DOPPLER, FETAL HEART RATE

The contract pertains to the procurement of a fetal heart rate Doppler device regulated by the FDA under Class II requirements, requiring compliance with marketing regulations including registration, listing, labeling, and good manufacturing practices, regardless of whether a 510(k) submission is needed. The item is identified by NSN 6515-01-713-8347 and manufacturer part number L250-SD3 from CooperSurgical Inc, with a single unit quantity and a delivery deadline of 20 days from the award date, to be delivered FOB destination to Cannon AFB, New Mexico. Packaging must comply with commercial standards as specified in the procurement document, ensuring each unit is sealed in a container that protects against damage and breakage, and all units must be packed in commercial shipping containers suitable for safe, cost-effective delivery via common carriers. Medical marking must adhere to Medical Marking Standard No. 1, which supersedes MIL-STD-129, and copies are available through DLA Troop Support or the official DLA website. Palletization must follow DLA Packaging Requirements for Procurement, and shipment must be made via traceable means—parcel post is prohibited. Technical and quality requirements referenced in the DLA Master List apply, with the applicable revision determined by the solicitation date for simplified acquisitions. The contract includes detailed delivery instructions, government-use markings, and a designated point of contact for inquiries.