Sterile Medical Device Manufacturing and Packaging

The contract mandates the manufacture and sterile packaging of 30mL laboratory syringes featuring Luer Lock connections, with each pack containing three units, all produced to meet a 60-month shelf life requirement and full compliance with federal labeling standards. The work must be executed in accordance with stringent medical device manufacturing protocols to ensure sterility, functionality, and regulatory conformity throughout the product lifecycle. The syringes are intended for laboratory use within the Department of Defense’s medical supply chain and must adhere to the highest quality and safety benchmarks applicable to sterile medical devices. The solicitation, issued under NAICS code 339113 for Medical Equipment and Supplies Manufacturing, is structured as a subcontract with a response deadline of July 20, 2026. The place of performance is designated as Sandston, Virginia, with a zip code of 23150-5050, indicating that production and packaging activities must occur at or be coordinated through this location. The contracting entity is the Department of Defense through its Medical Supply Chain FSH office, and proposals must be submitted via the DIBBS portal to meet procurement requirements and timelines. Compliance with all federal regulations, including labeling, packaging, and shelf life validation, is mandatory and non-negotiable for award consideration.