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This Government Contract opportunity from Department Of Defense was posted on September 9, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Supply of Safety Hypodermic Syringes and Needles (10ML 21 Gage)

Closed
Federal

Contract Overview

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This subcontract involves the supply of 10ML 21 Gage safety hypodermic syringes and needles for prime contractors supporting Department of Defense medical supply contracts. The products must be delivered in packages of 100, adhere to Medical Marking Standard No. 1, and maintain a non-extendable shelf-life of 60 months. Performance for this contract is located at Camp Pendleton. Compliance with FDA Regulation 880.5860 Class II is mandatory, requiring full registration, listing, labeling, and adherence to Good Manufacturing Practices, along with a 510(k) premarket notification. The contract falls under NAICS code 423450 and is managed by the Medical Supply Chain MD Surg FSF agency.

General Info

Supply 10ML safety syringes to Camp Pendleton per FDA and DoD medical standards.

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers

Place of Performance

CAMP PENDLETON, CA, 92055-5627, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-412P.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

SYRINGE AND NEEDLE, HYPODERMIC, SAFETY

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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 safety hypodermic syringes and needles for prime contractors delivering DLA medical supply contracts. Provides 10ML 21 Gage syringes in packages of 100, adhering to Medical Marking Standard No. 1 and maintaining a 60-month non-extendable shelf-life. Requires compliance with FDA Regulation 880.5860 Class II, including Registration, Listing, Labeling, GMPs, and a 510(k) premarket notification. Delivers the physical medical devices.

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