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This Government Contract opportunity from Department Of Defense was posted on August 31, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Resuscitation Barrier Device Manufacturing

Closed
Federal

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This subcontract opportunity with the Department of Defense Medical Supply Chain involves the manufacturing of resuscitation barrier devices for prime contractors on DLA supply contracts. The selected provider will produce disposable or reusable barriers featuring integrated pocket-size cases and printed illustrated instructions using medical-grade polymers and specialized printing equipment. To qualify, manufacturers must maintain FDA registration and comply with GMP standards, specifically requiring FDA Regulation 868.5905 Class II and 510(K) Clearance. The contract falls under NAICS code 339113, with a response deadline of September 8, 2026, and performance located in FPO 96692.

General Info

DoD subcontract for FDA-compliant resuscitation barrier device manufacturing, deadline September 8, 2026.

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

FPO, AP, 96692, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-380D.

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

View the prime solicitation

MASK, ORONASAL

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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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Manufactures resuscitation barrier devices for prime contractors on DLA supply contracts. Produces disposable or reusable barriers with integrated pocket-size cases and printed illustrated instructions. Utilizes medical-grade polymers and printing equipment. Requires FDA Regulation 868.5905 Class II, 510(K) Clearance, GMP, and FDA registration. Delivers finished resuscitation barrier devices in pocket-size cases.

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