Corona antigen self-test (front nose), set of 1
Corona antigen self-test (front nose), set of 1
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Product description
Corona antigen self-test (front nose)
Omicron Certified
This COVID-19-N antigen rapid test is used for the qualitative detection of antigens (N protein) of SARS-CoV-2 via a swab in the anterior nasal area (approx. 1.5-2cm).
The rapid test is approved by the Federal Institute for Drugs and Medical Devices (BfArM).
COVID-19 is a contagious and acute infectious disease of the respiratory tract. According to current epidemiological studies, the incubation period is 1 to 14 days, usually 3 to 7 days.
The main symptoms include fever, fatigue and dry cough. In some cases, nasal congestion, runny nose, muscle and throat pain also occur.
This test is suitable for laypeople of all ages. Children and adolescents under 18 years of age should be assisted by an adult.
The test is easy to use, fast and reliable.
The accuracy of the test for detecting COVID-19 disease in infected people is 100% and the detection of healthy people is 98%.
It is easy to use. Everything you need for the test is included in the package. To carry out the test safely and reliably, follow the instructions.
You can read the result within 15-20 minutes.
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package contents
- Test cassette
- Sample extraction buffer
- Swab
- Disposal bag
- Test instructions
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Test instructions:
- Take the swab out of the packaging and carefully insert it, cotton swab first, into one nostril to a depth of about 2 cm. Now move the swab along the nasal wall in a circular motion for 15 seconds.
- Open the sampling tube at the large opening and insert the swab with the collected sample into the tube.
- The sample must be soaked in the sample extraction buffer liquid (at least 15 seconds).
- Pack the swab in the enclosed plastic bag.
- Open the test cassette.
- Open the sampling tube at the small front screw connection and add 4 drops of the treated sample into the sample hole S of the cassette.
- After 15 minutes you can read the result.
Paul Ehrlich Institute comparative evaluation of sensitivity