1.0 DESCRIPTION THIS IS A SOURCES SOUGHT NOTICE ONLY. This is not a solicitation for bids, proposals, proposal abstracts, or quotations. The Department of Veterans Affairs (VA) Enterprise Procurement Office (EPO), formerly the Strategic Acquisition Center (SAC), is issuing this Sources Sought Notice as a means of conducting market research to identify qualified sources with the capability and resources to meet the Veterans Health Administration s (VHA) Non-Expendable Equipment National Program requirement for Scanning Systems Ultrasonic Portable. The EPO in conjunction with VHA is seeking qualified sources capable of supplying the brand name or equal Fujifilm® Sonosite Scanning Systems Ultrasonic Portable machines on an agency-wide basis. VA is contemplating the award of a single Requirements Contract with Firm-Fixed Price (FFP) orders IAW FAR 16.503, Requirements Contracts, to a supplier of this equipment. Respondents will be required to deliver complete ultrasonic scanning systems to VA medical centers and facilities throughout the United States. The associated North American Industry Classification System (NAICS) code for this procurement is 334510 Electromedical and Electrotherapeutic Apparatus Manufacturing and the associated size standard is 1,250 employees. The FAR Provision found at 52.204-7 requires that The Offeror shall have an active Federal Government contracts registration in the System for Award Management (SAM) when submitting an offer or quotation. You may access the SAM website at SAM.gov | Home. All respondents must be certified with the appropriate NAICS code on the SAM website. All SDVOSB/VOSB respondents must be verified in the SBA database at: https://www.sba.gov/veterans/#vetcert at the time of submission. Submissions for this Sources Sought Notice shall be submitted by email no later than October 19, 2026, at 12:00pm Eastern Time to the Contract Specialist and Contracting Officer at the following email addresses: Alanna.Wilson@va.gov Anthony.Zibolski@va.gov Email responses shall include the following subject line: Response to Sources Sought Notice 36C10X27Q0004. This notice is for planning purposes only and does not constitute a commitment on the part of the Government to award a contract, nor does the Government intend to pay for any information submitted as a result of this notice. This notice is part of a continuous process for obtaining the latest information on the commercial status of the industry with respect to their current and near-term abilities. The information provided herein is subject to change and in no way binds the Government to solicit for, or award, a competitive contract. It is emphasized that this is a notice solely for planning and informational purposes. Respondents are advised that the Government is under no obligation to acknowledge receipt of the information received or provide feedback to respondents with respect to any information submitted. The Government may or may not issue a solicitation as a result of this notice. There is no solicitation available at this time. 2.0 SCOPE OF WORK Scanning Systems Ultrasonic Portable are compact devices that use high frequency sound waves for real-time internal body imaging. Point-of-care ultrasound (POCUS) imaging is routinely used by medical clinicians to guide interventional percutaneous procedures such as vascular access, nerve blocks, and therapeutic injections. Ultrasonic scanning systems have an ultrasonic scanner, transducers (frequencies of 2 to 12 MHz are typical for vascular and abdominal scanning, procedure guidance, and nerve blocks), dedicated software, DICOM software for PACS compatibility and image storage, and an image recorder. Most ultrasonic scanners include continuous-wave and pulsed-wave Doppler capabilities (including a spectrum analyzer) for sensing the velocity and location of blood flow; they can be operated in multiple modes, including color flow mapping mode and triplex mode (i.e., simultaneous acquisition and display of 2-D gray-scale, spectral Doppler, and color flow data). Ultrasonic scanning systems usually display images of the vessels in conjunction with spectrum analysis to depict the vessel and its obstructions. Some ultrasonic scanners use a low frequency (typically 2 MHz) Doppler transducer to obtain the blood flow velocity recording in the intracranial arteries. These systems are used for transdermal examinations and diagnosis of diseases, occlusions, and obstructions in the peripheral vascular system, including a profile of the blood-flow velocity in the area under examination. Most of them also include capabilities for small-part examinations. The following Contract Line Items (CLINs) are being considered: Contract Line Items Manufacture Part Number Description 0001 Sonosite L22916 Transducer, L12-3 0002 Sonosite L23117 Transducer, C10-3 0003 Sonosite L23119 Transducer, C5-1 0004 Sonosite L23120 Transducer, L15-4 0005 Sonosite L23121 Transducer, IC10-3 0006 Sonosite L23972 Transducer, L19-5 0007 Sonosite L24087 Transducer, P5-1 0008 Sonosite L25100 Sonosite PX Ultrasound System 0009 Sonosite L25110 Sonosite PX Stand 0010 Sonosite L25200 Printer, B and W Hybrid Graphic, SONY UP-X898MD 0011 Sonosite L27766 T8-3 ULT-2020 Ultrasound Leakage Tester Kit 0012 Sonosite L28354 Sonosite LX Ultrasound System 0013 Sonosite L29076 Sonosite ECG Module 0014 Sonosite L29465 Transducer, T8-3 12 Months - Standard Coverage Warranty 0015 Sonosite L29671 Transducer, P11-3 0016 Sonosite L30229 Transducer, T8-3 POCUS Bundle -12 Months - Standard Coverage Warranty 0017 Sonosite L30257 Transducer, L13-6 0018 Sonosite L31500 Sonosite ST Ultrasound System 0019 Sonosite L33270 Transducer, UHF46-20 MHz Ultra High-Frequency -12 Months - Standard Coverage Warranty 0020 Sonosite P31199 Steep Needle Profiling, Sonosite ST 0021 Sonosite P31440 Sonosite Voice Assist -12 Months - Standard Coverage Warranty 0022 Sonosite P31987 Small Basket 0023 Sonosite P31988 Large Basket 0024 Sonosite P32357 - Sonosite PIV Assist Sonosite PIV Assist 0025 Sonosite P32441-SVCCON Point of Sale Warranty Plus (2 years), PX System 0026 Sonosite P32442-SVCCON Point of Sale Warranty Plus (2 years), LX System 0027 Sonosite P32443-SVCCON Point of Sale Warranty Plus (2 years), ST System 0028 Sonosite P32444-SVCCON Point of Sale Warranty Plus (2 years), PX/LX/ST/MT Transducers (Not applicable for the T8-3 or UHF46x Transducers) 0029 Sonosite