6515--600-25-3-441-0813 LASER HANDPIECE 36C26225Q1460

THIS REQUEST FOR INFORMATION (RFI)/SOURCES SOUGHT/RFI IS ISSUED SOLELY FOR INFORMATION AND PLANNING PURPOSES ONLY. THIS IS NOT A SOLICITATION. THE SUBMISSION OF PRICING, CAPABILITIES FOR PLANNING PURPOSES, AND OTHER MARKET INFORMATION IS HIGHLY ENCOURAGED AND ALLOWED UNDER THIS RFI IN ACCORDANCE WITH (IAW) FAR 15.201(e). 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. 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/RFI only. The purpose of this Sources Sought/RFI is to gain knowledge of potential qualified sources and their size classification relative to NAICS 339112 (size standard of 1,000 Employees). Responses to this RFI/Sources Sought Notice will be used by the Government to make appropriate acquisition decisions. After review of the responses to this RFI/Sources Sought Notice, further RFIs and/or a solicitation or other announcements may be published. The Department of Veterans Affairs (VA), VISN 22 Long Beach Network Contracting Office is seeking sources capable of providing Laser Handpiece for the VA Long Beach Healthcare System that can address the draft salient characteristics described below. Brandname Information: Manufacturer & Part Number(s): Candela Corp, 7123-00-0191 Type: 785 Handpiece Assembly Equal to product name: Laser Handpiece Salient Characteristics: Wavelength Function Must operate at 785-nanometer wavelength 5 nanometers, which is effective for treating pigmented lesions and tattoos, especially those with blue or green ink. System Compatibility Must be compatible with a picosecond laser system that delivers energy pulses shorter than 500 picoseconds, allowing for effective treatment with minimal heat damage. Adjustable Spot Sizes Must offer a range of spot sizes between 2 millimeters and 10 millimeters (mm) to allow flexibility when treating different skin types and areas. Power Output Must be capable of delivering at least 0.5 Joules of energy per pulse to treat deep pigmentation while protecting surrounding skin. Control Through Main Unit Must integrate with the laser system s screen or controls so the operator can adjust energy level, pulse speed, and spot size. Cooling System Compatibility Must be compatible with external air-cooling systems, such as Zimmer Cryo units, to improve patient comfort during treatments. Ease of Use Must be lightweight and ergonomically designed, weighing no more than 1.5 pounds, to reduce hand and arm strain during use. Durability Must be made of durable, medical-grade materials and support a lifespan of at least 1 million laser pulses under regular use. Regulatory Approvals Must be FDA-cleared for skin treatments in the U.S. and CE-certified for use in European countries. Automatic System Recognition Must include automatic detection and calibration when connected to the main laser system. The list of draft characteristics is intended to be descriptive, not restrictive, of the supplies and/or services that are required. If your company is interested and capable of providing the required supplies/services, please provide the 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 draft salient characteristics described below. For instances where your company cannot meet the draft salient characteristic(s), please explain. For instances where your company can meet the draft salient characteristic(s), please show how your company meets/exceeds each requirement. (2) Please review the list of draft salient characteristics and provide any additional feedback or suggestions. If none, please reply as N/A. (3) 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. (4) Is your company considered small under the NAICS code identified in this RFI? (5) Are you the manufacturer, authorized distributor, and/or can your company provide a solution to the required supplies/services described in the list of draft salient characteristics? (6) 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). (7) If you re a small business and you are an authorized distributor/reseller for the items identified above, do you alter, assemble, or modify the items requested in any way? If you do, state how and what is altered, assembled, or modified. (8) Limitations on Subcontracting: How does your business ensure compliance with the limitations on subcontracting as outlined in 13 CFR 125.6? (9) Are the items you are identifying/providing considered Commercial of the Shelf (COTS) items as defined in FAR Part 2.101 under commercial items? (10) 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? (11) Please indicate whether your product conforms to the requirements of the Buy American Act? If you are unsure, please state the country of origin for each item. (12) What is your lead time to deliver all items? (13) Does your proposed equipment have FDA clearance (if needed)? Please specify what FDA clearance(s) have been obtained. (14) 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). (15) 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. (16) 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. (17) Please provide your SAM.gov Unique Entity ID number. Responses to this notice shall be submitted via email to Emiljan.Golemi@va.gov. Telephone responses will not be accepted. Responses must be received no later than Thursday, September 4, 2025, by 4:00 PM PST. All responses to this RFI/Sources Sought will be used for planning purposes only. Responses to this RFI/Sources Sought Notice 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 because of the information provided from this RFI, all interested parties must respond to the specific posting separately in accordance with the specifications of that announcement.