DISTILLED WATER, REA

Distilled Water, Reagent, specified under NSN 6550-01-310-1677, is procured for in vitro diagnostic use only and must not be used for infusion, injection, or irrigation. The product is packaged in units of PG, with each unit consisting of four one-gallon containers. All packaging must comply with commercial standards as defined in the procurement document, requiring each unit to be sealed in a container that protects against damage or breakage, and shipped in suitable exterior containers that ensure safe delivery via common carrier at the lowest possible rate to the designated delivery point in APO, AP 96260-5479, or via freight to Camp Carroll, Korea. Labeling and marking must follow Medical Marking Standard No. 1 (MMS No. 1), which supersedes MIL-STD-129, and must include the date of manufacture, expiration or retest date, and contract or lot number, all in accordance with the latest revision of MMS1C. The product must have a non-extendable shelf life of 12 months, with no more than one month elapsed between the date of manufacture and delivery to the government, and must be stored at room temperature. Technical and quality requirements referenced by R or I numbers are governed by the DLA Master List of Technical and Quality Requirements, with the revision in effect on the award date controlling compliance. The solicitation, issued under SPE2DS-26-T-111M, falls under NAICS code 621410 and is not set aside for small businesses. Offers are due by June 8, 2026, with deliveries required 84 days after receipt of order, delivered FOB destination. The contract incorporates numerous FAR and DFARS clauses, including requirements for System for Award Management registration, cybersecurity compliance under NIST SP 800-171, safeguarding covered defense information, prohibition on covered defense telecommunications equipment, and compliance with the Buy American Act and Berry Amendment. Contractors must use Wide Area Workflow for invoicing and ensure receiving reports meet DFARS Appendix F standards. Offerors must be registered in SAM, provide unique entity identifiers, and comply with representations regarding small business status, economic disadvantage, and prohibited practices including human trafficking and forced labor. All materials are subject to FDA regulation, and alternate product submissions require full technical documentation. The procurement is subject to deviation 2026-00