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Product Details:
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Warranty: | 18 Months | Storage: | 2℃-30℃ |
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Storage Temp: | 2-30℃ | Package: | 20 Tests/Kit |
Specificity: | >90% | Sensitivity: | >90% |
High Light: | NS NP OP Influenza AB Test Kit,OP Influenza AB Test Kit 90% Specificity,ISO13485 flu test kit at home |
Rapid Test Kit SARS-CoV-2 Antigen And Influenza A/B Rapid Test Kit 20 Tests High Quality Rapid Test Kit
Intended Use
The SARS-CoV-2 Antigen & Influenza A/B Rapid Test Kit is intended for the qualitative detection and differentiation of nucleocapsid protein antigens from SARS-CoV-2, influenza type A and influenza type B in the same time directly from nasal/nasopharyngeal (NS/NP) swab, oropharyngeal (OP) swab and saliva specimens from patients with signs and symptoms of respiratory viral infection. It is for professional use only. It is an aid in the diagnosis of the patients with suspected SARS-CoV-2 or influenza infection in conjunction with clinical presentation and results of other laboratory tests.
Specification
Item |
Antigen test strip performance |
Influenza A test strip performance against PCR | Influenza B test strip performance against PCR |
Sensitivity | 98.03% | 93.3% | 97.00% |
Specificity | 100.00% | 91.00% | 96.40% |
Main Components
Use Step
Apply 2 full drops of the treated sample (60μl-70μl) vertically into each of the two sample wells of the test cassette.
Observe the test results immediately within 15~20 minutes, the result is invalid over 20 minutes.
Interpretation Of Result
POSITIVE: The presence of T (T on nCoV /A or B on Flu) and C lines within the reaction window indicate a positive result on SARS-CoV-2 or Flu A and/or B infection or co-infection.
NEGATIVE: One colored line appears in the control region(C). No apparent colored line appears in the test region (T on nCoV /A or B on Flu). 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.
Feature
Cross-reactivity
With human coronavirus 229E, human coronavirus OC43, human coronavirus NL63, adenovirus, human metapneumovirus, parainfluenza virus 1, parainfluenza virus 2, parainfluenza virus 3, parainfluenza virus 4, influenza A, type B Influenza, enterovirus, respiratory syncytial virus, rhinovirus, SARS coronavirus, MERS coronavirus, Haemophilus influenzae, Streptococcus pneumoniae, Streptococcus pyogenes, Candida albicans, Bordetella pertussis, Mycoplasma pneumonia, pneumonia Chlamydia, Legionella pneumophila, etc. have no cross reaction.
With respiratory Syncytial Virus A, measles Virus, Mumps Virus , adenovirus Type 3, parainfluenza Type 2 , partial Pulmonary Virus, human coronavirus OC43, human coronavirus 229E, human herpes virus 6, cytomegalovirus, epstein Barr Virus, enterovirus CA16, rhinovirus, staphylococcus aureus, streptococcus pneumoniae, mycoplasma pneumoniae, parapertussis, chlamydia pneumoniae, escherichia coli, pooled human nasal wash, candida albicans, etc. have no cross reaction.
FAQ
We have the limit order which is 10000, we would like to cooperate with you, don't worry about MOQ, just send us of your what items you want order.
Stock 3-7 days in general. Or please contact us by email for specific lead time base on your order quantities.
Yes, we accept both OEM and ODM for customers.
We can accept EXW, FOB, CIF, etc. You can choose one which is the most convenient for you.
We're Manufacturer.
We usually quote you within 24 hours after we get your inquiry. If you are very urgent to get the quotation. Please call us or tell us in your mail, so that we could regard your inquiry priority.
Contact Person: Ld
Tel: +8613480985156