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Urethral Catheter Supply (Medical Device Manufacturing)

Active

Federal

Response Deadline08/10/2026, 05:00:00 PM UTC

Contract Overview

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

AI Contract Overview

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The contract pertains to the supply of sterile urethral catheters identified by NSN 6515010983623, packaged in sealed unit containers that meet all applicable DLA and federal medical device standards. The items must be manufactured in compliance with stringent quality and safety regulations to ensure suitability for military medical use, with performance fulfillment required at Fort Lewis, WA, under the 98433-9500 zip code. This is a subcontract action under NAICS code 325620, which classifies the industry as medical equipment and supplies manufacturing, and is managed by the Department of Defense through the Medical Supply Chain MD Surg FSF organization. Interested parties must submit responses by the deadline of August 10, 2026, with the solicitation active as of August 2, 2026, and available for review at the designated DIBBS portal.

General Info

Supply of sterile urethral catheters to Fort Lewis, WA, per DLA and federal standards, bid due August 10, 2026.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

NAICS

325620 - Toilet Preparation ManufacturingView NAICS

Place of Performance

FORT LEWIS, WA, 98433-9500, US

Set-Aside

NONE

Documents

(0)

No documents available

AI Contract Breakdown

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Timeline

PostedAug 2

subcontract

Response DeadlineAug 10

Submission deadline

Response Deadline

08/10/2026, 05:00:00 PM UTCin 7 days

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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

Organization / Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

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Office AddressN/A

ContactsNo contact information available

Full Description

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Supply of sterile urethral catheters (NSN: 6515010983623) in sealed unit containers compliant with DLA and federal medical device standards.

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