One Step Dengue Antigen Rapid Test Infectious Disease Rapid Diagnosis Ns1 Antigen Rapid Test Kit
Dengue NS1 Antigen Rapid Test Kit Specification Intended Use This rapid Test kit is intended for the qualitative detecti
Description
Basic Info
Type | IVD Reagent |
Specificity | >95% |
Sensitivity | >95% |
Accuracy | >95% |
Storage Temperature | 2′-30′ |
Quality Guarantee Period | 24 Months |
Group | All |
Transport Package | Carton |
Specification | 25 Tests/Kit |
Trademark | LABNOVATION |
Origin | China |
Production Capacity | 500000/Day |
Product Description
Dengue NS1 Antigen Rapid Test KitSpecification
Test Item | Dengue NS1 Antigen Rapid Test Kit |
Sample Type | Serum, Plasma, Whole blood |
Products shelf life | 24 months |
Test Speed | Within 15 minutes |
Sample volume | 3 Drop(80-100ul) |
Package | 25 Tests/Kit |
Storage Condition | Store at 2-30ºC |
This rapid Test kit is intended for the qualitative detection of dengue virus NS1 antigen to dengue virus in serum/ plasma / whole blood to aid in the diagnosis of Dengue viral infection.
Main Components
1. 25 Test Cassettes2. 25 Disposable Pipettes3. Specimen Buffer4. Package Insert
Use Instructions1. Take off the outer packing, put the cassette onto the desk with the sample window up.2. Drop 3 drops (80μl-100μl) of serum/plasma/whole blood vertically into the sample well of cassette. If the whole blood sample is thick, add 1 drop (40-50μl) of specimen buffer into the sample well of cassette.3. Observe the test results immediately within 15-20 minutes, the result is invalid after 20 minutes.
Interpretation Of ResultsPOSITIVE:Two distinct red lines appear. One line should be in the control region (C) and the other line should be in the test region (T).NEGATIVE:One red line appears in the control region(C). No apparent red or pink line appears in the test region (T).INVALID:No red 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.
Company
LABNOVATION TECHNOLOGOES, INC was established in 2001 and has been recognized as a "National High-tech Enterprise". The registered capital (including its wholly-owned subsidiaries) is RMB 20 million, and it is one of the earliest companies exporting in vitro diagnostic reagents in China. The product sales network has covered more than 110 countries and regions around the world.It is the first in the industry to pass the ISO9001:2008.ISO13485:2012/AC:2012 quality system TUV certification, and obtain the EU CE certification and FDA certification.The company invests more than 10% of its sales into product research and development, hardware construction and update every year, and 85% of the company's R&D team employees have more than 5 years of industry experience.
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