Medical Kit Assembly & Sterile Packaging of Wound Closure Kits

The contract requires the manufacture and sterile assembly of facial laceration trays designed for immediate use in trauma and surgical settings, with all components packaged in disposable, tamper-evident materials that meet stringent medical and regulatory standards. Each kit must be certified to maintain sterility and integrity for a minimum of 36 months from the date of packaging, ensuring long-term usability in both clinical and field environments. The assembly process must comply with current Good Manufacturing Practices and include rigorous quality control checkpoints to guarantee consistent performance and patient safety. The work is to be performed at a facility capable of supporting sterile processing and medical device assembly, with the place of performance specified as Fort Bragg, North Carolina, 28310. This is a subcontract opportunity under the NAICS code 325620 for Medical Equipment and Supplies Manufacturing, issued by the Department of Defense through its Medical Supply Chain division. Interested parties must submit responses by August 3, 2026, and the solicitation is accessible via the DIBBS platform. Failure to meet sterility, shelf-life, or packaging requirements will result in rejection, and all deliverables must align with applicable FDA and ISO standards for reusable and disposable medical devices.