Sterile Medical Device Packaging and Labeling

The contract entails the design, validation, and production of sterile barrier systems for medical devices, encompassing pouches, trays, and labeling solutions that meet stringent regulatory standards for shipping and handling. These systems must ensure the integrity and sterility of medical devices throughout their distribution lifecycle, adhering to industry-specific requirements for contamination control, material compatibility, and performance under environmental stress. The work is classified under NAICS code 326199, indicating non-metallic mineral product manufacturing, and is structured as a subcontract under the Department of Veterans Affairs’ 261-NETWORK Contract Office 21, with performance expected to support federal medical supply chains. The solicitation was posted on August 8, 2026, and is open for competitive bidding by qualified subcontractors capable of meeting technical and compliance benchmarks for medical-grade packaging. While no set-aside classification or geographic performance restrictions are specified, the packaging solutions must align with U.S. medical device regulations and maintain consistent quality across high-volume production. This contract supports critical healthcare logistics for the Veterans Affairs system, requiring proven expertise in sterile packaging validation, regulatory documentation, and scalable manufacturing processes capable of delivering reliable, compliant systems under tight operational timelines.