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#1001198984 | Mfg #20387 | Clinical Laboratory

Rapid Test Kit QuickVue® Professional Use SARS Antigen Nasal Swab Sample 25 Tests

TEST KIT, SARS ANTIGEN QUICKVUE PROFESSIONAL USE (GOV)(25/KT
Rapid Test Kit QuickVue® Professional Use SARS Antigen Nasal Swab Sample 25 Tests

For use under an Emergency Use Authorization (EUA) only: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations

Product Specifications

MSFH #
1001198984
Manufacturer #
QuickVue® Professional Use, 20387, Quidel
Brand
(25) Vials of Reagent Solution with 340 µL Salt Solution, (25) Reagent Tubes, (25) Individually Packaged Test Strips, Rapid Test Kit, United States, (25) Sterile Nasal Swabs
Manufacturer
SARS Positive Control Swab
Country of Origin
Negative Control Swab
Application
Package Insert
Contents 1
and Procedure Card
HCPCS
U0002
Number of Tests
25 Tests
Product Dating
MSFH Acceptable Dating: we will ship >= 30 days
Reading Type
Visual Read
Sample Type
Nasal Swab Sample
Test Format
Test Strip Format
Test Method
Lateral Flow Method
Test Name
SARS Antigen
Time to Results
10 Minute Results
UNSPSC Code
41116126

Description

Product ships from MSFH with minimum 30 days dating

Testing 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; this 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

Please see attached letter for detailed information on a 1 year extension on expiration dating

The QuickVue SARS Antigen Test is a lateral flow immunoassay that allows for the rapid, qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in anterior nares (NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first five days of the onset of symptoms

The QuickVue SARS Antigen test does not differentiate between SARS-CoV and SARS-CoV-2

Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status; positive results do not rule out bacterial infection or co-infection with other viruses

Laboratories within the United States and its territories are required to report all results to the appropriate public health authorities

Negative results should be treated as presumptive and confirmation with a molecular assay, if necessary, for patient management, may be performed; negative results do not rule out COVID-19 and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions

Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19

The QuickVue SARS Antigen test is intended for use by trained clinical laboratory personnel and individuals trained in point of care settings

Accurate detection with direct anterior nares swab samples: 96.6% PPA and 99.3% NPA

Simple workflow follows a similar format to CLIA-waved QuickVue assays, just sample, dip, and read

Each kit contains everything needed to perform the test, including Nasal Swabs and positive and negative controls