Epidural Anesthesia Set Manufacturing

The contract requires the manufacture and supply of complete, sterile, FDA-regulated epidural anesthesia sets comprising 29 individual components, including a 20-gauge catheter and a 17-gauge Tuohy needle with a winged design for secure handling. All sets must be produced under strict sterile conditions and comply with FDA regulations, ensuring they are ready for immediate clinical use without additional preparation. Each set must adhere to a stringent 12-month non-extendable shelf-life requirement, meaning the product must remain sterile, functional, and compliant throughout the entire period without the possibility of extension beyond the stated timeframe. The solicitation is issued as a subcontract under the Department of Defense’s Medical Supply Chain for MD Surg FSF, with a place of performance identified as APO 96260-5479. The NAICS code 325412 indicates the industry is classified under Medical Equipment and Supplies Manufacturing. Responses are due by July 22, 2026, with the solicitation posted on July 16, 2026. All proposals must meet the technical, regulatory, and logistical requirements specified, as failure to comply with any detail—including sterility standards, component specifications, or shelf-life constraints—will result in disqualification. The contract is part of a broader effort to secure reliable, high-quality medical devices for military healthcare operations.