Opportunities / HEALTH AND HUMAN SERVICES, DEPARTMENT OF

Notice of Intent to Sole Source – Philips North America

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Notice typeSpecial Notice
Solicitation #27-000177
DepartmentHEALTH AND HUMAN SERVICES, DEPARTMENT OF
Sub-tier / officeNATIONAL INSTITUTES OF HEALTH / NATIONAL INSTITUTES OF HEALTH - CC
NAICS339112 — Surgical and Medical Instrument Manufacturing
PSC6515
Set-asideNo set-aside
PostedNov 2, 2026
Response deadlineNov 23, 2026 (2026-11-23T17:00:00-05:00)
Place of performanceMD, 20892
Primary contactKristin Nagashima · kristin.nagashima@nih.gov
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Description (excerpt)

This acquisition is for three (3) Philips Cardiac Workstation 7000 units, compatible trolleys, and implementation services for patient care at the National Institutes of Health (NIH) Clinical Center (CC) Department of Clinical Research Informatics (DCRI). • Product Service Code: 6515 – Medical Instruments, Equipment, and Supplies • NAICS Code: 339112 – Surgical and Medical Instrument Manufacturing • Place of Performance: Bethesda, MD 20892 USA POTS: 27-000177 Description: This is a notice of intent, not a request for a quotation. A solicitation document will not be issued and quotations will not be requested. The National Institutes of Health (NIH) intends to award a fixed price purchase order to Philips North America, located at 222 Jacobs St, East Cambridge, MA, on a firm fixed price sole source award basis to provide three (3) Philips Cardiac Workstation 7000 units, compatible trolleys, and implementation services for patient care at the National Institutes of Health (NIH) Clinical Center (CC) Department of Clinical Research Informatics (DCRI). The Clinical Center’s requirement is driven by interoperability with its existing EKG-to-CRIS environment. The SOW states that the Philips model can be added to the existing CRIS interfaces, enabling electronic orders/results and an automated workflow in which authorized staff can review, annotate, and sign EKG reports online for automatic upload to CRIS. The SOW further states that this automation is intended to reduce errors, keep reports digital, improve availability, and improve patient safety. A different manufacturer’s product that requires development of an additional interface would not meet the requirement as presently defined because it would add interface development, validation, implementation, and operational risk outside the intended scope. Accordingly, the unique qualification is native/established compatibility with the existing Philips-to-CRIS interface and workflow, not merely the manufacturer’s trade name. This acquisition is being conducted using policies unique to the Federal Acquisition Regulation (FAR) Part 13 – Simplified Acquisition Procedures, Subpart 13.106-1(b)(1), For purchases not exceeding the simplified acquisition threshold (SAT), contracting officers may solicit from one source if the contracting officer determines that the circumstance of the contract action deem only one source reasonably available. Contracts awarded using FAR Part 13-Simplified Acquisition Procedures are exemp …

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