HYGISUN Covid-19 rapid test for laypeople
The HYGISUN COVID-19 antigen rapid test (colloidal gold) is an antigen test approved by the BfArM in accordance with Section 11 (1) of the Medical Devices Act (MPG) for self-use by laypeople. The file number of the special approval is: 5640-S-058/21.
The lay test manages completely without the nose and / or throat swab, which is usually perceived as very uncomfortable.
The HYGISUN COVID-19 antigen rapid test (colloidal gold) relies on the new test method in which the sample is simply taken from a saliva discharge, known colloquially as the “spit test”. This release of saliva enables a qualitative in vitro determination of the novel coronavirus antigen.