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This Government Contract opportunity from Department Of Defense was posted on September 9, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Medical Disposable Component Supplier

Closed
Federal

Contract Overview

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This subcontract opportunity with the Department of Defense, specifically the Medical Supply Chain MD Surg FSF, seeks a supplier to provide individual medical components for prime contractors fulfilling DLA supply contracts. The scope involves the manufacture or distribution of sterile medical disposables, such as bulb syringes, umbilical cord clamps, and disposable scalpels, delivered in bulk quantities for integration into larger medical kits. Eligible providers must maintain FDA approval or registration for medical devices and hold valid sterilization certifications. The contract falls under NAICS code 339113 and is designated for performance at FPO 09566-4008. Interested parties must respond by September 14, 2026.

General Info

DoD seeks FDA-approved suppliers for sterile medical components by September 14, 2026.

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

FPO, AE, 09566-4008, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-411G.

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

View the prime solicitation

DELIVERY KIT, OBSTETRIC

AI Contract Breakdown

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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 individual medical components for prime contractors delivering DLA supply contracts. Manufactures or distributes sterile medical disposables, including disposable scalpels, umbilical cord clamps, and bulb syringes, in bulk quantities for integration into larger delivery kits. Requires FDA approval/registration for medical devices and sterilization certifications. Delivers bulk quantities of individual medical components.

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