Inactive

GENERAL SPECIFICATIONS FOR REPAIR AND UPGRADE OF SIMULATION MANNEQUIN FOR SIMULATION LAB Background The Laredal SimManikin system is used for simulation and training for various clinical procedures an... GENERAL SPECIFICATIONS FOR REPAIR AND UPGRADE OF SIMULATION MANNEQUIN FOR SIMULATION LAB Background The Laredal SimManikin system is used for simulation and training for various clinical procedures and exams. Due to the proprietary nature and FDA classification of the device, only the OEM can provide the parts and perform preventative maintenance for this type of equipment. Project Scope The San Francisco VA Medical Center requires repairs and preventative maintenance for one of the simulation mannequins for Simulation Lab. This purchase will ensure the repair and preventative maintenance procedures are completed per the OEM standards for the this equipment. Specifications The OEM will provide the manufacturer recommended parts and services to ensure the machine is restored to operational standards. Delivery Requirements: The Vendor shall notify the Customer POC to plan the delivery date. This notification shall be provided at least one month prior to the vendor-anticipated delivery date. The Vendor shall plan and coordinate with the COR, Biomedical Engineering, and Logistics

Inactive 8(a) Sole Source (FAR 19.8)

PRE-SOLICITATION NOTICE OF INTENT TO SOLE SOURCE Department of Veterans Affairs (VA) Network Contracting Office (NCO 21) intends to award a sole source, firm fixed price contract to Laerdal Medical Co... PRE-SOLICITATION NOTICE OF INTENT TO SOLE SOURCE Department of Veterans Affairs (VA) Network Contracting Office (NCO 21) intends to award a sole source, firm fixed price contract to Laerdal Medical Corporation for upgrades and repairs to a simulation mannequin. The procurement is on behalf of the Department of Veterans Affairs, Veterans Health Administration, Regional Procurement Office West (RPOW), Network Contracting Office (NCO) 21, on behalf of SAN FRANCISCO VA MEDICAL CENTER. The specific items required are as follows: VA’s Gray Market Items terms and conditions apply pursuant to VAAR 852.212-71 Gray Market Items and VAAR 852.212-72 Gray Market and Counterfeit Items. As a result, vendor shall be an OEM, authorized dealer, authorized distributor or authorized reseller for the items identified to be eligible for participation with this acquisition. Vendor must be able to provide the documentation that demonstrates such aforementioned authority. The solicitation for this action will be posted to beta.sam.gov and all responsible sources may submit a capability statement, proposal, or quotation, which shall be considered by the agency. After consideration, the Government will determine whether to proceed with the sole source acquisition. Please keep in mind that patient care and choice in the decision is the highest priority to the VA. The solicitation will be posted on or about February 24, 2022. Please respond to mariah.montalvo@va.gov no later than Wednesday February 24, 2022 at 12:00 pm Pacific time. With your response, please provide evidence showing compliance with the aforementioned Gray Market clauses. Failure to provide the required information may result in a determination that your company is not a viable source. (End of Notice)