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This Government Contract opportunity from Department Of Defense was posted on September 17, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Supply of Arterial Pressure Monitoring Cables

Closed
Federal

Contract Overview

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This subcontract involves the supply of arterial pressure monitoring cables for prime contractors under DLA Troop Support medical supply contracts. The required equipment must meet the specifications for NSN 6515-01-434-6106 and ICU Medical Sales, Inc. part number 42661-04. Each unit must be delivered as a completed, packaged monitoring set in a sealed container to ensure protection against damage. The contract is managed by the Department of Defense under the Medical Supply Chain MD Surg FSF, with performance taking place at FPO 09583. To be eligible, providers must maintain an active SAM registration and ensure full compliance with FDA regulations for medical devices. The response deadline for this opportunity is September 23, 2026.

General Info

Supply arterial pressure monitoring cables for DLA Troop Support by September 23, 2026.

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers

Place of Performance

FPO, AE, 09583, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-450H.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

CABLE, MONITORING SET, A

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Supplies arterial pressure monitoring cables for prime contractors on DLA Troop Support medical supply contracts. Provides NSN 6515-01-434-6106 matching ICU Medical Sales, Inc. P/N 42661-04 specifications. Packs each unit in a sealed container to prevent damage. Requires FDA regulation compliance for medical devices and active SAM registration. Delivers the completed, packaged monitoring set.

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