Product Details
SARS-CoV-2 Antigen Rapid Test Kit Professional Test Use 20Tests /
Kit CE Certificated Simple Operation Rapid Test Kit
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 |
Type | 20 Tests/Kit |
Specificity | 100% |
Sensitivity | 98.04% |
Accuracy | 99.60% |
Warranty | 24 Months |
Quality Certification | CE,MSDS |
Safty Standard | ISO13485 |
Sample Volum | 3 Drops |
Main Components
- Test Cassettes
- Sample tubes with Prefilled Sample extraction buffer
- Swabs
- Tube Stand
- Instruction for use
Analytical Results
SARS-CoV-2 Antgen Rapid Test Kit |
Sensitivity | Specificity | Total Accuracy |
98.04% | 100.00% | 99.60% |
Product Features
- Quick test, get the result within 15 minutes
- Reliable, high accuracy, sensitivity and specificity
- Easy for use, one step operation process
- Best quality, CE certificated
Use Step
- Take a sample tube (with prefilled sample extraction
solution).Remove the aluminum foil sealing of the prefilled sample
extraction tube and then put the tube into the tube stand.
- Dip the swab into the sample extraction liquid after sample
collection, fully immerse the tip of the swab, rotate and squeeze
the swab 10 times, then pull out the swab, and take the stranded
liquid as much as possible.
- 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.
Read the result 15-20 minutes after adding the sample. Result got
after 20 minutes is invalid.
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
- For IN VITRO diagnostic use only.
- Reagents should be used as soon as possible after opened. This
reagent cannot be reused for disposable.
- 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.
- All specimens and reagents should be considered potentially
hazardous and handled in the same manner as an infectious agent
after use.
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.