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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.

Supply of FDA-Regulated Medical Device (0.30MM 60MM)

Closed
Federal

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This subcontract involves the supply of FDA-regulated medical devices measuring 0.30MM by 60MM to prime contractors for the Department of Defense via the Medical Supply Chain MD Surg FSF. The provider is responsible for manufacturing or sourcing these devices in cases of 1,000 units, ensuring all products and packaging adhere to FDA regulations, DLA RP001 specifications, and the DLA Master List of Technical and Quality Requirements RA001. To be eligible, the contractor must maintain valid FDA registration and certification. The contract requires the delivery of packaged and labeled cases to the designated place of performance in FPO 96632. This opportunity falls under NAICS code 339113, with a response deadline of September 8, 2026.

General Info

Supply FDA-regulated medical devices to DoD via Medical Supply Chain by September 2026.

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

FPO, AP, 96632, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-384W.

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

View the prime solicitation

NEEDLE, ACUPUNCTURE

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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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Supplies FDA-regulated medical devices (0.30MM 60MM) for prime contractors on DLA supply contracts. Manufactures or sources devices in cases of 1,000 units per FDA regulations and DLA Master List of Technical and Quality Requirements (RA001). Utilizes medical-grade materials and packaging meeting DLA RP001 specifications. Requires FDA registration and certification. Delivers packaged and labeled cases of 1,000 units.

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