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| Categories | Antigen Self Test Kit |
|---|---|
| Brand Name: | LABNOVATION |
| Model Number: | LX-401302 |
| Certification: | ISO13485,ISO9001,CE |
| Place of Origin: | China |
| MOQ: | 10000 Pieces |
| Price: | Negotiation |
| Payment Terms: | T/T, D/A, D/P |
| Supply Ability: | 1000000/Day |
| Delivery Time: | Shiping as soon as received payment |
| Packaging Details: | Carton |
| Shelf life: | 24 months |
| Sample Type: | Nasal Specimen |
| Package: | 1 Test/Kit |
| Use: | For self test use |
| Storage Condition: | 2℃-30℃ |
| Test Time: | Within 15 min |
| Group: | Universal |
| Company Info. |
| Labnovation Technologies, Inc. |
| View Contact Details |
| Product List |
SARS-CoV-2 Antigen Rapid Test Kit ISO13485 Certificated Rapid Antigen Diagnostic Test Kit Self Test Use Easy Operation
Intend Use

Product Details
| Item | Value |
| Model Number | LX-401302 |
| Package | 1 Test/Kit |
| Sample volume | 3 Full drops |
| Warranty | 24 Months |
| Quality Certification | CE |
| Safty Standard | ISO13485 |
Diagnostic Accuracy

Product Feature

Main Components

Use Step

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. | others |
WARNINGS AND IMPORTAN INFORMATION
• DISPOSAL The test kit can be disposed of with normal household waste in accordance with applicable local regulations.
• A negative result does not rule out the infection of a SARS-CoV-2 infection. Therefore, the test should not be used as the only reference for the clinical diagnosis. The result must be confirmed by the PCR.
• After use, rinse hands or, in case of contact with the buffer solution, the affected body parts thoroughly with water.
• If symptoms persist: Seek medical advice.
Certificate

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