FDA-Regulated Medical Device Supply

This subcontract involves the supply of FDA-regulated medical devices to prime contractors supporting Department of Defense supply contracts through the Medical Supply Chain MD Surg FSF. The provider is responsible for manufacturing or sourcing devices that strictly adhere to FDA regulations and quality management standards. A critical requirement is ensuring a Type I Code Q shelf-life of 36 months, which must be achieved through the use of FDA-approved manufacturing equipment and specialized packaging. The scope of work focuses on the delivery of physical medical devices to be performed at Fort Bragg. Interested parties must note the response deadline of September 8, 2026, for this opportunity categorized under NAICS code 339113.