ATOMIZER, MEDICINAL

The contract is for the procurement of a disposable nasal atomization device with a luer lock connection, designed for consistent and reliable medicinal spray delivery in any position, without a syringe included, and featuring a semipermeable soft plug to absorb runoff while targeting the desired mucosal region. Each unit is individually packaged, and the unit of issue is a box containing 25 devices, identified by NSN 6515-01-486-0832. Delivery is required within 20 days of award to a U.S. Navy facility in San Diego, California, specifically to the Helicopter Sea Combat Wing Pacific, with FOB destination terms placing transportation risk on the contractor. The item must comply with stringent packaging and marking standards, including MIL-STD-2073-1E for packaging and preservation, and Medical Marking Standard No. 1 (MMS No. 1), which supersedes MIL-STD-129 for all medical acquisitions, requiring barcoding and clear labeling. Inspection and acceptance occur at the destination by the government under FAR 52.246-2, and all shipments must be properly sealed and protected. The solicitation, issued under SPE2DS-26-T-295E on August 2, 2026, with responses due August 10, 2026, falls under NAICS code 339112 and is administered by the Department of Defense’s Medical Supply Chain MD Surg FSF. The contract type is unspecified but will be determined by the contracting officer under FAR 52.216-1. Payment must be processed via Wide Area WorkFlow (WAWF), and the contractor must comply with a comprehensive set of FAR and DFARS clauses covering employment equity, trafficking prevention, sustainable products, cybersecurity, subcontracting, inspection, default, and prohibition of toxic materials such as hexavalent chromium. Offerors must provide their Unique Entity Identifier and certify their small business status if claiming socioeconomic preferences, with required representations submitted via SAM.gov. Hazard communication compliance is mandatory under DFARS 252.223-7001, requiring approved labels for hazardous materials. Additionally, the contractor must adhere to DLA packaging requirements RP001 and all applicable regulations governing the transportation and handling of medical devices, with no government identification removed from non-accepted supplies.