Product Details
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
Company Profile
Labnovation Technologies, Inc. is an original manufacturer
established in Shenzhen, China since 2001. We are dedicated in
developing and manufacturing IVD instruments and reagents including
HbA1c analyzer and reagents, rapid test reader & reagents,
hematology reagents, clinical chemistry reagents, electrolyte
reagents, wash solution and urine test reagents.
Labnovation products are developed in house, tested extensively in
clinics and passed strict quality controls. All of our products are
CE marked and approved by SFDA. In the past 15 years, our products
have been exported to 110 different countries and used in 8000
hospitals worldwide. We provide both ready-to-use final products
and bulk OEM reagents, including ready-to-use reagents,
concentrated, and powder.
With an investment of 10% of our annual sales into R&D, we
release new products every years. We win more and more domestic and international cooperation by
company reputation and products quality while we actively take part
in fairs like MEDICA,AACC, ARBA HEALTH and so on through which we
are well-known by the companies in this field.