Product Details
Rapid Antigen Test Kit COVID-19 Antigen Rapid Test Kit High Quality
Simple Operate Professional Use Rapid Antigen Test Kit
Intend Use
This rapid test kit is intended for the qualitative detection of
SARS-CoV-2 infection from patients. It is for professional use
only. 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.
Product Details
Item | Value |
Product Name | SARS-CoV-2 Antigen Rapid Test Kit |
Model Number | LX-401301 |
Type | 20 Tests/Kit |
Sensitivity | 98.04%, |
Specificity | 100% |
Total Accurracy | > 99% |
Warranty | 24 Months |
Quality Certification | CE |
Safty Standard | ISO13485,MSDS |
Sample Type | Nasal, Oropharynx Swab |
Sample volume | 3 Full drops |
Test Speed | Within 10-15 minutes |
Product Advantage
- Simplicity: It is extremely easy to use with simple to understand
instructions.
- Fast: After the extraction of the sample, it will take just 10-15
mins for the result to be reflected on the testing device.
- Reliable: CE, ISO13485 Certificated, Stric quality control, High
quality
- Extraction tube is fully enclosed for disposal
Main Components
- 20 Test Cassettes
- 20 Sample tubes
- 2 Sample extraction buffers
- 20 Swabs
- 1 Package Insert
Use Step
- 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
Application
- Suspected population(Families and close contacts of confirmed or
suspected cases)
- High-risk groups(the elderly and children with basic illness or
people with poor immunity)
- Center for Disease Control and Prevention
- Primary Health Care Institution
Limitations
- This reagent is a qualitative detection reagent, which cannot
determine the exact content of antigen.
- 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.
- 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.
- False negative results may be caused by unreasonable sample
collection, transport and treatment, and low viral load in samples.
FAQ
We have the MOQ limit, which is 10000 pieces.
- What the certification you have?
CE, ISO9001, ISO13485
After order confirmed, we will arrange your order immediately, and
offer you an estimated delivery date.
Yes, we accept OEM / ODM.
Air cargo or Ocean cargo.
Business to business account.
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.