Rapid Antigen Test Kit SARS-CoV-2 Antigen Rapid Test Kit Simple Operate Professional Testing Rapid Test Kit
Intend Use
 This rapid test kit is intended for the qualitative detection of SARS-CoV-2 infection from patients. 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. Results from this test kit should not be used as the sole basis for diagnosis. The test provides preliminary test results and should not be used as the sole basis for treatment or other management decision. Professional use only.
Product Details
| Item | Value | 
| Model Number | LX-401301 | 
| Type | 20 Tests/Box | 
| Sensitivity | 98.04%, | 
| Specificity | 100% | 
| Warranty | 24 Months | 
| Power Source | Instruction Manual | 
| Quality Certification | CE | 
| Safty Standard | ISO13485,MSDS | 
| Sample volume | 3 Full drops | 
| Test Speed | Within 15 minutes | 
 
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
Product Feature

  
  
  
 Main Components

  Sample Collection
 Use Step

  
 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. | 
 
 Certificate
 