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This Sources Sought opportunity from Department Of Veterans Affairs was posted on June 30, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

6640--Ultracentrifuge Equipment And Installation

Closed
36C26226Q1040Federal

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The Department of Veterans Affairs is conducting a Request for Information (RFI) and Sources Sought notice to gather market intelligence for the acquisition of an Ultracentrifuge equipment system with installation for the New Mexico VA Medical Center. This action is not a solicitation and does not commit the government to award a contract; responses are strictly for planning and market research purposes under FAR 15.201(e). The procurement targets a brand name or equal product in compliance with FAR 52.211-6, with specific requirements outlined in Attachment B, including a maximum speed of at least 80,000 RPM, compatibility with both fixed-angle and swinging-bucket rotors, quick rotor swap capability, and support for a wide range of future rotor options. The required equipment includes one Beckman Coulter Optima XE-90 Ultracentrifuge, one installation service without training, one Type 70Ti fixed-angle rotor, and one SW41Ti swinging-bucket rotor. Respondents must submit a detailed capabilities statement addressing each salient characteristic, indicate whether they are the manufacturer or authorized distributor, and confirm compliance with the Non-Manufacturer Rule if applicable. Business size classification under NAICS 334516 with a 1,000-employee small business threshold must be disclosed, along with socioeconomic status such as SDVOSB, VOSB, WOSB, HUBZone, or large business designation. Companies must also provide their SAM.gov Unique Entity ID and CAGE code. Compliance with the Buy American Act and the Trade Agreements Act is mandatory, requiring respondents to specify the country of origin for each component, the final assembly location, the percentage of domestic content by cost, and whether the end product qualifies as a domestic end product. The VA also requests information on whether a U.S.-made or designated-country end product is available and whether the manufacturer is U.S.-based. Respondents must address limitations on subcontracting per 13 CFR §125.6, indicate whether their solution is a Commercial Off-The-Shelf (COTS) item, confirm FDA clearance status, and disclose if leasing options are available. Pricing details are requested solely for market research and will not influence any future award decision. The response deadline is July 7, 2026, at 1:00 PM PDT, and submissions must be made via email to the designated contracting specialist. Any information marked as proprietary will be treated confidentially, and

General Info

VA seeks ultracentrifuge suppliers for market research; no contract awarded; compliance and origin details required.

Agency

Department Of Veterans Affairs → 262-NETWORK Contract Office 22 (36C262)View Agency

NAICS

334516 - Analytical Laboratory Instrument ManufacturingView NAICS

Place of Performance

Department of Veterans Affairs New Mexico VA Healthcare System, Albuquerque, NM, 87108, USA

Set-Aside

NONE

Documents

(3)

Beckman Coulter Ultracentrifuge Brand Name or Equal Requirements

DOCXbrand-name-description

Attachment A - Equipment and Company Information

XLSXcontract-document

RFI 36C26226Q1040 Ultracentrifuge Equipment And Installation

DOCXsources-sought

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Timeline

PhaseClosed
Posted

Sources Sought

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → 262-NETWORK Contract Office 22 (36C262)
Contacts1 person available
OfficeGilbert, AZ, 85297, USA
Organization / Agency
Department Of Veterans Affairs → 262-NETWORK Contract Office 22 (36C262)
View Agency Profile
Office AddressGilbert, AZ, 85297, USA
Contacts
Clift DomenContract Specialist

