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Medical Device Supplier – Temporary Pelvic Stabilization Device

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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A subcontract has been issued for the supply of a green, manually cuttable pelvic stabilization device featuring Velcro and shoelace fasteners, designed to meet FDA and DLA compliance standards. The device is intended for temporary use in medical emergencies and must adhere to strict regulatory requirements for safety and performance. The contract is associated with the Department of Defense’s Medical Supply Chain under the agency name MEDICAL SUPPLY CHAIN MD SURG FSF, with performance specified to occur in San Antonio, Texas, at ZIP code 78226. The solicitation was posted on August 2, 2026, and responses are due by August 10, 2026, with the NAICS code 33999A indicating classification under Other Miscellaneous Medical and Dental Equipment Manufacturing. The procurement is managed through the DIBBS platform with the reference number SPE2DS26T294E.

General Info

Green, manually cuttable pelvic stabilization device with Velcro and shoelace fasteners for emergency medical use.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

NAICS

33999AView NAICS

Place of Performance

SAN ANTONIO, TX, 78226, US

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

PostedAug 2

subcontract

Response DeadlineAug 10

Submission deadline

Response Deadline

08/10/2026, 05:00:00 PM UTCin 2 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 a green, manually cuttable pelvic stabilization device with Velcro and shoelace fasteners compliant with FDA and DLA standards.

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