Texas Bids > Bid Detail

Notice of Intent to Sole Source Xpress, COV-2/Flu/RSV Plus and Xpress, SARS-COV-2 Plus Test Kits

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Agency: VETERANS AFFAIRS, DEPARTMENT OF
Level of Government: Federal
Category:
  • 66 - Instruments and Laboratory Equipment
Opps ID: NBD00159695690251120
Posted Date: May 3, 2023
Due Date:
Solicitation No: 36C25723D0038
Source: https://sam.gov/opp/fca31337c5...
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Notice of Intent to Sole Source Xpress, COV-2/Flu/RSV Plus and Xpress, SARS-COV-2 Plus Test Kits
Active
Contract Opportunity
Notice ID
36C25723D0038
Related Notice
36C25723Q0234
Contract Line Item Number
10
Department/Ind. Agency
VETERANS AFFAIRS, DEPARTMENT OF
Sub-tier
VETERANS AFFAIRS, DEPARTMENT OF
Office
257-NETWORK CONTRACT OFFICE 17 (36C257)
Award Details
  • Contract Award Date: May 02, 2023
  • Contract Award Number: 36C25723D0038
  • Task/Delivery Order Number: 36C25723N0271
  • Contractor Awarded Unique Entity ID: W6HQTMWB9Q28
  • Contractor Awarded Name: CEPHEID
  • Contractor Awarded Address: Sunnyvale , CA 94089-1189 USA
  • Base and All Options Value (Total Contract Value): $1,400,000.00
General Information
  • Contract Opportunity Type: Award Notice (Original)
  • All Dates/Times are: (UTC-04:00) EASTERN STANDARD TIME, NEW YORK, USA
  • Original Published Date: May 03, 2023 10:56 am EDT
  • Inactive Policy: 15 days after contract award date
  • Original Inactive Date: May 17, 2023
  • Initiative:
    • None
Classification
  • Original Set Aside:
  • Product Service Code: 6640 - LABORATORY EQUIPMENT AND SUPPLIES
  • NAICS Code:
    • 325413 - In-Vitro Diagnostic Substance Manufacturing
  • Place of Performance:
    Harlingen , TX 78550
    USA
Description



    1. Texas Valley Costal Bend Health Care System (TXVCB) has a need for the SARS-COV-2 PLUS and COV-2/FLU/RSV PLUS test kits compatible with the Cepheid Instrumentation. The COVID19 test kits are the only approved FDA Emergency Use Authorization that is exclusively made to work on the current VCB owned Cepheid Analyzers. The SARS CoV-2 and the SARS-CoV-2/Flu/RSV test kits are a rapid, multiplexed real-time RT-PCR test intended for the simultaneous qualitative detection and differentiation of SARS-CoV-2, influenza A, influenza B, and respiratory syncytial virus (RSV) viral RNA in either nasopharyngeal swab, nasal swab or nasal wash/aspirate specimens collected from individuals suspected of respiratory viral infection consistent with COVID-19 by their healthcare provider suspected of COVID-19 by their healthcare provider, pursuant to Section 564 of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. §360bbb-3). The COVID and COVID/FLU/RSV is for use only under EUA in the United States (U.S.) in laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, to perform high complexity tests.




Attachments/Links
Contact Information
Contracting Office Address
  • 2301 E. LAMAR BLVD
  • ARLINGTON , TX 76006
  • USA
Primary Point of Contact
Secondary Point of Contact


History

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