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SolicitationsHEALTH AND HUMAN SERVICES, DEPARTMENT OFNAICS 811210

Fibroscan Annual Service Contract

HEALTH AND HUMAN SERVICES, DEPARTMENT OF · Solicitation 75N98026Q00802 · NAICS 811210 · 8(a) Sole Source · Closed

Solicitation details

Solicitation number75N98026Q00802
Notice ID25ac6b2076fe4e5e8baa8f6234dea5e6
AgencyHEALTH AND HUMAN SERVICES, DEPARTMENT OF
Sub-tierNATIONAL INSTITUTES OF HEALTH
Contracting officeNATIONAL INSTITUTES OF HEALTH OLAO
NAICS code811210
Product / service code (PSC)J066
Set-aside8(a) Sole Source
Notice typeCombined Synopsis/Solicitation
Posted15 July 2026
Response deadline25 July 2026 (closed)
Place of performanceBethesda, MD, USA
CompetitionCompetitive

Description

The requirement is for a service agreement to support the FibroScan 430 Mini+ Package currently in operation at the National Institutes of Health Clinical Center. The instrument is used to measure liver stiffness for both clinical patient care through the hepatology consult service and for clinical research conducted by the Liver Diseases Branch, as well as collaborative studies with the Diabetes, Endocrinology, and Obesity Branch and other Institute Centers. The service agreement is required to ensure continued operation, proper calibration, and reliable performance of the existing FibroScan 430 Mini+ system. No other vendor can be used to meet this requirement, as maintenance, calibration, and repair must be performed in accordance with the manufacturer s specifications to ensure the accuracy and reliability of the instrument. The FibroScan 430 Mini+ utilizes vibration-controlled transient elastography, and proper probe calibration is required to maintain measurement accuracy. Services performed outside of the required specifications would risk producing invalid or inconsistent results. Alternative service providers are not feasible, as maintenance and calibration of this specialized equipment require proprietary knowledge, tools, and procedures specific to the FibroScan system. The use of non-authorized service providers could result in improper calibration, equipment malfunction, or loss of data integrity, which would compromise both clinical care and ongoing research protocols.

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