Medical Device Manufacturing – Sterile Urethral Catheters

The contract requires the manufacture of sterile 20FR red Robinson urethral catheters to meet stringent regulatory standards set by the FDA and the Defense Logistics Agency, with full compliance to established shelf-life requirements. All products must be produced under rigorous quality control protocols to ensure clinical safety and performance, accompanied by comprehensive regulatory documentation to support approval and traceability. The manufacturing facility must maintain compliance with FDA regulations and DLA specifications throughout production, packaging, labeling, and storage to guarantee the integrity of each unit delivered. This is a subcontract solicitation under NAICS code 325620, issued by the Department of Defense through the Medical Supply Chain MD SURG FSF office, with performance required at Fort Bragg, North Carolina, zip code 28310. The solicitation was posted on July 21, 2026, and responses are due by July 27, 2026, indicating a short, high-priority procurement window. All submissions must align with the government’s expectations for sterile medical device production, including documentation of sterilization validation, material sourcing, and ongoing quality assurance practices. The contract emphasizes full accountability in meeting defense medical supply needs with precision and reliability.