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
Safty Standard	ISO13485
Sample Type	Saliva Sample
Sample volume	3 Full drops
Sensitivity	Over 95%
Specificity	Over 95%
Total Accuracy	Over 95%

Product Feature

Diagnostic Accuracy

SARS-CoV-2 Antigen Saliva Rapid Test Kit
Sensitivity	Specificity	Total ACCURACY
96.19%	100.00%	99.21%

Main Components

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