CANNULA, NASAL, OXYGEN

The contract specifies the procurement of nasal oxygen cannulas and microstream capnoline ETCO2 filters for adult, non-intubated use, designed for single-patient application and not manufactured with natural rubber latex. The items are dual-purpose, with the cannula system including a 2-meter filter line and packaged in cases of 25 units each. The equipment is regulated by the FDA, requiring confirmation from a product specialist prior to award. All units must be sealed in commercial-grade, protective packaging that prevents damage during transit and complies with Medical Marking Standard No. 1, which supersedes MIL-STD-129. Packaging must ensure safe, low-cost delivery by common carrier to the designated military destinations in APO, AP and Yokota AB, Japan. The contracting party must provide the manufacturer and part number, with Philips North America LLC identified as the source under part number M2522A. The order quantity is four cases, with a strict delivery window of 20 days from the award date under FOB destination terms and zero variance allowed in quantity. All documentation must adhere to DLA’s technical and quality requirements referenced from the Master List, and special marking and packaging conditions apply as defined in SPE2DS-26-T-195C. The contract is part of a federal procurement under NAICS code 339112, managed by the Department of Defense’s Medical Supply Chain, and requires electronic referral through EBS for FDA-regulated medical items.