotech company developing and manufacturing novel in vitro diagnostic tools for Therapy Monitoring at Point-of-Care (onnsite).
  • The NG Biotech Ninonasal test is a home test and has an easy-to-follow ‘How-to’ video which can be accessed from the QR code on the box and on YouTube
  • Delivery time is 48 hours by courier
  • For larger volume orders (>1000) we can provide a larger discount – please contact customerservice@mybio.ie
  • After sales support for the test:

Email: customerservice@mybio.ie

Telephone: (056) 770 0868 

Documentation and Certification

EXCELLENT PERFORMANCE CHARACTERISTICS: 

  • Specificity:  98% 
  • Sensitivity:  99% 
  • Accuracy:    >99% 

This product is CE-IVD marked for professional use and complies with the European In-Vitro Diagnostic Devices Directive (98/79/EC) for home use. 

(Note: QR code on side of box to ensure user can complete the test correctly)

About this home test

Rapid SARS-CoV-2 Antigen Test Card is an immunochromatography based one step in vitro test. It is designed for the rapid qualitative determination of SARS-CoV-2 virus antigen in anterior nasal swabs from individuals suspected of COVID-19 within the first seven days of symptom onset. Rapid SARS-CoV-2 Antigen Test Card shall not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection. Children under 14 years of age should be assisted by an adult. 




NG Biotech is a family company, based in France that specialise in rapid, mobile, and connected bioassays. The company designs and manufactures innovative solutions to meet different needs: response to medical emergency, needs in laboratories, and near-patient needs. Since its creation in 2012, in just a few years, NG Biotech has managed to establish itself as a company of choice in various areas, especially in the bacteriology field with rapid detection of antibiotic-resistant bacteria, as well as in the field of women’s health with pregnancy tests from one drop of blood. Those tests are available in more than 50 countries across the world and are widely used in the EU and the United States.

Established in Brittany (France), NG Biotech has a complete structure with a R&D laboratory, and two production facilities complying with international quality standards.
NG Biotech company positions itself above all to provide support and expertise to various major public health issues. 

Further information
The test kit is simple, safe, effective and intended for self-testing, which is suitable for individuals to use in non-laboratory settings like homes, offices, schools, sports stadiums, airports, etc.

Test Principle
During the test, the processed samples to be tested are added to the sample holes. When the sample contains SARS-CoV-2 antigen, it first combines with the colloidal gold-labelled anti-SARS-CoV-2 antibody. Chroma-tography is then performed. When it binds to the anti-SARS-CoV-2 monoclonal antibody previously immobilized on another membrane, a purple-red band will appear in the test area (T). If there is no SARS-CoV-2 antigen in the sample, there will be no purple-red band in the test area (T). A purple-red band will appear in the quality control area (C) regardless of the presence of new coronavirus antigen in the sample, which is used as a criterion to determine whether there is sufficient sample or the chromatography is processed properly. It is also used as an internal control standard for the test kit.


    This product is CE-IVD marked for professional use and complies with the European In-Vitro Diagnostic Devices Directive (98/79/EC) for home use.