Autotransfusion Equipment

SOURCES SOUGHT NOTICE REQUEST FOR INFORMATION (RFI)/SOURCES SOUGHT Autotransfusion Cell Saver Equipment THIS IS A REQUEST FOR INFORMATION (RFI) / SOURCES SOUGHT NOTICE ONLY. This is not a solicitation for bids, proposals, proposal abstracts, or quotations. The purpose of this RFI/Sources Sought Notice is for market research purposes only, to obtain information in regards to the availability of specified products, services, or a combination of both products and services, and to identify potential sources capable of providing products or performing services in accordance with the requirements below. Responses to this notice will be used by the Government to make appropriate acquisition decisions. DISCLAIMER: This RFI/Sources Sought Notice is issued solely for information and planning purposes only and does not constitute a solicitation. All information received in response to this RFI/Sources Sought Notice that is marked as proprietary will be handled accordingly. 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. If a solicitation is issued it shall be published at a later date and all interested parties must respond to that solicitation announcement separately from the response to this RFI/Sources sought notice. Responses to this sources sought notice are not a request to be added to a prospective bidders list or to receive a copy of the solicitation. Submission of price, delivery, capabilities, and other market information are authorized. However, responses to these notices are not offers and cannot be accepted by the Government to form a binding contract IAW FAR 15.201(e). The purpose of this sources sought/RFI is to gain knowledge of potential qualified sources and their size classification relative to NAICS 339112. DESCRIPTION: The Department of Veteran Affairs, Network Contracting Office 15 (NCO 15) is seeking sources that can provide Autotransfusion Cell Saver Equipment and disposables in accordance with (IAW) the below requirement and North American Industry Classification System (NAICS) code 339112 (size standard of 1000 Employees). The purpose of this requirement is to purchase autotransfusion cell saver equipment and associated disposable supplies for patient care during surgical procedures at Kansas City VA Medical Center (KCVA). This device enables intraoperative autotransfusion during cases with anticipated blood loss, such as complex vascular procedures. This requirement covers the following: Purchase of autotransfusion cell saver machine. Provision of compatible single use disposable supplies (e.g., collection reservoirs, filters, tubing, anticoagulant syringes, reinfusion bags) compatible with cell saver machine. All preventative maintenance and equipment repair as needed. Training and ongoing clinical support and any equipment manuals. Equipment requirements: FDA-approved autotransfusion cell saver device suitable for intraoperative blood salvage and autotransfusion. Must meet applicable VA standards and regulations for safety and efficacy. Provide fully automated processing of collected blood, including separation, washing, and concentration of red blood cells for reinfusion. Have at least two selectable processing modes, including an emergency/rapid mode and a high-quality (standard) mode, to optimize clinical response. Accept multiple bowl sizes to include 125mL, 175 mL, and 225 mL to allow flexibility. Have automated priming, washing and reinfusion cycle. Have adjustable wash programs for optimal red blood cell salvage and customizable wash volumes. Must be single use, disposable set to ensure sterility. Provide high hematocrit (> 60%) and efficient removal of undesirable plasma, heparin, free hemoglobin, and other contaminants. Feature a large, color touchscreen display, with intuitive menu navigation and programmable protocol settings and built in data recording and storage capability-automatic documentation of case parameters for quality control and download. Have air and blood leak detection with automatic alarms. Secure, closed-circuit design to minimize contamination risk. Mobile, compact, lightweight and have locking wheels for use in various OR settings. Integrated battery backup for several hours of operation in the event of power loss. All patient-contacting components must be single-use, sterile disposables, and compliant with current infection prevention standards. Service: Must provide preventive and on-demand maintenance. Disposables: All necessary single-use consumable items compatible with equipment, including: Blood collection reservoirs Bowl sets required per case type Aspiration and anticoagulation line AAL ¼ suction assemblies Reinfusion bags Procedure sets required per case type Filters Anticoagulation syringes Compliance: All equipment and disposables must meet relevant VA, OSHA, and FDA standards and guidelines. Deliverables: Cell saver equipment installed and maintained. Disposable consumable supplies. VENDOR RESPONSE If you are interested and are capable of providing the sought-out supplies/services, please provide the requested information as well as the information indicated below. 1. Company Name: 2. Company Address: 3. SAM UEI: 4. Company POC: 5. Phone Number: 6. EMAIL: 7. Is your company considered a small business IAW the NAICS identified in this RFI/Sources Sought Notice? If so, 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.)? 8. If your company is considered a large business, does your company have any authorized small business distributors/suppliers, service providers, and/or does your company sub-contract to small business concerns? If so, please provide the company name, company POC, and small business status (if available): 9. Is your company an authorized distributor/supplier and/or service provider (or equivalent) of the products and/or services identified in this sources sought? If so provide authorization letters and/or agreements from manufacturer. 10. Does your company alter, modify, or change the products identified in this sources sought? If so, please identify how the products are altered, modified, or changed. 11. Provide the country where the products are manufactured. 12. Does your company currently hold a Federal Supply Schedule (FSS) contract with GSA, the VA National Acquisition Center (NAC), NASA SEWP, VA Strategic Acquisition Center (SAC), or have any other federal contract that can be utilized to procure the products and/or services identified in this sources sought? 13. Please submit a capabilities statement that provides clear, compelling, and convincing evidence that your company can meet the requirements outlined in this sources sought. Responses to this notice shall be submitted via email to Tracie Raggs at tracie.raggs@va.gov. Telephone responses shall not be accepted. Responses must be received no later than Friday, July 17, 2026, at 0800 CST.