Full Description

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THIS REQUEST FOR INFORMATION (RFI) / SOURCES SOUGHT NOTICE IS ISSUED SOLELY FOR INFORMATION AND PLANNING PURPOSES. THIS IS NOT A SOLICITATION. SUBMISSION OF INFORMATION ABOUT PRICING, DELIVERY, THE MARKET, AND CAPABILITIES IS HIGHLY ENCOURAGED AND ALLOWED UNDER THIS RFI FOR PLANNING PURPOSES IN ACCORDANCE WITH (IAW) FAR 15.201(e). DISCLAIMER This RFI is issued solely for information and planning purposes and does not constitute a solicitation. All information received in response to this RFI that is marked as proprietary will be handled accordingly. IAW FAR 15.201(e), responses to this notice are not offers and cannot be accepted by the Government to form a binding contract. Responders are solely responsible for all expenses associated with responding to this RFI. SOURCES SOUGHT/RFI DESCRIPTION This is NOT a solicitation announcement. This is a Sources Sought Notice / RFI only. The purpose of this Sources Sought Notice / RFI is to gain information about potential qualified sources and their size classification relative to NAICS 334516 (size standard of 1,000 Employees). Responses to this Sources Sought Notice / RFI will be used by the Government to make appropriate acquisition decisions. After review of the responses to this Sources Sought Notice / RFI, further RFIs and/or a solicitation or other announcements may be published. The Department of Veterans Affairs (VA) is seeking sources capable of providing an Ultracentrifuge equipment with installation that can address the attached list of SALIENT CHARACTERISTICS in Attachment B requirements for New Mexico VA Medical Center. This procurement is seeking a brand name or equal product IAW 52.211-6 -- Brand Name or Equal. The list of Salient characteristics is intended to be descriptive, not restrictive, of the supplies/services that are required. If your company is interested and capable of providing the required supplies/services, please provide the information in Attachments A & Attachment B as well as information indicated below. Response to this notice should include company name, address, point of contact, size of business pursuant to the following questions: (1) Submit your capabilities statement illustrating how your organization can/cannot meet the list of SALIENT CHARACTERISTIC requirements. For instances where your company cannot meet the SALIENT CHARACTERISTIC requirement(s), please explain. For instances where your company can meet the SALIENT CHARACTERISTIC requirement(s), please show how your company meets/exceeds each requirement. (2) Please review the list of SALIENT CHARACTERISTIC requirements and provide any additional feedback or suggestions. If none, please reply as N/A. In the VA s efforts to procure domestic end products, are you able to provide a domestic product or a domestic alternative product? (4) Please indicate the size status and representations of your business, such as but not limited to: Service-Disabled Veteran-Owned Small Business (SDVOSB), Veteran-Owned Small Business (VOSB), HUBZone, Woman Owned Small Business (WOSB), Large Business, etc. (5) Is your company considered small under the NAICS code identified in this RFI? (6) Are you the manufacturer, authorized distributor, and/or can your company provide a solution to the required supplies/services described in the list of SALIENT CHARACTERISTICS? (7) If you are a large business, do you have any designated/authorized distributors? If so, please provide their company name, telephone, point of contact and size status (if available). (8) If you re a small business and you are an authorized distributor/reseller for the items identified above, do you alter; assemble; modify; the items requested in any way? If you do, state how and what is altered; assembled; modified. (9) Limitations on Subcontracting: How does your business ensure compliance with the limitations on subcontracting as outlined in 13 CFR § 125.6? (10) Are the items you are identifying/providing considered Commercial of the Shelf (COTS) items as defined in FAR Part 2.101 under commercial items? (11) Non-Manufacturer Rule: If applicable, can you confirm your business complies with the Non-Manufacturer rule? Specifically, does your company: Provide a product from a small business manufacturer or processor? Not exceed 500 employees? Primarily engage in the retail or wholesale trade and normally sell the type of item being supplied? Take ownership or possession of the item(s) with its personnel, equipment or facilities in a manner consistent with industry practice? (12) What is your lead time to deliver a single unit with all components? Is there scale in lead time with greater quantities? Please elaborate. (13) What is estimated life span of your solution? What support/services does that entail? (14) Does your proposed equipment have FDA clearance? Please specify what FDA clearance(s) have been obtained. (15) Does your organization offer a leasing solution? Please elaborate. (16) Does your company have a Federal Supply Schedule (FSS) GSA/NAC/SAC/BPA/NASA SEWP or any other Federal Government contract? If so, please provide the contract number(s). (17) If you are an FSS GSA/NAC/SAC/BPA/NASA SEWP or any other Federal Government contract holder, are all the items/solutions you are providing information about available on your schedule/contract? Please state if all or some items are available on the contract. (18) General pricing of your products/solution is encouraged. Pricing will be used for the purpose of market research only. It will not be used to evaluate for any type of award. (19) Please provide your SAM.gov Unique Entity ID/Cage Code number. Buy America Compliance Respondents shall provide sufficient detail to determine compliance with the Buy American Act, including country of origin, domestic content, and availability of domestic alternatives. Responses should be complete and supported with verifiable information. Please identify the country of origin for the end product(s) being offered. Include the location of final assembly/manufacture.
Please provide the percentage of domestic content (by cost) for each product(s). Describe the origin of the major components.
Does your product qualify as a domestic end product in accordance with the Buy American Act?
Please identify the manufacturer name and location for the product(s). Confirm whether the manufacturer is U.S.-based.
Identify the country of origin of each product and indicate whether the product qualifies as a U.S.-made or designated-country end product in accordance with the Trade Agreements Act Responses to this notice shall be submitted via email to clift.domen@va.gov. Telephone responses will not be accepted. Responses must be received no later than Tuesday, July 7th, 2026, by 1:00 PM PDT. All responses to this Sources Sought/RFI will be used for planning purposes only. Responses to this Sources Sought Notice / RFI are not considered a request to be added to a prospective bidders list or to receive a copy of the solicitation. If further RFIs and/or a solicitation or other announcement is issued as a result of the information provided from this RFI, all interested parties must respond to the specific posting separately IAW the specifications of that announcement.

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Medical Laboratories

POSTED

1 day ago

DEADLINE

in 6 days
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