Rapid Test Kit Antigen Saliva Rapid Diagnostic Test High Accuracy
Virus Antigen Rapid Test Kit Self Test Use
Intend Use
- This rapid test kit is intended for the qualitative detection
of SARS-CoV-2 antigen in human saliva samples from novel
coronavirus suspected person with symptoms within 7 days from
onset.
- The antigen saliva rapid test kit is an immunochromatography
assay.
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 |
Product Feature
- High specificity and sensitivity
- Immunochromatography method
- Non-invasive sample
- One step operation
- Quick testing, get the result in 15 minutes
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 |
Applications
- Center for diseasecontrol and prevention
- Primary health care institution
- Industrial production enterprise
- Detention center
- Public institution