Realy Coronavirus (SARS-COV-2) Antigen Rapid Saliva Test Device 1 pc

A rapid test for the qualitative detection of antigens of the new Coronavirus with oral-pharyngeal smear.
The New Coronavirus Antigen Detection Rapid Test Cassette (SARS-Cov-2) is an in vitro diagnostic test for the qualitative detection of new coronavirus antigen in an oral-pharyngeal smear, using the rapid immunochromatography method. The detection is based on monoclonal antibodies specific for the new coronavirus antigens.
Provides information to clinicians for proper medication prescription.

Allow the test apparatus, sample and exhaust buffer to reach room temperature (15-30 ° C) before testing. 1. Remove the test device from the sealed aluminum package and use it as soon as possible. Place the test device on a clean, flat surface. Immediate testing after opening the package gives better and more accurate results. 2. Unscrew the sample collection tube cap. 3. Take a bottle of exhaust buffer, remove the cap and add all of the buffer into the exhaust tube. 4. Insert the sterile swab with the coating into the test extraction buffer. Rotate the swab for about 10 seconds while simultaneously pushing its head inside the tube to release the antigens from the swab. 5. Remove the sterile swab, while at the same time pressing its head inside the tube as you remove it, in order to extract as much liquid as possible from the swab. Dispose of the sterile swab according to the hazardous waste disposal protocol. 6. Place and tighten the cap on the sample collection tube, then shake the collected sample vigorously to mix the sample and the extraction buffer. See Figure 4. 7. Add 3 drops of solution (approx. 80ul) to the sample well and start the timer. Read the results in 10-20 minutes. Do not interpret the results after 20 minutes.

Interpretation of Results
POSITIVE: Two red lines appear. A red line appears in the control area (C) and a red line in the test area (T). The shade of color can vary, but in any case it should be considered positive, even if the line is faint.
NEGATIVE: Only one red line appears in the control area (C) and no line in the test area (T). Negative results indicate that there are no new coronavirus molecules in the sample or that the number of viral molecules is below the level of detection.
CANCEL: No red line appears in the control area (C). The test is invalid even if there is a line in the test area (T). Insufficient sample size or incorrect procedural techniques are the most likely reasons for line control failure.
Test the test procedure and repeat the test using a new test device. If the problem persists, stop using the test immediately and contact your local distributor.