Product Details
Antigen Saliva Rapid Test Kit SARS-CoV-2 Antigen Saliva Rapid
Diagnostic Test Self Test Use Single Packing Easy 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.
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 |
Test Time | Within 15 minutes |
Product Feature
- Self-testing Use
- Without special equipment requirement
- Detect vireus directly and get result rapidly
- Room temperature storage
Diagnostic Accuracy
SARS-CoV-2 Antigen Saliva Rapid Test Kit |
Sensitivity | Specificity | Total ACCURACY |
96.19% | 100.00% | 99.21% |
Main Components
- Test Cassette
- Saliva Collector
- Disposable Pipettes
- Sample Extraction Buffer (single dose)
- Instruction Insert
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 |
Warning Information
- Keep out of the reach of children. Any child under age 16 shouldn’t
perform the test without parental guidance, or professional aid.
- Improper handling of specimen can lead to biological infections.
Avoid any direct contact with reagents or wastes.
FAQ
As we're manufacturer and our daily production capacity is 1000000,
so the shipping as soon as received payment.
We conducted a large number of clinical trials, the sensitivity and
specificity of above 95%, the overall accuracy of 99%, the accuracy
of the detection results is very high.
As we're manufacturer and our daily production capacity is 1000000,
we accept OEM/ODM.
Other information
- DISPOSAL The test kit can be disposed of with normal household
waste in accordance with applicable local regulations.
- A negative result does not rule out the infection of a SARS-CoV-2
infection. Therefore, the test should not be used as the only
reference for the clinical diagnosis. The result must be confirmed
by the PCR.
- After use, rinse hands or, in case of contact with the buffer
solution, the affected body parts thoroughly with water.
- If symptoms persist: Seek medical advice.
Company Profile
Labnovation Technologies, Inc. is an original manufacturer
established in Shenzhen, China since 2001. We are dedicated in
developing and manufacturing IVD instruments and reagents including
HbA1c analyzer and reagents, rapid test reader & reagents,
hematology reagents, clinical chemistry reagents, electrolyte
reagents, wash solution and urine test reagents.
Labnovation products are developed in house, tested extensively in
clinics and passed strict quality controls. All of our products are
CE marked and approved by SFDA. In the past 15 years, our products
have been exported to 110 different countries and used in 8000
hospitals worldwide. We provide both ready-to-use final products
and bulk OEM reagents, including ready-to-use reagents,
concentrated, and powder.
With an investment of 10% of our annual sales into R&D, we
release new products every years. We win more and more domestic and international cooperation by
company reputation and products quality while we actively take part
in fairs like MEDICA,AACC, ARBA HEALTH and so on through which we
are well-known by the companies in this field.