Testing Kit Infectious Disease Diagnostic Kit Rapid Test Device SARS-CoV-2 &Influenza A + B Antigen Rapid Test Kits

Testing Kit Infectious Disease Diagnostic Kit Rapid Test Device SARS-CoV-2 &Influenza A + B Antigen Rapid Test Kits

----------------------------------------- Product Description ---------------------------------

      The Test Kit is an in vitrodiagnostic test for determining the presence of SARs-CoV-2, influenzaA (fu A) and/or influenza B fu B) antigens in antericna5al5Wa 0nples.This test isintended for self-collected anterior nasal swafromindividuals over 14 years old or adult collected anterior nasal swalfromindividuals aged 2 years orolderwithsymptoms of respiratory infectiorswithin the first 6 days ofsymptom onset.

      The kit is capable of simultaneously detecting three viral antigens in human pharyngeal or nasal swab samples, providing clinicians and patients with a timely and reliable diagnostic basis.

----------------------------------------- specificities ---------------------------------

------------------------------------- Product Components -----------------------------

●Test card: used to carry the sample and perform antigen-antibody reaction.
●Sample Buffer: Used to dilute and process the sample to increase the sensitivity of the test.
●Swab: Used to collect pharyngeal or nasal swab samples from the subject.
●Instruction manual: Detailed instructions on how to collect samples, perform the test and read the results.

----------------------------------------- Methods of use ---------------------------------

●Sample Collection: A swab is used to collect separate pharyngeal and nasal swab samples from the subject, ensuring that sufficient mucus and cells are collected.
●Sample processing: Place the swab sample into the sample tube, add buffer and rotate the swab.
●Test operation: Drop the processed sample into the sample well of the test card and start the timer.
●Result Interpretation: Observe the color change on the test card within the specified time according to the instructions to determine whether the sample contains SARS-CoV-2, Influenza A or Influenza B antigen.