Rapid Antigen Test Kit SARS-CoV-2 Antigen Rapid Test Professional Diagnostic Use High Accuracy CE Certificated
Intend Use
The SARS-CoV-2 Antigen Rapid Test Kit is used for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP), oropharyngeal (OP) and nasl swab specimen.
Product Details
Item | Value |
Model Number | LX-401301 |
Package | 20 Tests/Kit |
Warranty | 24 Months |
Quality Certification | CE |
Safty Standard | ISO13485 |
Sample Volum | 3 Drops |
Sample Type | Nasopharyngeal ( NP), oropharyngeal ( OP) and nasal swab specimen |
Test Speed | Within 15 minutes |
Main Components
Analytical Results
Product Features
Use Steps
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 colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).
Negative: Only one colored band appears, in the control region (C). No apparent colored band appears in the test region (T).
Invalid: If there is no Control line (C) or only a Test line (T) in the result window, the test did not run correctly and the results are not valid.
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 |
Precautions
1. For IN VITRO diagnostic use only.
2. Reagents should be used as soon as possible after opened. This reagent cannot be reused for disposable.
3. 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.
4. All specimens and reagents should be considered potentially hazardous and handled in the same manner as an infectious agent after use.
Application
Certificate