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CLARITY COVID-19 Antigen Rapid SwabTest CLIA Wvd 25/Box

CLARITY COVID-19 Antigen Rapid SwabTest CLIA Wvd 25/Box

Code: CLA-COV19AG-VIS
Shipping Weight: 1.00 pounds
BY CLARITY DIAGNOSTICS

COVID-19  RAPID ANTIGEN TEST

*RAPID DIAGNOSTIC TEST FOR THE DETECTION OF SARS-COV-2 ANTIGEN

THIS IS NOT A HOME USE TEST // FOR PURCHASE BY MEDICAL PROFESSIONALS ONLY // UNDER EUA FROM THE FDA

Intended at POC setting (i.e., in patient care settings) by medical professionals operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation
  
YOUR STATUS WILL BE VERIFIED BY OUR STAFF BEFORE ANY TESTS ARE SHIPPED
  • LATERAL FLOW ASSAY
  • POSITIVE RESULTS IN 5 MINUTES, NEGATIVE RESULTS READ AT 10 MINUTES
  • FOR MEDICAL PROFESSIONALS ONLY (SEE ABOVE)
  • DETECTS SARS-COV-2 NUCLEOCAPSID PROTEIN ANTIGEN
  • IDENTIFY ACUTE INFECTION IN SYMPTOMATIC PATIENTS

  • ECONOMICALLY PRICED
  • FDA EUA APPROVED, CLIA WAIVED, AND POCT APPROVED
  • RELATIVE SENSITIVITY: 87.5%
  • RELATIVE SPECIFICITY: 98.9%
  • FAST & EASY (POSITIVE RESULTS AS FAST AS 5 MINUTES)
  • TEST NASO-PHARYNGEAL SWAB (immediately or store at room temp and test within 1 hour)
  • Or NASO-PHARYNGEAL SWAB STORED IN DRY TUBE (at 2-8 degrees C can be tested within 24 hours)
PRODUCT CODE: CLA-COV19AG-VIS (25/BOX)
CONTENTS:
25 Individually Pouched Test Cassettes.  25 Sterile Naso-Pharyngeal Swabs.  25 Buffer Tubes. 1 Negative Control Swab. 1 Positive Control Swab. 1 Work Station.  Package Insert & Quick Start Guide.

CLEAR VISION-CLEAR RESULTS
CLARITY DIAGNOSTICS

THIS TEST PRODUCT IS MADE IN SALO, FINLAND

Please Note:

This product has not been FDA cleared or approved, but has been authorized by FDA under an EUA for use by authorized laboratories/Entities

  • This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and

  • 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.




Price: $295.00
Quantity Ordered: none
Quantity:
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