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Filiform Urethral Device Fabrication

Open
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 fabrication of a specialized Filiform Urethral Device for prime contractors supporting the Department of Defense Medical Supply Chain. The manufacturer is responsible for producing a 3FR, 12-inch nominal straight device by integrating a Dacron tube with biocompatible metal components to create a specific olive tip geometry. Production requires the use of precision extrusion or molding equipment and strict adherence to FDA Regulation 876.5130 Class II standards to ensure the delivery of a finished, sterilizable medical device. The project is managed under NAICS code 339113 and is associated with the Medical Supply Chain MD Surg FSF. Performance of the contract is designated for Fort Stewart, Georgia. Interested parties should note the response deadline of November 18, 2026, for this specialized medical device procurement.

General Info

Fabricate FDA Class II Filiform Urethral Devices for DoD medical supply by November 2026.

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

FORT STEWART, GA, 31314-5185, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-27-T-1808.

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

View the prime solicitation

FILIFORM, URETHRAL

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Timeline

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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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Manufactures a specialized medical device for prime contractors on DLA Troop Support Medical Supply Chain projects. Fabricates a 3FR, 12-inch nominal straight device by integrating a Dacron tube with biocompatible metal components to form an olive tip geometry. Requires precision extrusion or molding equipment and compliance with FDA Regulation 876.5130 Class II. Delivers one finished, sterilizable Filiform Urethral Device.

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