Rapid Test Kit Antigen Rapid Test Kit SARS-CoV-2 Antigen Rapid Test Kit High Specificity Professional Test Kit
Intend Use
- Labnovation's SARS-CoV-2 Antigen Rapid Test Kit is intended for the qualitative detection of SARS-CoV-2 infection from patients.
- The test kit is an aid in the diagnosis of the patients with suspected SARS-CoV-2 infection in conjunction with clinical presentation and results of other laboratory tests.
- To be attention the test kit is provides preliminary test results and should not be used as the sole basis for treatment or other management decision.
Product Details
Item | Value |
Model Number | LX-401301 |
Packaging | 20 Tests/Kit |
Warranty | 24 Months |
Quality Certification | CE, MSDS |
Safty Standard | ISO13485,ISO9001 |
Specimen | nasopharyngeal swabs and oropharyngeal swabs |
Sample volume | 3 Full drops |
Test Speed | Within 15 minutes |
Sensitivity | 98.04% |
Specificity | 100% |
Total coincidence rate | 99.6% |
Product Feature
- Fast
- Easy to use
- Room temperature storage
- Qualitative
- Professional


PRINCIPLE
This kit is an immunochromatography assay. According to the gold immunochromatographic test principle, double antibody sandwich method was used to detect SARS-CoV-2 nucleocapsid antigen in the samples. Whether the sample contains antigen or not, the gold monoclonal antibody will bind to the enveloped antibody at the quality control line, form a compound and condense into a red band.

Main Components
- 20 Test Cassettes
- 20 Sample tubes
- 2 Sample extraction buffer
- 20 Swabs
- 1 Instruction for use
Use Step
- Add 550μL sample extraction (about 22-24 drops) into the sample tube.
- Insert the swab into the sample tube prefilled with extraction buffer. Mix well and squeeze the swab 10-15 times by compressing the wall s of the tube against the swab.
- Roll the swab head against the inner wall of the tubes as you remove it. Try to release as much liquid as possibe. Dispose of the used swab in accordance with your biohazard waste disposal protocol.
- Close the cap of the sample tube.
- Add 3 full drops of the mixed solution vertically into the sample well (S) of the test cassette.

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. | Other |
Other Information
- For IN VITRO diagnostic use only.
- Reagents should be used as soon as possible after opened. This reagent cannot be reused for disposable.
- The test device should remain in the sealed pouches until use. If sealing problem happens, do not test. Don’t use after the expiration date.
- This reagent is a qualitative detection reagent, which cannot determine the exact content of antigen.
- The test results of this reagent are only for the reference of clinicians and should not be taken as the sole basis for clinical diagnosis and treatment. Clinical management of patients should be considered in the light of their symptoms/signs, medical history, other laboratory tests and treatment responses.
Certificate
