DRAINAGE UNIT, PLEURAL CAVITY

The contract specifies the procurement of a Mobile Chest Drain, Waterless Setup, with a 500ml collection capacity, one-way valve, simple air leak detection, compact and lightweight design, capable of suction or gravity drainage, delivered in cases of six units each, identified by NSN 6515-01-525-4904. The item is a Type I (Code Q) medical device with a non-extendable shelf life of 36 months, and delivery to the Government must occur no more than five months after the manufacturer’s date. All units must be sealed in commercial packaging designed to prevent damage, packed in commercial shipping containers suitable for safe transport at the lowest rate, and marked in accordance with Medical Marking Standard No. 1, which replaces MIL-STD-129. Labels must include the manufacturer date, expiration or retest date, and contract or lot number. The product must meet FDA Regulation 880.6740, Class II, including registration, listing, labeling, and GMP requirements, though a 510(k) is not required. The delivery point is APO AE 09227-0000 with a secondary freight address in Kaiserslautern, Germany, under FOB Destination terms, and shipment must comply with DLA’s packaging and transportation standards including the use of WAWF for payment and receiving reports. The contract incorporates the DLA Master Solicitation Revision 105 and requires compliance with numerous DFARS and FAR clauses covering cyber security, safeguarding controlled information, prohibition of certain foreign-sourced materials, whistleblower protections, anti-trafficking, equal opportunity, and hazardous substance handling. The offeror must represent compliance with the Buy American Act and Berry Amendment, and ensure no covered defense telecommunications equipment or services are provided. All bids must be submitted through DIBBS by August 17, 2026, and the successful vendor must register with DLA’s AMPS system to access the Vendor Shipment Module within two months of award.