This kit is intended for the in vitro qualitative detection of antigens of 2019-nCoV,
Influenza A virus (IAV) or Influenza B virus (IBV) in human nasopharyngeal swabs or
oropharyngeal swabs specimens.
This kit cannot be used to differentiate different virus subtypes. It is suitable for the
auxiliary diagnosis of respiratory tract infection caused by targeted viruses; the results
are for clinical reference only and cannot be used as the sole basis for diagnosis and
exclusion decision. Clinical diagnosis and treatment of patients should be considered in
combination with their symptoms/signs, medical history, other laboratory tests and
treatment responses.
Positive test result needs to be further confirmed. Negative result does not preclude the
possibility of infection.
This kit is intended for use by qualified and trained clinical laboratory personnels
specifically trained in the techniques of in vitro diagnostic procedures.
