AIRWAY, NASOPHARYNGE

The contract calls for the procurement of 8 packages, each containing 10 sterile, disposable nasopharyngeal airways, 28 French, made of plastic and intended for medical use under NSN 6515-01-129-5437. Delivery is required within 20 days of award to Brooksville, Florida, with FOB Destination terms placing full transportation responsibility and risk on the supplier until receipt at the designated location. The product must maintain a minimum 60-month shelf life, with no more than nine months having passed between the date of manufacture and delivery, and all packaging must be clearly marked with the lot number and manufacture date prefixed by “MFD.” Packaging and marking must adhere to MIL-STD-129 and DLA’s Medical Marking Standard No. 1, while also complying with ASTM D3951 and DLA’s RP001 packaging requirements. Bar-coding is mandated for traceability, and hazardous materials must be labeled according to 29 CFR 1910.1200. The contract is a simplified acquisition under solicitation SPE2DS-26-T-097P, with responses due by June 1, 2026, through the DIBBS portal. The contracting activity is under the Department of Defense’s Medical Supply Chain, and award is likely to be made on a fixed-price basis using a Lowest Price Technically Acceptable methodology, though not explicitly confirmed. All suppliers must register in SAM, provide a Unique Entity Identifier and CAGE code, and disclose any socioeconomic status claims such as small business, HUBZone, SDVOSB, or WOSB eligibility. Compliance with FAR and DFARS clauses is required, including those addressing equal opportunity, human trafficking, employment verification, sustainable products, hazardous material identification, authorization and consent, whistleblower rights, data disclosure, supply chain integrity, and NIST SP 800-171 cybersecurity requirements. Invoices must be submitted via WAWF, and the government reserves the right to inspect and accept goods at the delivery point. The contractor must also ensure compliance with all applicable FDA regulations for Class I medical devices and remove any government identification from rejected items as per RQ011. Financial details are not specified in the solicitation, and the total contract value cannot be determined due to missing unit pricing in the CLIN table.