High Accuracy SARS-CoV-2 Antigen Rapid Test Kit RTK Antigen Test Kit Approved By KKM
Rapid Test Kit SARS-CoV-2 Antigen Rapid Test Kit High Accuracy Professional Testing Kit
Product Details
| Item | Value |
| Model Number | LX-401301 |
| Type | 20 Tests |
| Warranty | 24 Months |
| Sensitivity | 98.04% |
| Specificity | 100% |
| Power Source | Instruction Manual |
| Quality Certification | CE |
| Safty Standard | ISO13485 |
| After-sale Service | Online technical support |
| Sample Type | Nasopharyngeal swab or Oropharyngeal swab |
| Sample volume | 3 Full drops |
| Test Speed | Within 15 minutes |
Product Feature
- Detection od mutations
- Safety and Reliability
- Simple Operation
- Esay to read the result
Intend Use
- This rapid test kit is intended for the qualitative detedtion of SARS-CoV-2 infection from patients.
- Results from this test kit should not be used as the sole basis for diagnosis.
- The test provides preliminary test results.
- Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for treatment or other management decision.
Main Components
- 20 Test Cassettes
- 20 Sample tubes
- 2 Sample extraction Buffers
- 20 Swabs
- 1 Instruction for use
Use Step
Notic: When using viral transport medium (VTM), it is important to ensure that the VTM containing the sample is warmed to room temperature. Cold samples will not flow correctly and can lead to erroneous or invalid results. Several minutes will be required to bring a cold sample to room temperature.
- 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. | Others |
Certificate
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