Domestic Origin Certification & Representation

The contract requires the submission of certification and documentation to verify the domestic origin of an oxygen minilator, ensuring full compliance with the Buy American Act and FAR 52.219-28 provisions. This obligation centers on demonstrating that the product is manufactured in the United States using domestic components and materials, aligning with federal procurement integrity standards. The submission must conclusively establish country of origin without ambiguity, as failure to meet these requirements may result in disqualification or contract non-compliance. The solicitation is issued under NAICS code 541840, categorized as a subcontract, and is managed by the Department of Defense through the Medical Supply Chain MD Surg FSF office. The response deadline is set for July 20, 2026, with the opportunity posted on July 12, 2026, providing a limited eight-day window for submission. All documentation must be submitted via the designated DIBBS platform, and there is no set-aside designation or specific small business preference indicated. The place of performance and point of contact details are unspecified, suggesting that the obligation is purely documentation-driven rather than requiring physical delivery or on-site services.