TEST KIT, LEGIONELLA

The contract calls for the delivery of one unit of a Legionella urine antigen test kit with a 96-test capacity, identified by NSN 6550014695524 and manufacturer part number 851-000 from Abbott Rapid Dx North America LLC. The item is regulated by the FDA and must be delivered within 20 days of contract award to Fort Bragg, North Carolina, under FOB Destination terms, meaning the contractor bears all transportation costs and risks until delivery. The test kit requires refrigeration between 2 and 8 degrees Celsius at all times and must be shipped within one month of manufacture, with a strict shelf life of six months that is non-extendable. All packaging must comply with Medical Marking Standard No. 1, which supersedes MIL-STD-129, and each container must be clearly marked with the lot number and manufacture date prefixed by “MFD.” Packaging must also adhere to MIL-STD-2073-1E for preservation and protection, using commercial-grade sealed unit containers and robust exterior shipping containers suitable for safe transit via common carrier, including export packaging when necessary. The item is subject to DLA’s Master List of Technical and Quality Requirements and must meet all applicable FDA, OSHA, and DFARS regulations, including hazard communication standards. The contract is structured as a Firm-Fixed-Price agreement and is subject to multiple FAR clauses covering equal opportunity, trafficking in persons, cybersecurity safeguarding, export controls, and prohibited equipment sourcing. Offerors must provide their UEI and CAGE code, represent their small business status, and comply with all electronic submission requirements through the DLA Internet Bid Board System. Inspection and acceptance occur at the delivery point, and invoicing must be processed through WAWF. No unit price is listed in the solicitation, and award is expected to be based on technical acceptability and price in a simplified acquisition process.