Saliva Rapid Test

Are you tired of pushing a swab down your throat until you are in tears?
Then is our saliva rapid test made for you.
Our Saliva Rapid Test is CE-IVD approved and tested for self-testing.
This test is so simple that anyone can do it by themselves.

The Saliva COVID-19 Antigen Detection Kit (Colloidal Gold) is a non-invasive test in which saliva is collected in a collection tube with extraction buffer. With this, two drops of the sample are applied to the test cassette via an on-site inspection method. After 10-15 minutes, this will indicate whether someone has antigens against COVID-19 in his or her saliva samples. The test does not have to be performed by a trained person. It can be used by everyone, including private use.



FEATURES

  • Non-invasive
  • Sensitivity 93,3% & specificity 99,5%
  • Easy to operate
  • No equipment required
  • CE-IVD approved

BENEFITS

  • SALIVA AS SAMPLE. The sampling of this kit makes it super easy and non-invasive. It also makes the test user-friendly. 
  • ON-SITE. With this kit, it is possible to take a corona test in any place. 
  • EASY. Everyone can take the test because of the simple design. 

Goffin Molecular Technologies is an authorized distributor of Lituo Biotechnology.

Just like Abbott, Roche, and Quidel, this test is registered in Europe and in possession of a valid CE certificate. This test also meets the minimum requirements of the Spanish RIVM. The Lituo saliva test has now also been officially approved for domestic use in the Czech Republic by the Ministry of Health. And more countries (including Austria) are busy validating this easy quick test. In the Netherlands, the exemption for use as a self-test for consumers has been applied. Due to the non-invasive sample collection, the rapid test is also ideal for use on children, the elderly, persons with disabilities.

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-certificaat. Ook voldoet deze test aan de minimum eisen van het Spaanse RIVM. De Lituo speekseltest is inmiddels ook in Tsjechië door het Ministerie van Volksgezondheid officieel goedgekeurd voor huishoudelijk gebruik. En meer landen (o.a Oostenrijk) zijn druk bezig met het valideren van deze gemakkelijke sneltest. In Nederland is de ontheffing voor gebruik als zelftest voor consumenten aangevraagd. Vanwege de niet-invasieve monsterafname is de sneltest ook ideaal voor gebruik bij kinderen, ouderen, personen met een handicap.


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

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