Sonosite Institute for Point-of-Care Ultrasound Exclusive access to over 100 hours of education including courses, videos, webinars, quizzes, certificates and additional resources. Accessible via desktop, tablet or phone. (Included) Respondents should identify a complete solution including associated accessories, as required for full functionality. The following Salient Characteristics (SCs) are being considered: CLINs 0001-0013, 0015, 0017, 0020 apply to the following SC 1-9 CLINs 0014, 0016, 0019, 0021 apply to the following SC 10 CLINs 0026-0028 apply to the following SC 12 CLIN 0029 applies to the following SC 11 SC # SALIENT CHARACTERISTICS METHOD OF EVALUATION SC 1 Multiple configurations of the devices Literature Review SC 2 Must have High-quality image resolution1280 x 1024 pixels or higher Literature Review SC 3 Must have multiple Doppler modes to include color, and continuous Wave Literature Review SC 4 Must have 120V and Battery powered capability Literature Review SC 5 Must have a Phased Array Probe with a low frequency range of between 1-5 MHz Literature Review SC 6 Must have Endocavitary Probe with a frequency range between 2-12.5 MHz Literature Review SC 7 Must have Low to Mid Probe with a frequency range of at least 2-12 MHz Curvilinear Probe Literature Review SC 8 Must have Linear Probe with a frequency range greater than 12 MHz Literature Review SC 9 Must have needle visualization enhancement Literature Review SC 10 Must have a minimum one-year warranty Literature Review SC 11 Must provide Operator training Literature Review SC 12 Must provide Extended Service and Support plan Literature Review SC 13 Must be FDA approved FDA Letter SC 14 Must have Intraoperative system capable of interfacing with VA Electronic Health Record System Literature Review For each product identified in the response (brand name and part number), the response must include descriptive literature demonstrating that the product meets or exceeds the SCs specified above. The Government's intent is to include all ancillary items necessary to ensure the equipment can function as designed by the OEM and as required. Respondents are encouraged to identify any additional accessory, service, or configuration that may be necessary or beneficial to the functionality of the contemplated system. These items must be clearly identified by brand name and part number. In addition to the above CLINs and salient characteristics, the Government contemplates utilizing the below evaluation subfactors: Safety The device will be assessed for patient safety features, including, but not limited to, the following areas: Infection control Thermal injuries Probe maintenance Battery failure procedures Design Design features and functions of the offered device will be evaluated. Areas include but are not limited to the following: Durability of the system and the probes Display screens usability Barcode software to ID patients and physicians Low-Profile wheelbase to assist getting closer to patient Cordless charging station Number of Transducer ports Simplicity of system design for operator (ergonomics, easy setup, User-friendly software applications, reporting, and touch screen ease of use) Performance The device will be evaluated for its ability to perform its intended function. Areas include but are not limited to: Capabilities to support multiple medical services Batter run time Provided Installation Needle guidance system Quality/Construction/Training Extended Warranty Training Secure Data encryption HIPPAA/GDPR compliant Meets ANSI/AAMI ES6061 Electromechanical safety standards Responses to this Sources Sought Notice shall include the following: Full name and address of company. SAM Unique Entity Identifier (UEI). Business Size and socioeconomic status, if applicable (e.g., SDVOSB, VOSB, WOSB, HUBZone, 8(a)). Manufacturer or Distributor: If distributor, provide the full name, business size and address of the manufacturer. If distributor, provide evidence that your firm is currently an authorized distributor for the manufacturer of the products proposed, e.g. an authorized distributor letter with current date certified by the OEM. Country of Origin designation for all products proposed. Describe the firm s ability to provide uninterrupted supply of products on a national scale. Technical literature clearly demonstrating that the proposed product(s) meets the identified salient characteristics identifying the page number(s) where each requirement is met. Does respondent offer an annual service plan, Yes or No? If Yes: Describe what the plan covers? Identify whether the plan covers software updates, parts repair/replacement, or both Provide literature or other documentation describing the service plan. Identify whether service is provided by the OEM or a subcontractor. Identify any additional product, accessory, service, or configuration that may be necessary or beneficial to the functionality of the contemplated system. Include the applicable brand name and part number. Item pricing information of products, inclusive of flat rate shipping. Include any quantity discounts, noting at what order quantity the Government should expect tiered price reductions, if any. NOTE: In order for the Contracting Officer to determine whether a set-aside can be pursued, it is essential to provide pricing information. Without this information, the Contracting Officer will be unable to assess whether there is a reasonable expectation of receiving fair and reasonable pricing from socio-economic concerns. Does your firm anticipate any subcontracting opportunities for this requirement? If yes, identify the type and approximate scope of work that could be subcontracted. Identify any federal contract vehicles held by your firm through which your firm can provide this equipment. Are there any further standards or criteria VA should consider in a procurement action for this equipment? Are the Government s specifications unduly restrictive? If yes, identify the specific requirement(s) considered unduly restrictive and provide supporting rationale and recommended alternative language. Any additional information the Government should know prior to issuing a solicitation. Describe any minimum order quantities, geographic limitations, delivery constraints, lead times, or other limitations that could affect the firm's ability to support the requirement on a nationwide basis.
