Rally #188-1-2183
Quidel #20183
QuickVue® Influenza A+B Test (25 Test/KT 12 KT/CS)
QuickVue® Rapid Lateral Flow Test, Influenza A+B, Nasal & Nasopharyngeal Swab, CLIA Complexity Waived, Rx Only
Features
- Identifies and differentiates both influenza Type A or B in positive samples, or reaches negative results in negative samples
- Fast results in 10 minutes
- Accurate detection with nasal/nasopharyngeal swab samples
- Each kit contains everything needed to perform the test, including foam-tipped nasal swabs and Positive and Negative Controls
- Room temperature storage with 24-month shelf life from date of manufacture
A negative test is presumptive, and it is recommended these results be confirmed by viral culture or an FDA-cleared influenza A and B molecular assay. Negative results do not preclude influenza virus infections and should not be used as the sole basis for treatment or other patient management decisions. The test is intended for professional and laboratory use.
Important Note:
- Product is non-returnable; please make sure it is the right product before ordering.
- If put into refrigeration, do not freeze.
- For in vitro diagnostic use.
- Rx Only
Warning: This product can expose you to chemicals known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov.
Rally # | 188-1-2183 |
Manufacturer # | 20183 |
Brand | QuickVue® |
Manufacturer | Quidel |
Country of Origin | United States |
Application | Respiratory Test Kit |
CLIA Complexity | Waived |
Number of Tests | 25 Tests |
Reading Type | Visual Read |
Sample Type | Nasal Swab / Nasopharyngeal Swab |
Specialty | Immunoassay |
Test Format | Test Strip Format |
Test Kit Type | Rapid |
Test Method | Lateral Flow Method |
Test Name | Influenza A + B |
Time to Results | 10 Minute Results |
UNSPSC Code | 41116144 |
Kit Storage Conditions | Room Temperature (15°C to 30°C/59°F to 86°F) |
Internal Controls | Positive and Negative included |
External Controls | Positive and Negative included |
PPA (versus an FDA-cleared influenza A and B molecular assay) | A: 81.5%, B: 80.9% |
NPA (versus an FDA-cleared influenza A and B molecular assay) | A: 97.8%, B: 99.1% |
Shelf Life | 24 months from date of manufacture |
Configurations
Quidel Catalog Number | Description | Kit Size / Case Size |
20183 | QuickVue® Influenza A+B Test Kit | 25 / 12 |
20103 | Nasal Swab Pack | 25 Swabs |
20226 | Nasopharyngeal Swab Pack | 100 Swabs |
20171 | QuickVue Influenza Nasal Swab Transport Tubes | 25 Swabs |
Reagents and Materials Supplied - 20183 (25-Test Kit)
- Individually Packaged Test Strips (25): Mouse monoclonal anti-influenza A and anti-influenza B antibodies
- Reagent Solution (25): Vials with 340 µL of salt solution
- Reagent Tubes (25): Lyophilized buffer with detergents and reducing agents
- Disposable Pipettes (25)
- Sterile Nasal Swabs (25)
- Positive Influenza Type A Control Swab (1): Swab is coated with non-infectious recombinant influenza A antigen
- Positive Influenza Type B Control Swab (1): Swab is coated with non-infectious recombinant influenza B antigen
- Negative Control Swab (1): Swab is coated with heat-inactivated, non-infectious Streptococcus C antigen
- Package Insert (1)
- Procedure Card (1)
Manufacturer Documentations
- Package Insert – Waived - QuickVue Influenza A+B Test
- Technical Bulletin - Multitrans
- Technical Bulletin - Synagis
- CLSI - QuickVue Influenza A+B Test
- Quiz - QuickVue Influenza A+B Test
- Sales Sheet - QuickVue Influenza A+B Test Swabs
- FAQ - QuickVue Influenza A+B Test
- Technical Bulletin - 2021 CDC Human Influenza Virus Panel - Swab
- Sales Sheet - QuickVue Influenza A+B Test
- Technical Bulletin - External QC
- Procedure Card - QuickVue Influenza A+B Test
- SDS - QuickVue Influenza A+B Test
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- Reimbursements Information -
This product maybe reimbursable, depending on various factors including current law and policies. Rally Inc. does not handle these reimbursements; instead, each reimbursement is handled solely between you, the customer, and the manufacturer, QuidelOrtho. Rally Inc. does not oversee these reimbursements. To check eligibility and get your reimbursements, please follow the manufacturer's reimbursements instructions.You can find more informations on reimbursement details here.