Product Details
Rapid Antigen Test Kit SARS-CoV-2 Antigen Rapid Diagnostic Test
Professional Testing CE Certificated 20Tests/Kit
Intend Use
The Labnovation SARS-CoV-2 antigen rapid test kit is intended for
the qualitative detection od SARS-COV-2 infection from patients. It
is used for in vitro qualitative detection of the antigen of novel
virus in human nasopharyngeal or Oropharyngeal swabs.
Product Details
Item | Value |
Model Number | LX-401301 |
Type | 20 Tests/Kit |
Warranty | 24 Months |
Quality Certification | CE |
Safty Standard | ISO13485 |
Sample Type | Nasopharyngeal / Oropharyngeal Swab |
Sample Volume | 3 Full drops |
Main Components
- Test Cassettes
- Sample tubes with Prefilled Sample extraction buffer
- Swabs
- Tube Stand
- Instruction for use
Analytical Results
SARS-CoV-2 Antigen Rapid Test Kit |
Sensitivity | Specificity | Total Accuracy |
98.04% | 100.00% | 99.60% |
Product Features
- High effective, Low cost
- One step operation, without extra equipment
- Rapid testing, get the result within 15 minutes
- High accuracy, sensitivity and specificity
Sample Collection
- By nasopharyngeal swab: The sampler gently holds the head of the person to be collected
with one hand, holds the swab with the other hand, sticks the swab
to the nostril to enter, and slowly penetrates backwards along the
bottom of the lower nasal passage, so as not to exert too much
force to avoid traumatic hemorrhage. When the tip of the swab
reaches the posterior wall of the nasopharynx cavity, gently rotate
it for several times (in case of reflex cough, stop for a minute),
and then slowly take out the swab.
- By oropharyngeal swab: The head of the person to be collected is slightly tilted and his
mouth is wide open, exposing the pharyngeal tonsils on both sides.
Wipe the swab across the root of the tongue. Wipe the pharyngeal
tonsils on both sides of the person to be collected back and forth
with a little force for at least 3 times, and then wipe up and down
the posterior pharyngeal wall for at least 3 times.
Test steps
- 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 |
Limitation
1. This reagent is a qualitative detection reagent, which cannot
determine the exact content of antigen.
2. The test results of this reagent are only for the reference of
clinicians and should not be taken as the sole basis for clinical
diagnosis and treatment. Clinical management of patients should be
considered in the light of their symptoms/signs, medical history,
other laboratory tests and treatment responses.
3. Restricted by antigen detection reagent method, the lowest
detection limit (sensitivity analysis) is generally lower than that
of nucleic acid detection, so the researchers deal with negative
result to give more attention, should be combined with other test
results comprehensive judgment, advice to doubt the negative result
of nucleic acid detection or virus isolation culture identification
method for review.
4.False negative results may be caused by unreasonable sample
collection, transport and treatment, and low viral load in samples.
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.