Labnovation Technologies, Inc.
| Payment Terms | T/T, D/A, D/P |
| Supply Ability | 500000/Day |
| Delivery Time | 5-7 work day |
| Packaging Details | Carton |
| Storage | 2℃-30℃ |
| Humidity | ≤60% |
| Sunshine | Not Allowed |
| Frezze | Not Allowed |
| Test Time | 10 |
| Package | 1 Test / Kit |
| Brand Name | LABNOVATION |
| Model Number | LX-401602 |
| Certification | ISO13485,ISO9001 |
| Place of Origin | China |
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Product Specification
| Payment Terms | T/T, D/A, D/P | Supply Ability | 500000/Day |
| Delivery Time | 5-7 work day | Packaging Details | Carton |
| Storage | 2℃-30℃ | Humidity | ≤60% |
| Sunshine | Not Allowed | Frezze | Not Allowed |
| Test Time | 10| Package |
1 Test / Kit |
|
| Brand Name | LABNOVATION | Model Number | LX-401602 |
| Certification | ISO13485,ISO9001 | Place of Origin | China |
| High Light | 1T saliva rtk test kit ，15 Min saliva rtk test kit ，10 Min salixium rapid test kit | ||
Rapid Antigen Test Kit CoV-19 Antigen Saliva Rapid Test Self Test 1 Test High Accuracy Easy Use Test Kit
Intend Use
SARS-CoV-2 antigen saliva rapid test kit is intended for the qualitative detection of SARS-CoV-2 antigen in human saliva sample from novel coronavirus suspected person with symptoms within 9 days from onset. The test result can be used for early detection and triage of people suspected of being infected.Further nucleic acid detection should be carried out for suspected population whose antigen test result is positive or negative.
Product Details
| Item | Value |
| Name | SARS-CoV-2 Antigen Saliva Rapid Test Kit (Self Test) |
| Model Number | LX-401602 |
| Type | 1 Test |
| Warranty | 18 Months |
| Power Source | Instruction Manual |
| Quality Certification | CE |
| Safty Standard | ISO13485 |
| Sample Type | Saliva |
| Sample volume | 3 Full drops |
| Test Speed | Within 10-15 minutes |
| Total Accuracy | Over 95% |
| Sensitivity | 94.29% |
| Specificity | 99.00% |
Product Feature
Advantage
Main Components
Use Step
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). The negative result does not indicate the absence of analytes in the sample, it only indicates the level of tested analytes in the sample is less than the minimum detection limit.
INVALID: No colored lines appear, or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.
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. |
Precaution
Company Details
Business Type:
Manufacturer
Year Established:
2001
Total Annual:
10000000-50000000
Employee Number:
100~600
Ecer Certification：
Active Member
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 reagent... 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 reagent...
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