ANESTHESIA SET, EPID

The contract is for an epidural anesthesia set featuring a 20-gauge catheter and a 17-gauge Tuohy schliff winged needle, containing 29 components per package, with a unit of issue defined as one package equaling ten sets. Each package must have a shelf life of 12 months, and no more than two months may have elapsed from the date of manufacture to the date of government delivery. Labeling is strictly regulated to include the NSN 6515-01-323-6531, manufacturer name and CAGE code, date of manufacture, expiration or retest date, and contract or lot number, in compliance with Medical Marking Standard No. 1, which supersedes MIL-STD-129 for medical items. Packaging must follow MIL-STD-2073-1E, Level B, utilizing commercial unit containers and shipping containers suitable for safe transport via common carrier, while preservation methods, cleaning, and materials are left to contractor determination. The solicitation, issued by the Defense Logistics Agency under SPE2DS-26-T-086E, requires electronic submission via DIBBS by May 26, 2026, with delivery expected within 20 days after award to the designated APO AE 09094-3219 or Ramstein, Germany address, under FOB destination terms. Technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements, and suppliers must specify the source and part number of the product being offered. The contract incorporates numerous FAR and DFARS clauses related to cybersecurity, trafficking protections, employment verification, hazardous materials, sustainable products, and safeguarding government information, with deviations applied for several provisions under deviation 2026-00038. Electronic invoicing through WAWF is mandatory, and compliance with the Berry Amendment regarding domestic sourcing is required. Although unit pricing for related line items is provided, the total contract value and type are not specified. Offerors must maintain a current SAM registration, provide Unique Entity Identifier and CAGE code if applicable, and represent their size status and socioeconomic categories where relevant. Inspection and acceptance will be conducted by the government at the destination, and all supplies must meet FDA regulations and applicable medical device standards.