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Picture of Reagent Kit QIAstat-Dx® Molecular Diagnostic Respiratory SARS-CoV-2 Panel For use with QIAstat-Dx Instrument 6 Tests691223

Reagent Kit QIAstat-Dx® Molecular Diagnostic Respiratory SARS-CoV-2 Panel For use with QIAstat-Dx Instrument 6 Tests691223

Reagent-Kit-QIAstat-Dx®-Molecular-Diagnostic-Respiratory-SARS-CoV-2-Panel-For-use-with-QIAstat-Dx-Instrument-6-Tests691223

SKU #

#1163375

MPN #

691223

Brand

Qiagen LLC

Stock

In Stock

Quantity

100

Features

TEST KIT, SARS-COV 2PNL QIASTAT RESPIRATORY (6TEST/KT) D/S

$607.91 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1163375
Manufacturer # 691223
Brand QIAstat-Dx®
Manufacturer Qiagen LLC
Application Reagent Kit
For Use With For use with QIAstat-Dx Instrument
Form Cartridge
Number of Tests 6 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 60 days
Sample Type Nasopharyngeal Swab Sample
Storage Requirements USP Controlled Room Temperature
Test Name Respiratory SARS-CoV-2 Panel
Test Type Molecular Diagnostic
Time To Results 67 Minute Results
UNSPSC Code 41116205
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  • QIAstat-Dx Respiratory SARS-CoV-2 Panel is a multiplexed nucleic acid test intended for use with QIAstat-Dx system for the simultaneous qualitative detection and identification of multiple respiratory viral and bacterial nucleic acids
  • For in vitro diagnostic use under Emergency Use Authorization (EUA) only: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
  • Intended for use by trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures
  • Multiplex syndromic cartridge detects and differentiates 21 respiratory targets, including SARS-CoV-2 from nasopharyngeal swabs (NPS) eluted in universal transport media (Enterovirus and Rhinovirus are both detected, but not differentiated)
  • Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. section 263a, to perform high complexity and moderate complexity tests
  • Please review the documents under the "More Information" tab prior to purchasing
  • Link to FDA site: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
  • All reagents required for the complete execution of a test run are pre-loaded and self-contained in the QIAstat-Dx Respiratory SARS-CoV-2 Panel Cartridge
  • Kit includes: (6) Individually packaged cartridges containing all reagents needed for sample preparation and multiplex real-time RTPCR, plus Internal Control, and (6) individually packaged transfer pipettes for dispensing liquid sample into the QIAstat-Dx Respiratory SARS-CoV-2 Panel Cartridge
  • Intuitive workflow with less than one-minute hands-on time
  • All wet and dry reagents onboard and room temperature stable
  • Comprehensive qualitative results available in about an hour