Rapid Antigen Test Kit COVID-19 Antigen Rapid Test 20Test For
Professional Testing Use High Quality Antigen Rapid Test Kit
Intend Use
This is used for in vitro qualitative detection of the antigen of
novel virus in human nasopharyngeal swabs. It is for professional
use only. The test kit in an aid the diagnosis of the patients with
suspected SARS-CoV-2 infection. The test kit performance is
conjunction with clinical presentataion 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/Box |
| Sensitivity | 98.04%, |
| Specificity | 100% |
| Warranty | 24 Months |
| Quality Certification | CE |
| Safty Standard | ISO13485,MSDS |
| Sample Type | Nasal, Oropharynx Swab |
| Sample volume | 3 Full drops |
| Test Speed | Within 15 minutes |
Product Feature
- High accuracy, Specificity and Sensitivity
- Excellent Performance
- One-Step operation without extra instruments
- Safety and Reliability
Application
- Center for Disease Control and Prevention
- Primary Health Care Institution
- School
- Prison / Detention Center etc.
Main Components
- 20 Test Cassettes
- 20 Sample tubes
- 2 Sample extraction buffers
- 20 Swabs
- 1 Instruction for use
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. | |
Certificate
FAQ
- How can I distinguish a good test kit ?
You can judge from 3 facts:
Technical data: Such as the accuracy, specificity and sensitivity.
Pouch sealing: Tight enough. If the foil pouch is not sealed well,
the humidity in circustance will destroy the reactivity of
antibodies labeled on NC membrane. Shelf life will be shorten down.
Background: Good test usually gives clean background after running.
If there are red smears in the reading window, it usually caused by
bad colloidal gold technology or bad NC membrane. Sometimes, the
defect caused false positive result in practice.
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.
Business to business account.
