EDELVITAL™ is pleased to announce its new 3in1 Rapid COVID-19 Antigen test for the detection of SARS-CoV-2 in adults and children. The EDELVITAL™ 3in1 Rapid Test is registered for both professional and layman use in Austria, and is specially designed for ease of use. It can be used as “lollipop” test for children by placing the swab on the tongue after coughing and allowing it to absorb saliva (saliva test). The swab can also be placed in the first 2.5cm of the anterior part of the nasal passage (nasal test), or the throat (oropharyngeal test). If necessary it can also be used anally (anal test) during hospitalisation.

The antigen test also detects antigens of the SARS-CoV-2 Omikron variant (B.1.1.529), the Delta variant (B.1617.2), the Beta variant 501.V2 (N501Y.V2 or B.1.351) and the Alpha variant of the corona virus VOC-202012/01 (also 20I / 501Y .V1 or B.1.1.7 or B117).

Ideal for children &
the elderly.

The EDELVITAL™ 3 in 1 Rapid COVID-19 Antigen test is one of the mostly highly accurate on the market. As approved by the Paul Ehrlich Institute in Germany, and registered with the German Medical regulator BfArM, with a specificity of 100%. The less invasive test for children and the elderly can be used by placing the swab on the tongue after coughing and allowing it to absorb oral saliva, sometimes referred to as the “Lollipop test”.

Antigen Tests

3in1 Rapid COVID-19 Antigen Test Kit (Colloidal Gold)





3in1 Rapid COVID-19 Antigen Test (Colloidal Gold)





EDELVITAL™ 3in1 Rapid COVID-19 Antigen Test kit

3 in 1 specimen collection

Saliva swab
Saliva swabtest
Less invasive – ideal for children and the elderly.
Anterio nasal swab
Anterio nasal swabtest
Position the swab 2.5 cm into the nasal chamber.
An Oropharngeal
An Oropharngealtest
Position the swab at the back of the throat.

CE, EU IVD certified &
BfArM & GÖG listed

CE – IVD Certification 
EDELVITAL ™ COVID-19 tests are CE certified
according to 98/79 guidelines for medical in vitro diagnostics, appendix III, and
are listed at BfArM Germany & GÖG Austria.

Applicable standards:
ISO 13485: 2016, ISO 14971: 2019, EN ISO 18113-1: 2011, EN ISO 18113-2: 2011,
EN ISO 18113-3: 2011, EN 13641: 2002, ISO 15223-1: 2016,
EN 13612: 2002, ISO 23640: 2015, EN 62366-1: 2015

Air Queen Masken - CE, FDA, Halal zertifizierte FFP2 Atemschutzmasken

Rapid COVID-19 Antigen 3 in 1 Test
Unique features

The unique features of this test in comparison to other Antigen tests on the market is five-fold.

  • Firstly, the test uses a unique collection vial that completely eradicates the need for having to work with a separate buffer solution. This means no mistakes in dosage or spillage of the contents, maintaining the integrity of the test, saving costs on tests lost to human error.

  • Secondly, as a direct result of the solution integrated test tube, the test is much faster than other antigen test presently on the market.

  • Thirdly, this test has been produced as a result of extensive research into the efficiacy of the integral components, allowing a larger category of sample sites from which to quickly retrieve a test sample, within or without a hospital setting.

  • Fourthly, the product is very stable at room temperature and can be stored for 24 months at 2-30 degrees centigrade.

  • Fifth, the product is easy to ship and store and does not rquire refridgeration.

Certifications, validations, listings

  • CE certified

  • IVDD 98/79 / EC

  • BfArM Germany listing

  • GÖG Austria listing

  • Validated by the Paul Ehrlich Institute

  • ISO 13485 certified manufacturing

  • Austrian PCN entries


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