-
,for, Item ID-
- #1283198
- Quidel #20518
Respiratory Test Kit QuickVue™ Influenza + SARS 25 Tests CLIA Waived
TEST, QUICKVUE INFLUENZA +SARS(25/KIT 24KT/CS)
Features
- Quick, reliable results for flu and COVID-19 test in only 10 minutes
- The QUICKVUE Influenza + SARS Tests can differentiate between SARS-CoV-2, influenza A and influenza B antigens directly from anterior nares swab specimen
- Simple workflow
- More …
Product Details Email
Product Specifications
| McKesson # | 1283198 |
|---|---|
| Manufacturer # | 20518 |
| Brand | QuickVue™ |
| Manufacturer | Quidel |
| Country of Origin | Unknown |
| Application | Respiratory Test Kit |
| Buy American Act (BAA) Compliant | No |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | (25) Sealed Test Cassettes, (25) Buffer Tubes, (25) Swabs, Tube Holder, Quick Ref Instructions, IFU |
| Number of Tests | 25 Tests |
| Product Dating | McKesson Acceptable Dating: we will ship >= 90 days |
| Purchase Program Type | Standard Purchase |
| Reading Type | Visual Read |
| Sample Type | Anterior Nasal Swab Sample |
| Specialty | Immunoassay |
| Test Format | Cassette Format |
| Test Kit Type | Rapid |
| Test Method | Lateral Flow |
| Test Name | Influenza + SARS |
| Time to Results | 10 Minute Results |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116144 |
Features
- Quick, reliable results for flu and COVID-19 test in only 10 minutes
- The QUICKVUE Influenza + SARS Tests can differentiate between SARS-CoV-2, influenza A and influenza B antigens directly from anterior nares swab specimen
- Simple workflow
- Two-color visual read result
- Actionable results available in as few as 10 minutes
- Outstanding clinical performance with over 99% of negative percent agreement (NPA) and over 85% of positive percent agreement (PPA)
- The QuickVue Influenza+SARS Test is a lateral flow immunochromatographic assay intended for the qualitative detection and differentiation of influenza A, and influenza B nucleoprotein antigens and SARS-CoV-2 nucleocapsid antigen directly in anterior nasal swab samples from individuals with signs and symptoms of respiratory tract infection
- This test is for use by individuals aged 14 years or older testing themselves, or adults testing aged 2 years or older
- All negative results are presumptive and should be confirmed with an FDA-cleared molecular assay when determined to be appropriate by a healthcare provider
- Negative results do not rule out infection with influenza, SARS-CoV-2, or other pathogens
- Positive results do not rule out co-infection with other respiratory pathogens
More Information
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