SARS-CoV-2 Rapid Antigen SALIVA

SARS-CoV-2 Rapid Antigen SALIVA

Detects the virus antigen in saliva samples. The kit is intended for self-testing at home, as well as testing in a clinical and diagnostic laboratory by qualified specialists. For in-vitro diagnostics.

SARS-CoV-2 Rapid Antigen SALIVA

Produced by

The Republic of Korea

Country of origin

The Republic of Korea

Antigen

Detects

Antigen

Saliva

Biomaterial

Saliva

SARS-CoV-2 Rapid Antigen SALIVA

100%

Specificity

100%

Sensitivity

hourglass

20 minutes - ready time

thermometer

Easy to use, no laboratory equipment required

thermometer

Helps in confirming the diagnosis

Product overview

1 / 3

The first test kit on the market for home use. Detects the SARS-CoV-2 antigen in a human saliva sample. This test detects the SARS-CoV-2 antigen in human biological material (saliva) by the immunochromatographic method. The kit is intended for self-testing at home, as well as testing in a clinical and diagnostic laboratory by qualified specialists. For in-vitro diagnostics. For one-time use only

three cubes Kit contains:

The kit contains:

  • Test cassette - 1 pc.
  • A test tube with a buffer for extracting a biological sample - 1 pc.
  • A tube filter cap - 1 pc.
  • Funnel for collecting saliva - 1 pc.
  • Instructions for use - 1 pc.

Use order

Biomaterial sampling

Biomaterial sampling

Adding 10 μL of sample to the well

Adding 10 μL of sample to the well

Expect the result according to the time in the instructions

Expect the result according to the time in the instructions

Interpreting the rapid test results

result

If the (C) line turns red:

The test returned a negative result for the presence of coronavirus antigen.

result

If the (C) line turns red and the (T) line turns black:

The test returned a positive result for the presence of coronavirus antigen.

result

If the (C) line in the window does not turn red:

The test result is invalid. Possible causes could include non-compliance with biological sample collection requirements, and/or analysis procedures, or the test system used is faulty.