This kit is only used for the in vitro qualitative detection of Multiple Respiratory Multipathogen Antigen(SARS-CoV-2/Respiratory Syncytial virus/Influenza A virus/Influenza B virus/Adenoviruses/M.pneumoniae)from human nasopharyngeal swabs specimens.SARS-CoV-2/RSV/ADV/MP&Flu A/B Antigen Rapid TestKit is an immunochromatographic double-antibody sandwich assay intended for the qualitative detectionand differentiation of SARS-CoV-2/Respiratory Syncytial virus/Influenza A virus/Influenza B virus/Adenoviruses/ M.pneumoniae from individuals who are suspected of respiratory tract disease infection.This kit is suitablefor the auxiliary diagnosis of respiratory diseases the results are for clinical reference only and cannot beused as the sole basis for diagnosis and exclusion decision. The clinical diagnosis and treatment of patientsshould be considered in combination with their symptoms/signs medical historyother laboratory tests andtreatment responses, Positive test result needs to be further confirmed negative result does not precluderespiratory diseases viruses infection.

The kit is immunochromatographic and uses double-antibody sandwich method to detect SARS-CoV-2/ Respiratory Syncytial virus/Influenza A virus/Influenza B virus/Adenoviruses/M.pneumoniae. During detection,the treated specimens are loaded into the sample wells of the test card.When the concentration ofSARS-CoV-2/Respiratory Syncytial virus/Influenza A virus/Influenza B virus/Adenoviruses/M.pneumoniae in specimen is higher than the minimum detection limit. the viral antigen will form complexes with labeledantibodies first. Under chromatography, the complexes move forward along the nitrocellulose membrane tillcaptured by pre-coated monoclonal antibody of SARS-CoV-2/Respiratory Syncytial virus/Influenza A virus/ Influenza B virus/Adenoviruses/M.pneumoniae in detection zone on nitrocellulose film(T1/T2/A/B) to form a redreaction line on the detection zone at this point the result is positive. Conversely, if there is no viral antigen or theconcentration of antigen in specimen is below the minimum detection limit, no red reaction line appears inthe detection zone, at this point the result is negative.Regardless of whether the sample contains viralantigens or not, a red reaction line will appear in the quality control zone(C),the red reaction line that appearsin the quality control zone(C) is the criterion for determining if the chromatography process is normal.