Description
QuickVue At-Home Test Kit
Exp Date: January 2025 (Rapid Results In 10 Minutes) The QuickVue At-Home OTC COVID-19 Test by Quidel Corporation is a rapid test that is defined as a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 also known as COVID-19. The Antigen test is authorized by the FDA as a non-prescription home use with self-collection direct anterior nasal (nares) swab samples from individuals aged 14 years or older with symptoms of COVID-19 within the first six days of symptom onset. This Quickvue At Home Antigen Test 2pk test is also authorized for non-prescription home use with adult-collected anterior nasal swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first six days of symptom onset. The manufacturer of the test is Quidel Corporation located within the United States. Peach Medicalis is an authorized distributor of Quidel products. Purchase Quickvue Self Test Online with confidence. Please call us at 1-877-597-3224 or e-mail us at sales@peachmedical.com for wholesale pricing on Quickvue Covid Tests. We are happy to provide references in theatre, government, banking, education, fortune 500 companies, and 50,000+ orders of test kits sold over the past year.
The Accuracy of Quickvue Covid Test Accuracy Self Antigen Test
In a clinical study, the QuickVue At-Home OTC COVID-19 Test identified positive cases 83.5% of the time, and identified negative cases 99.2% of the time (83.5% PPA, and 99.2% NPA, respectively), when compared to the PCR Test. For more information on comparing Antigen Tests and PCR test, please check out our recent article.
- Results: 10 Minutes
- Specificity: 83.5%
- Sensitivity: 99.2%
Quickvue At-home COVID Test Instructions
The Quickvue At-Home OTC COVID-19 test can accurately detect the Omicron variant (among others) of the Sars-CoV-2, the potentially deadly virus that can lead to COVID-19. Quickvue at home COVID Test Instructions
Quickvue At Home Home Instructional Youtube Video
DISCLAIMER
Please note that all Peach Medical shipments do not require a signature upon delivery. Since most test kits should be stored between 35.6 and 86 degrees F range, we strongly recommend tracking your order and anticipating its delivery. However, if the test is stored outside the temperature range for a relatively short period – for a couple of hours up to a day or two – it will be fine to use as long as the test and its components are used at room temperature. Peach Medical is not responsible if the test kits are left outside in extreme temperatures for longer than the recommended time frame after delivery.
Product Documents
The QuickVue At-Home OTC COVID-19 Test is intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 from individuals within 6-days of symptom onset or individuals without symptoms or other epidemiological reasons to suspect COVID-19 infection when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests. This product has not been FDA cleared or approved; but has been authorized by FDA under an Emergency Use Authorization (EUA) for the Public Health Emergency This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1) unless the declaration is terminated or authorization is revoked sooner. For more information on EUAs please visit the FDA’s Website For the most up-to-date information on COVID-19, please visit the CDC’s Website
