{"product_id":"respiratory-test-kit-tyfast-flu-a-b-covid-19-multiplex-rapid-test-10-tests-box-of-10-mk-1265431-copy","title":"Respiratory Test Kit Tyfast Flu A+B \/ COVID-19 Multiplex Rapid Test 25 Tests BOX OF 25 MK-1265432","description":"\u003cdiv id=\"specifications\" class=\"row fixed-navbar-item\"\u003e\n\u003cdiv class=\"col-lg-12 col-md-12\"\u003e\n\u003cdiv class=\"row\"\u003e\n\u003cdiv class=\"col-md-6\"\u003e\n\u003ch6 id=\"features\"\u003eFeatures\u003c\/h6\u003e\n\u003cul class=\"product-features\"\u003e\n\u003cli\u003eThe CorDx Tyfast Flu A\/B \u0026amp; COVID-19 Multiplex Rapid Test is only for in vitro diagnostic use under the Food and Drug Administration’s Emergency Use Authorization: https:\/\/www.fda.gov\/medical-devices\/covid-19-emergency-use-authorizations-medical-devices\/in-vitro-diagnostics-euas-antigen-diagnostic-tests-sars-cov-2\u003c\/li\u003e\n\u003cli\u003eProduct ships with minimum 90 days dating\u003c\/li\u003e\n\u003cli\u003eThe CorDx Tyfast Flu A\/B \u0026amp; COVID-19 Multiplex Rapid Test is a lateral flow immunochromatographic assay intended for in vitro rapid, simultaneous qualitative detection and differentiation of influenza A and influenza B nucleoprotein antigens and SARS-CoV-2 nucleocapsid antigen directly from anterior nasal swab specimens of individuals with signs and symptoms of respiratory infection consistent with COVID-19 by their healthcare provider within the first five (5) days of symptom onset when tested at least twice over three days with at least 48 hours between tests\u003c\/li\u003e\n\u003cli\u003eThe test provides an efficient and accurate diagnostic solution in 10 mins, giving healthcare providers and communities a rapid and reliable way to prioritize their health\u003c\/li\u003e\n\u003cli\u003eTesting is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. § 263a, that meet the requirements to perform moderate, high or waived complexity tests\u003c\/li\u003e\n\u003cli\u003eThis test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation\u003c\/li\u003e\n\u003cli\u003eResults are for the simultaneous in vitro detection and differentiation of SARS-CoV-2, influenza A virus, and influenza B virus protein antigens, but do not differentiate, between SARS-CoV and SARS-CoV-2 viruses and are not intended to detect influenza C antigens\u003c\/li\u003e\n\u003cli\u003ePositive results do not rule out bacterial infection or co-infection with other viruses\u003c\/li\u003e\n\u003cli\u003eNegative results do not rule out influenza or SARS-CoV-2 infection, and should not be used as the sole basis for treatment or patient management decisions, including infection control measures such as isolating from others and wearing masks\u003c\/li\u003e\n\u003cli\u003eNegative results should be considered in the context of an individual’s recent exposures, history and the presence of clinical signs and symptoms consistent with each respiratory infection\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2 class=\"page-section h3\" tabindex=\"0\"\u003eProduct Specifications\u003c\/h2\u003e\n\u003chr class=\"bb\"\u003e\n\u003cdiv class=\"row\"\u003e\n\u003cdiv class=\"col-md-6\" tabindex=\"0\"\u003e\n\u003cdiv class=\"table-responsive\"\u003e\n\u003ctable class=\"table table-hover blue\" role=\"presentation\"\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eMcKesson #\u003c\/th\u003e\n\u003ctd\u003e1265432\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eManufacturer #\u003c\/th\u003e\n\u003ctd\u003eACT21001-25\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eBrand\u003c\/th\u003e\n\u003ctd\u003eTyfast\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eManufacturer\u003c\/th\u003e\n\u003ctd\u003eCorDx Inc\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eCountry of Origin\u003c\/th\u003e\n\u003ctd\u003eUnited States\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eApplication\u003c\/th\u003e\n\u003ctd\u003eRespiratory Test Kit\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eBuy American Act (BAA) Compliant\u003c\/th\u003e\n\u003ctd\u003eYes\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eContents 1\u003c\/th\u003e\n\u003ctd\u003e(25) Test Cassettes, (25) Swabs, (25) Tubes with Sample Processing Solution, IFU, Quick Ref Guide\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eNumber of Tests\u003c\/th\u003e\n\u003ctd\u003e25 Tests\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eProduct Dating\u003c\/th\u003e\n\u003ctd\u003eMcKesson Acceptable Dating: we will ship \u0026gt;= 90 days\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003ePurchase Program Type\u003c\/th\u003e\n\u003ctd\u003eStandard Purchase\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eReading Type\u003c\/th\u003e\n\u003ctd\u003eVisual Read\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eSample Type\u003c\/th\u003e\n\u003ctd\u003eAnterior Nasal Swab Sample\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eSpecialty\u003c\/th\u003e\n\u003ctd\u003eImmunoassay\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eTest Format\u003c\/th\u003e\n\u003ctd\u003eCassette Format\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eTest Kit Type\u003c\/th\u003e\n\u003ctd\u003eRapid\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eTest Method\u003c\/th\u003e\n\u003ctd\u003eLateral Flow\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eTest Name\u003c\/th\u003e\n\u003ctd\u003eFlu A+B \/ COVID-19 Multiplex Rapid Test\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eTime to Results\u003c\/th\u003e\n\u003ctd\u003e10 Minute Results\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eTrade Agreement Act (TAA) Compliant\u003c\/th\u003e\n\u003ctd\u003eYes\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth scope=\"row\" class=\"text-nowrap\"\u003eUNSPSC Code\u003c\/th\u003e\n\u003ctd\u003e41116144\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"row\"\u003e\n\u003cdiv class=\"col-md-6\" tabindex=\"0\"\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"CorDx Inc","offers":[{"title":"Default Title","offer_id":46476241993917,"sku":"MK-1265432","price":288.95,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0518\/5971\/8333\/files\/1265431_pkgleft.jpg?v=1772826402","url":"https:\/\/axiommedicals.com\/products\/respiratory-test-kit-tyfast-flu-a-b-covid-19-multiplex-rapid-test-10-tests-box-of-10-mk-1265431-copy","provider":"Axiom Medical Supplies","version":"1.0","type":"link"}