Antigen rapid test kit - Import export

The SARSCoV2 Antigen Rapid Test Kit is a colloidal gold enhanced double antibody san dwich immunoassay for the qualitative determination of SARSCoV2 antigen.The test region (T) of nitrocellulose membrane was immobilized with mouse anti SARSCoV2 antibody 1 (Ab1), and the control region (C) was immobilized with Goat anti chicken IgY antibody (GAC). At the same time, the binding pad of the test card was fixed with mouse anti SARSCoV2 antibody 2 (Ab2) a nd chicken IgY (CIgY) which were both labeled by colloidal gold.

This SARS-CoV-2 & Flu A+B Antigen Combo Rapid Test Kit is only used for rapid in vitroqualitative detection of SARS-CoV-2, influenza A and influenza B nucleoprotcin antigens innasopharyngeal swab, nasal swab, oropharyngeal swab or saliva specimens. It is intended toaid in the rapid differential diagnosis of SARS-CoV-2, influenza A and influenza B viral infections. Negative test results do not preclude SARS-CoV-2 or influenza infections andshould not be used as the sole basis for treatment or other patient management decisions.

With the self/rapid test you get a high-quality corona antigen self-test, which is used for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in the front nasal cavity in a short time. It is based on the lateral flow immunoassay method, which uses antibodies to detect specific antigens in the sample swab.

Easy handling thanks to minimally invasive sampling as a nasal swab (2.5 cm depth) Also very good for use with small children, students, handicapped people, professional sports activities and in companies This test is Made in Germany and approved for use by laypersons Reliable with 100% sensitivity and 98% specificity

BfArM listed: AT563/21 Evaluated by the Paul Ehrlich Institute Reliable with 96% sensitivity and 99% specificity Use only by medically trained personnel

Rapid antigen test COVID-19 swab test LIFECOSM - 25 pieces - SARS-CoV-2 to the extended 4in1 successor article most sensitive rapid corona test in Germany according to the Paul Ehrlich Institute (PEI) listed at the BfArM 100% overall sensitivity according to PEI -> AT1054/21 | AT 1055/21 | AT1056/21 | AT1340/21 | AT1361/21 -> same test cassette detects current virus mutations, reliable at Omikron reimbursable by test regulation