6525--673B50076, UPGRADE, LFO, FUJIFILM HEALTHCARE, XR MRI VISN 8, TAMPA, FL, $762,121.54, DD 05/30/26
Overview
Buyer
Place of Performance
NAICS
PSC
Set Aside
Original Source
Timeline
Qualification Details
Fit reasons
- NAICS alignment with historical contract wins in similar service areas.
- Scope strongly matches core technical capabilities and delivery model.
Risks
- Past performance thresholds may require one additional teaming partner.
- Potential clarification needed on staffing minimums before bid/no-bid.
Next steps
Validate eligibility requirements, assign capture owner, and schedule partner outreach to confirm teaming strategy before submission planning.
Quick Summary
The Department of Veterans Affairs (VA), specifically the NAC High Tech Orders office, has awarded a sole-source delivery order to Fujifilm Healthcare Americas Corporation for the upgrade of an existing Fuji Oasis MRI system at a VA VISN 8 facility in Tampa, FL. The award, valued at $762,121.54, was made on February 4, 2026.
Scope of Work
This delivery order covers the comprehensive upgrade of an existing Fuji Oasis MRI system. The scope includes all associated computer hardware, software, and MRI components necessary to modernize the system. This ensures continued operational capability and compliance for the medical imaging equipment.
Contract & Timeline
- Contract Type: Sole-Source Delivery Order (Logical Follow-On)
- Award Number: Related to IDIQ Contract No. VA797H-17-D-0020 (Delivery Order No. 673B50076)
- Awardee: Fujifilm Healthcare Americas Corporation
- Award Amount: $762,121.54
- Award Date: February 4, 2026
- Published Date: February 5, 2026
- Set-Aside: Not applicable; this was a sole-source action.
Evaluation & Justification
This action was justified as a logical follow-on to an existing IDIQ contract, citing an exception to fair opportunity. Fujifilm Healthcare was identified as the only contractor capable of providing the required upgrade due to their proprietary knowledge of the existing system's hardware and software, and its specific FDA 510K medical device certification. The contracting officer determined the anticipated cost to be fair and reasonable.
Additional Notes
This award is for a specific upgrade. Future requirements for similar services will be handled on a case-by-case basis, with attempts to provide fair opportunity to all schedule holders where feasible. The technical requirements were reviewed and certified by the facility's Biomedical Engineer and clinical end user.