REGULATOR, PRESSURE,

The contract specifies the procurement of a medical pressure regulator designed for medical gas administration, classified as a Class I device under FDA Regulation 868.2700. Although a 510(k) submission is not required, compliance with FDA registration, listing, labeling, and good manufacturing practices is mandatory. The item is identified by NSN 6680-01-472-3554 and manufacturer part number RR810-310P2 from FLOTEC INC, with a requirement for three units to be delivered within five days to Travis Air Force Base, California. All packaging must conform to commercial standards as outlined in the procurement document, ensuring each unit is sealed in a container that prevents damage and breakage, and all shipments must use suitable exterior containers that allow safe, cost-effective delivery via common carrier. Mandatory marking follows Medical Marking Standard No. 1, which supersedes MIL-STD-129, and must be applied in accordance with the latest edition available through DLA Troop Support. Delivery is FOB destination with zero variance allowed in quantity, and inspection and acceptance occur at the delivery point. The shipment must use traceable freight methods exclusively—parcel post is prohibited—and must be labeled with the provided government shipping address and internal codes for government use. The contract requires full compliance with DLA packaging requirements and technical specifications, and bidders must clearly state their source and part number to ensure regulatory and logistical alignment.