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Automated Coagulation Analyzer Supplier

Active
Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This subcontract involves the supply and installation of two fully integrated and automated coagulation analyzers for the 88th Medical Group Clinical Laboratory under the AFLCMC/PZIBA. The required hardware must include integrated CPUs, printers, and peripherals, featuring FDA-approved cutoffs for hemolysis, icterus, and lipemia. Additionally, the equipment must be capable of detecting incorrect fill volumes and sample probe obstructions. The supplier must ensure all equipment holds FDA 510K approval and complies with CLIA 88, CAP, and CLSI standards. The project, managed by the Department of Defense and performed at Wright Patterson AFB, requires the delivery of fully operational and installed analyzers. The response deadline for this opportunity is September 9, 2026.

General Info

Supply and install two FDA-approved automated coagulation analyzers for 88th Medical Group.

Agency

Department Of Defense → FA8601 Aflcmc PzioView Agency

NAICS

334516 - Analytical Laboratory Instrument ManufacturingView NAICS

Place of Performance

Wright Patterson AFB, OH, USA

Set-Aside

NONE

Documents

This scope was carved out of FA860126Q0136.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

Intent to Sole Source Coagulation Analyzer System

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Defense → FA8601 Aflcmc Pzio
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → FA8601 Aflcmc Pzio
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Office AddressN/A
ContactsNo contact information available

Full Description

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Supplies two new, fully integrated, and automated Coagulation analyzers for prime contractors on AFLCMC/PZIBA 88th Medical Group Clinical Laboratory projects. Provides hardware including integrated CPUs, printers, and peripherals with FDA-approved cutoffs for hemolysis, icterus, and lipemia. Equipment must detect sample probe obstructions and incorrect fill volumes. Requires FDA 510K approval and compliance with CLIA '88, CAP, and CLSI standards. Delivers installed and operational analyzers.

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