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Auto-Injector Device Fabrication

Active
Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This subcontract through DLA Troop Support involves the fabrication and supply of mechanical auto-injector delivery hardware for prime contractors supporting Department of Defense medical device contracts. The scope of work focuses on the production of unfilled devices, specifically the fabrication of outer casings, safety caps, and spring-loaded injection mechanisms utilizing medical-grade polymers and precision plastic molding. A primary requirement of the contract is ensuring the stability of the container and closure system in accordance with the statement of work. To qualify for this engagement, the provider must maintain FDA medical device registration and adhere strictly to current Good Manufacturing Practice compliance. The opportunity is categorized under NAICS code 339112, with a response deadline set for November 2, 2026.

General Info

Fabricate mechanical auto-injector hardware for DoD via DLA Troop Support by November 2026.

NAICS

339112 - Surgical and Medical Instrument Manufacturing

Place of Performance

PA

Set-Aside

NONE

Documents

This scope was carved out of SPE2D2-26-R-0009.

The full solicitation package (3 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

PHARM MANUF/DISTR DIV - FSA

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Timeline

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Response Deadline

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Response Deadline

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Organization & Contact Information

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AgencyDepartment Of Defense → DLA Troop Support
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Supplies mechanical auto-injector delivery hardware for prime contractors on DoD medical device contracts. Fabricates spring-loaded injection mechanisms, outer casings, and safety caps using precision plastic molding and medical-grade polymers. Ensures container/closure system stability per SOW. Requires FDA medical device registration and cGMP compliance. Delivers unfilled auto-injector devices.

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