Sterile Vascular Shunt Manufacturing and Packaging

The contract calls for the manufacture of sterile, single-use vascular shunts to exact dimensional specifications, ensuring strict compliance with FDA regulations for medical devices. Packaging must adhere to MIL-STD-2073-1E standards for preservation and packaging of military equipment, while marking requirements follow MIL-STD-129 for uniform labeling and identification. All products must be produced in a controlled, sterile environment to maintain integrity and safety for clinical use. The manufacturing and packaging processes are subject to stringent quality control and documentation protocols to ensure consistent compliance with federal and military standards. The solicitation is issued as a subcontract under the Department of Defense’s Medical Supply Chain, specifically managed by the MD SURG FSF office, with performance required at Fort Bliss, Texas, 79916-2527. The opportunity was posted on July 23, 2026, and responses are due by July 29, 2026, indicating a tight turnaround for qualified manufacturers. The NAICS code 339112 identifies this as a medical device manufacturing effort, targeting vendors with experience in sterile, precision medical components. The procurement is part of a broader effort to secure reliable, compliant supply lines for critical surgical equipment within military medical operations.