© 2020.Spartacus-Biomed
This test is CE marked (98/79/CE) and has been recently successfully tested by Pasteur Institute Paris (French National Reference Center for Covid-19 tests) with a specificity of 100 % for both IgG and IgM and a sensitivity of 96 % and 92%, respectively.
Spartacus-Biomed registered this test to the ANSM (Agence Nationale de Sécurité du Médicament et des produits de santé: National Agency for the Safety of Medicines and Health Products). Therefore, the LFA COVID-19 IgG & IgM Rapid Test Device is approved by the French Ministry of Health and is reimbursed by Social Security.