Nasopharyngeal Swab Rapid Influenza Diagnostic Test Kit For Infant Screening

Rapid Test Kit Antigen And Influenza A/B Rapid Test Kit Professional Use 20 Tests High Accuracy Rapid Test Kit

Intended Use

The rapid test kit is intended for qualitative detection and differentiation of nucleocapsid protein antigens from SARS-CoV-2, influenza type A and influenza type B in the same time directly from nasal/nasopharyngeal (NS/NP) swab, oropharyngeal (OP) swab and saliva specimens from patients with signs and symptoms of respiratory viral infection. The test kit is for professional use only.

Specification

Feature

• Convenience: On-site test that easily performed
• Fast: Result output within 15minutes
• High Aaccuracy, Sensitivity and Specificity

Application

• Clinical department, emergency department, fever department
• Disease control center, quick screening in epicenter
• Primary screening of influenza A/B virus
• Risk assessment of influenza A/B VIRUS
• High susceptible population and infant screening

Limitations

• This reagent is a qualitative detection reagent, which cannot determine the exact content of antigen.
• The test results of this reagent are only for the reference of clinicians and should not be taken as the sole basis for clinical diagnosis and treatment. Clinical management of patients should be considered in the light of their symptoms/signs, medical history, other laboratory tests and treatment responses.
• Restricted by antigen detection reagent method, the lowest detection limit (sensitivity analysis) is generally lower than that of nucleic acid detection, so the researchers deal with negative result to give more attention, should be combined with other test results comprehensive judgment, advice to doubt the negative result of nucleic acid detection or virus isolation culture identification method for review.
• False negative results may be caused by unreasonable sample collection, transport and treatment, and low viral load in samples.

Main Components

• Test cassettes
• Sample extraction buffers
• Sample tubes
• Swabs
• Tube Stand
• Instruction For Use

Use  Step

• Take out the test cassette from the sealed pouch, place it on a clean and level surface with the sample port well up.

• Apply 2 full drops of the treated sample (60μl-70μl) vertically into each of the two sample wells of the test cassette.

• Observe the test results immediately within 15~20 minutes, the result is invalid over 20 minutes.

Interpretation Of Result

• POSITIVE: The presence of T (T on nCoV /A or B on Flu) and C lines within the reaction window indicate a positive result on SARS-CoV-2 or Flu A and/or B infection or co-infection.

• NEGATIVE: One colored line appears in the control region(C). No apparent colored line appears in the test region (T on nCoV /A or B on Flu). The negative result does not indicate the absence of analytes in the sample, it only indicates the level of tested analytes in the sample is less than the minimum detection limit

• INVALID: No colored lines appear, or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.