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This Government Contract opportunity from Department Of Defense was posted on September 28, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Full Body Infant Restraint Board Supply

Closed
Federal

Contract Overview

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This subcontract involves the manufacture and supply of infant full-body restraint boards for prime contractors supporting Department of Defense DLA Troop Support Medical Supply Chain projects. The provider is responsible for sourcing or producing boards that strictly adhere to NSN 6530-01-533-7556 and FDA Regulation 880.6760 Class I standards. All units must feature markings compliant with Medical Marking Standard No. 1 and meet the specific requirements outlined in DLA RA001 and RP001. To qualify, the supplier must maintain active FDA registration and ensure Good Manufacturing Practice compliance for Class I medical devices. The contract specifies that all completed restraint boards are to be delivered FOB Destination to the designated place of performance. This procurement falls under NAICS code 339113 and is managed through the Medical Supply Chain FSH agency.

General Info

Manufacture and supply FDA-compliant infant restraint boards for DoD DLA medical projects.

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 SPE2DH-26-T-7165.

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

View the prime solicitation

RESTRAINT BOARD, FULL B

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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 CHAIIN FSH
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Supplies infant full-body restraint boards for prime contractors on DLA Troop Support Medical Supply Chain projects. Manufactures or sources boards meeting NSN 6530-01-533-7556 and FDA Regulation 880.6760 Class I. Applies markings per Medical Marking Standard No. 1 and adheres to DLA RA001 and RP001 requirements. Requires FDA registration and GMP compliance for Class I devices. Delivers completed restraint boards FOB Destination.

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Keith Deutsch
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