High Sensitivity SARS-CoV-2 Antigen Rapid Test Kit 99% Accuracy Professionla Use
Rapid Test Kit SARS-CoV-2 Antigen Rapid Test Kit High Quality High Sensitivity Antigen Rapid Test Kit
Intend Use
- SARS-CoV-2 antigen rapid test kit is intended for the qualitative detection of SARS-CoV-2 infection from patients. It is for professional use only. It 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. .
- It provides preliminary test results. To be notic, the negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for treatment or other management decision.
Product Details
| Item | Value |
| Product Name | SARS-CoV-2 Antigen Rapid Test Kit |
| Model Number | LX-401301 |
| Type | 20 Tests/Kit |
| Sensitivity | 98.04%, |
| Specificity | 100% |
| Total Accurracy | Over 99% |
| Warranty | 24 Months |
| Quality Certification | CE |
| Safty Standard | ISO13485,MSDS |
| Sample Type | Nasal, Oropharynx Swab |
| Sample volume | 3 Full drops |
| Test Speed | Within 15 minutes |
| Humidity | ≤60% |
| Gurop | Universal |
Product Feature
- Fast recation, the testing speed is very quick, read the result within 10-15 mins
- High accuracy, the total accuracy is over 99%
- High quality, can detection mutationvirus
- Safety, no extra requirement
- Simple to operate, fasy for use
Main Components
- 20 Test Cassettes
- 20 Sample tubes
- 2 Sample extraction buffers
- 20 Swabs
- 1 Instruction Manual
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.
Note
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.
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. | etc. |
Certificate
FAQ
- MOQ is ?
We have the MOQ limit, which is 10000 pieces.
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Business to business account.
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