Rapid Test Kit CoV-19 Antigen Rapid Test Kit 20 Test Professional
Diagnosis High Accuracy Rapid Antigen Test Kit
Intend Use
The SARS-CoV-2 antigen rapid test kit is intended for professional
detection sars-cov-2 antigen in infection human nasopharyngeal or
oropharyngeal swab, the test provides preliminary test results.
It's an aid inthe diagnosis of the patients with suspected
SARS-CoV-2 infection in conjunction with clinical presentation and
results of other laboratory tests. To be attention the test result
should no be used as the sole basis for diagnosis.
Product Details
| Item | Value |
| Brand | Labnovation |
| 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 |
| Power Source | Instruction Manual |
| Quality Certification | CE |
| Safty Standard | ISO13485,MSDS |
| Sample volume | 3 Full drops |
| Test Speed | Within 15 minutes |
Product Feature
Short test time, get the result within 10-15 minutes
Easy operation, specimen is easy to collect, one-step solution
Lower cost with high effeciency
Advantage
- Latest design which uses faster and moe convenient operation
- Fast recation, test accuracy up to 99%
- Sampling swab, designed for more specimen collection and relase
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.
- How can I do, if some urgent questions?
If you have any questions, you can call us or send us by email or
whatsapp.
- What the certification you have?
CE, ISO9001, ISO13485
- Will you help me register the products in my country ?
Sure, we will provide all you documents and samples you need for
register.
