6515-- Intent to Sole Source-Dual Lumen Cannula RVAD/VV-ECMO
Closed Pre-Solicitation Posted
- Solicitation number
- 36C24624Q0678
- Agency
-
Veterans Integrated Service Network 6
Veterans Health Administration, Department of Veterans Affairs
- Responses due
- Set-aside
- No set-aside
Opportunity facts
- NAICS code
- 339113 Surgical Appliance and Supplies Manufacturing
- Place of performance
- Houston, Texas 77058, United States
- Points of contact
Notice details come from SAM.gov. Updated .
About this opportunity
The Department of Veterans Affairs (VA) intends to award a sole source firm fixed price purchase order to Livanova for Protek Duo, Dual lumen (RVAD/VV-ECMO) cannula products. The Protek Duo cannulas, in sizes 29FR and 31FR, are the only FDA-approved devices capable of providing centrifugal flow and temporary cardiopulmonary bypass functionality required for RVAD and VV-ECMO tasks. The VA will purchase 5 units of each size for the Cardiology Department at the Hunter Holmes McGuire VA Medical Center in Richmond, Virginia. Interested parties must submit capability statements by 12:00 PM EST on April 26, 2024 to the Contracting Officer.
This is a sole source acquisition under FAR 13, with no set-aside designation. The NAICS code is 339112 (Surgical and Medical Instrument Manufacturing) and the PSC code is 6515 (Medical and Surgical Instruments, Equipment, and Supplies). The current incumbent is Livanova, and the total contract value is unknown. The period of performance for this one-time buy is from April 26, 2024 to May 10, 2024.
Notice text
INTENT TO SOLE SOURCE: The Department of Veteran Affairs intends to award a sole source firm fixed price purchase order to Livanova. This purchase order will be for Protek Duo, Dual lumen (RVAD/VV-ECMO), cannula (29FR and 31FR) for the cardiology Department at the Hunter Holmes McGuire VA Medical Central Richmond Virginia.
The Protek Duo provides centrifugal flow throughout the heart; rated up to 5 L/min with sizes, 29 FR and 31 FR. It has the ability to be connected to portable heart pump and/or oxygenator. Its the only approved medical device capable for RVAD and VV-ECMO tasks by the FDA (FDA 510(k) Clearance K232480—Medical Devices).
This proposed contract action is for supplies for which the government intends to solicit and negotiate with only one source under the authority of FAR 13.106-1(b). This notice of intent is not a request for competitive quotations; however, all expressions of interest received within three (3) days of the issuance of this notice will be considered by the government. Interested contractors may identify their capability to provide the services prescribed within this notice and should provide sufficient data for the government to determine them as a comparable alternative to the intended source by sending capability statements in reference to this requirement no later than 12:00 PM EST, April 26, 2024 to: robert.morgan@va.gov.
Files
| File | Type | Posted |
|---|---|---|
| S02. 36C24624Q0678.pdf |
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