SARS-CoV-2 Antigen Saliva Rapid Test Kit Antigen Saliva Rapid Diagnostic Test Self Test Antigen Rapid Test Kit
Intend Use
The Labnovation SARS-CoV-2 antigen saliva rapid test kit is intended for the qualitative detection of SARS-CoV-2 infection.

Product Details
Item | Value |
Name | SARS-CoV-2 Antigen Saliva Rapid Test Kit |
Warranty | 24 Months |
Sample Type | Saliva Sample |
Sample volume | 3 Full drops |
Test Time | Within 15 minutes |
Store temperature | Store 2-30 ℃ |
Product Feature
- No pre-processing required, simple operation, do not need any extra instrument
- Rapid test, easy to interpert the result within 15 minutes.
- The effective supplement of antigen test window period.
- Transported and stored at room temperature

Diagnostic Accuracy
- Sensitivity: 96.19%
- Specificity: 100.00%
- Total Accuracy: 99.21%

Main Components
- Saliva Collector
- Disposable Pipettes
- Sample Extraction Buffer (single dose)
- Instruction Insert
- Test Cassette
Use Step
- Take sample tube with prefilled sample extraction buffer and remove the sealed film of the sample tube. Then put the tube into tube stand (in the outer box).
- Open the tear hole of the aluminum foil bag, take out the disposable pipette and test cassette, lay them flat.
- Put the saliva collection bag to lips and let the saliva flow into the bag.
Place the tip of tongue against the upper or lower tooth root to enrich saliva, and then swallow saliva to the throat without ingesting saliva to esophagus, followed by returning saliva to the mouth. Repeat the process for 5 times.

- Draw 2/3 dropper range(300ul)of saliva from saliva collection bag with the help of pipette and transfer the entire contents into the extraction buffer of the sample tube. And blow the liquid for 10 times, squeeze bottom of the sample tube to ensure the saliva is thoroughly mixed.
- Close the cap of the sample tube. Shake the specimen collection tube at least three times vigorously to mix the saliva sample with extraction buffer. Attention: Please avoid bubbles!
- Add 3 full drops of the treated sample extraction buffer (about 70μL-100μL) vertically into the sample well of the test cassette.
Read the result at 15 minutes. Do not interpret the result after 20 minutes.

Result Interpretation
-
POSITIVE: Two (2) distinct colored lines appear. One line should be in the control region (C) and the other line should be in the test region (T).
-
NEGATIVE: One (1) colored line appears in the control region(C). No apparent colored line appears in the test region (T).
-
INVALID: No colored lines appear, or control line fails to appear, indicating that the operator error or reagent failure.

Virus Sources
Global high frequency mutation | Alpha / B.1.1.7(U.K.) | Beta I B.1.351(South Africa) |
Gemma I P.1(Brazil) | Kappa I B.1.617.1(India) | Delta I B.1.617.2(India) |
C.37,ect | Alpha I B.1.17(U.K.) | B.1.36.16.etc |
A.2.5,etc | A.23.1 | Alpha I B.1.17(U.K.) |
B.1.1.33.etc | C.1.1.etc. | Omicron |
Application
- People with symtoms in the early stage
- Regular screening
- Hospital / Clinic
- Office
- High-risk congregate
- School
Other Infromation
- This kit is a qualitative detection, which cannot determine the exact content of antigen.
- Do not use the test if the packaging is damaged. Do not use broken test components.
- All test components are only intended to be used for this test. Do not reuse the test or test components.
- The test should be carried out immediately or within one hour after opening the foil pouch (18-30°C, humidity <60%).