Antigen Detection Test - Swabs

This rapid test makes use of nasopharynx swabs, oropharynx swabs, and nasal swabs.
Due to the simple test design, the test is easy to use. You just take a swab and 15 minutes later
you know if you have the coronavirus. Our rapid test is CE-IVD approved. 

The antigen detection test of NewGene makes use of nasopharynx swabs, oropharynx swabs and nasal swabs as a sample. This test is the only one that has different kinds of swabs for all three samples. The test is based on an immunochromatographic membrane assay that uses highly sensitive monoclonal antibodies to detect nucleocapsid protein from SARS-CoV-2. With just a few drops of sample and extraction buffer, you know in 15 minutes if you have corona or not. Our antigen detection test is CE-IVD approved for professional use. 



FEATURES

  • Easy to operate
  • Sensitivity 95,7 – 98,0%
  • Specificity 99,0 – 99,2%
  • No equipment required
  • CE-IVD approved

BENEFITS

  • ACCURATE. The double antigen method gives a high accuracy rate
  • ON-SITE. With this kit, it is possible to take a corona test in any place. 

Goffin Molecular Technologies is an authorized distributor of NewGene.

Just like Abbott, Roche, and Quidel, this test is registered in Europe and in possession of a valid CE and TüV certificate. This test also meets the minimum requirements of the RKI and PEI (the German RIVM) and is included in the BfArM list. The Federal Institute for Drugs and Medical Devices is an independent higher federal authority within the portfolio of the Federal Ministry of Health in Germany. The NewGene rapid test is registered in several countries including France, Italy, Portugal, Czech Republic, Belgium, Greece, Peru, and Argentina. And more countries (including Switzerland) are busy validating this easy quick test. CE certification for use as a consumer self-test has been requested.

Goffin Molecular Technologies is not liable for incorrect use, storage, results, and explanation of the rapid test and any resulting calamities.


Deze test is net zoals Abbott, Roche en Quidel geregistreerd in Europa en in bezit van een geldig CE en TüV certificaat. Ook voldoet deze test aan de minimum eisen van de RKI en PEI (het Duitse RIVM) en is opgenomen in de BfArM-lijst. Het Federaal Instituut voor Drugs en Medische Hulpmiddelen is een onafhankelijke hogere federale autoriteit binnen de portefeuille van het Federale Ministerie van Volksgezondheid in Duitsland. De NewGene sneltest is in meerdere landen geregistreerd waaronder: Frankrijk, Italië, Portugal, Tsjechië, België, Griekenland, Peru en Argentinië. En meer landen (o.a Zwitserland) zijn druk bezig met het valideren van deze gemakkelijke sneltest. Een CE-certificering voor gebruikt als zelftest voor consumenten is aangevraagd.

Goffin Molecular Technologies is niet aansprakelijk voor verkeerd gebruik, opslag, uitslag en uitleg van de sneltest en de eventueel daaruit voortvloeiende calamiteiten.

Fill in the form

and ask
us anything about our products

After completion, Goffin Molecular Technologies will contact you as soon as possible.

Skip to toolbar