THIS REQUEST FOR INFORMATION (RFI) SOURCES SOUGHT IS ISSUED SOLELY FOR MARKET RESEARCH AND PLANNING PURPOSES ONLY AND DOES NOT CONSTITUTE A SOLICITATION
1. Responses to this Sources Sought must be in writing. The purpose of this Sources Sought Announcement is for market research only to make appropriate acquisition decisions and to gain knowledge of Small Businesses, including Service-Disabled Veteran-Owned Small Businesses and Veteran-Owned Small Businesses (SDVOSB/VOSB), who are interested in submitting proposals for this procurement and who are capable of performing the work required for this procurement.
2. The NAICS for this requirement is 339112 Surgical and Medical Instrument Manufacturing
3. The Contractor shall supply, install, configure, and validate a Mobile Lifting Chair w/ headrest product and provide on-going technical support and maintenance services for that installed product for the Los Angeles VA Medical Center located in Los Angeles, California. The required services (installation, configuration, validation, support, and maintenance for Mobile Lifting Chair w/ headrest) shall be provided by the contractor along with all resources necessary to accomplish the deliverables.
4. Interested and capable Contractors are encouraged to respond to this notice not later than Thursday, July 30, 2026 at 03:00 PM PST, by providing the following information via email only to Hanan.Mccullick@va.gov.
(a) Company name
(b) Address
(c) Point of contact
(d) Phone, fax, and email of primary point of contact
(e) Contractor s Unique Entity ID (SAM) number
(f) Type of small business, if applicable, (e.g. Service-Disabled Veteran-Owned Small Business (SDVOSB), Veteran-Owned Small Business (VOSB), 8(a), HUB-Zone, Woman Owned Small Business, Small Disadvantaged Business, or Small Business).
(g) Statement indicating whether your company is considered small under the size standard for the NAICS code identified under this RFI.
(h) Statement indicating the product name of the Mobile Lifting Chair w/ headrest product referenced above that you intend to provide for this procurement.
(i) Statement indicating whether you are the manufacturer of the Mobile Lifting Chair w/ headrest product that you intend to provide for this procurement. If you intend to provide a Mobile Lifting Chair w/ headrest product manufactured by a company other than your own, state the name of the company whose Mobile Lifting Chair w/ headrest product you intend to provide, the country of origin for the Mobile Lifting Chair w/ headrest product you intend to provide, and whether the company that manufactures that product is a small business under the size standard for the NAICS code identified under this RFI.
(j) Statement indicating if you have a current contract to provide the Mobile Lifting Chair w/ headrest that you intend to provide for this procurement, along with the installation, configuration, validation, support, and maintenance services required by this procurement, under either the General Services Administration s Federal Supply Schedule or with NAC, NASA SEWP, or any other federal contract. If yes, provide the contract type and contract number, as well as the identity of the federal agency with whom you hold that contract.
(k) Statement indicating how many calendar days you estimate it would take you to install, configure, and validate the Mobile Lifting Chair w/ headrest product that you intend to provide for this procurement in a medical center similar to the GLA VA Medical Center.
(l) General pricing for your products/solutions for market research purposes.
(m) A capability statement that provides detailed information for one or more reference contracts that demonstrates your experience providing Mobile Lifting Chair w/ headrest that meets the requirements described in the attached DRAFT Statement of Work and demonstrates your experience providing the installation, configuration, validation, support, and maintenance services required by this procurement. GENERAL STATEMENTS OF CAPABILITY ARE NOT ACCEPTABLE. Respondents must provide the following information for each reference contract the respondent identifies as evidence of the respondent s capability to perform the work required by this procurement. Respondents must provide the following information for each reference contract:
(1) the legal name of entity with whom the respondent held the contract;
(2) the contract number;
(3) a description providing details of the specific tasks the respondent performed under that contract;
(4) the dates during which the respondent performed the contract;
(5) the name, phone number, and email address of a person at the entity with whom the respondent held the contract who can verify the information the respondent provides regarding this reference contract.
If a respondent offers to demonstrate experience through the proposed use of subcontractors, the respondent must identify the legal name of each subcontractor and provide all of the information required above for one or more reference contracts performed by each subcontractor the respondent intends to use.
NOTE: The information requested above is required for the Government to evaluate whether there are sufficient small business concerns of a particular type who are capable of performing the work required by this procurement to determine if this procurement should be set aside for a given type of small business concern. FAILURE TO SUBMIT ALL OF THE INFORMATION REQUESTED ABOVE MAY BE VIEWED BY THE GOVERNMENT AS EVIDENCE THAT THE RESPONDENT LACKS THE ABILITY TO PROVIDE THE MOBILE LIFTING CHAIR W/HEADREST AND SERVICES REQUIRED BY THIS PROCUREMENT. THIS, IN TURN, MAY AFFECT THE GOVERNMENT S DETERMINATION ABOUT WHETHER THE REQUIREMENTS FOR A SET-ASIDE PROCUREMENT HAVE BEEN MET.
5. All Offerors who provide goods or services to the United States Government must be registered in the System for Award Management (SAM) database found at https://www.sam.gov. Registration must include Representations and Certifications.
--End of Sources Sought Announcement--
DISCLAIMER
This RFI is issued solely for information and planning purposes only and does not constitute a solicitation. All information received in response to this RFI that is marked as proprietary will be handled accordingly. In accordance with 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.
SCHEDULE OF SUPPLIES (BRAND NAME OR EQUAL TO RAIZER PRO II):
SALIENT CHARACTERISTICS:
Must have Dimensions (L x W x H): Standing - 655mm x 688mm x 1225mm Lying - 1321mm x 688mm x 277mm
Must have a lift weight capacity of 330 lbs.
Must have ability to perform approximately 80 lifts per charge, or 40 lifts at maximum load.Â
Equipped with safety belts and stability features to ensure secure lifting and transfer.
Must be capable of lifting individuals of varying weights, accommodating a wide range of users.
Built with high-quality materials to withstand regular use in healthcare or home settings.
Must have User-Friendly Controls: Intuitive control panel for easy operation, allowing caregivers to lift and lower users smoothly.
Must have easy Maintenance: Designed for straightforward cleaning and maintenance, ensuring hygiene and longevity.
Must have Adjustable Headrest: Provides additional support and comfort for users during lifting and transferring.
Must be Lightweight, compact and foldable, making it easy to transport and store in various environments.
Must have a rechargeable battery, allowing for mobility without the need for a power outlet during use.
The lift must utilize a rechargeable battery to allow operation throughout patient care areas without requiring connection to an electrical outlet during use.
Must Provide additional support and comfort for users during lifting and transferring.
Must have Streamlined cleaning processes that facilitate infection control and maintenance.
Must have long-lasting battery life that supports extended operational periods without frequent recharging.
Must have comprehensive safety features, including automatic locking systems to prevent accidental movement during use.
Must have sturdy frame construction designed to withstand regular use in busy clinical environments.
Must have intuitive control panel that allows for quick adjustments and operation by staff with minimal training.
Must have versatile height adjustment mechanism that accommodates various patient handling scenarios.
The equipment must comply with applicable FDA medical device requirements and recognized healthcare safety standards.
The lift must include patient head support during lifting and be suitable for use following patient falls.
The overall size and weight must permit transport through standard doorways and operation within patient rooms, outpatient clinics, emergency departments, and rehabilitation areas.
The equipment must fold or disassemble into transportable components for storage and transport between patient care areas.
