PRESSURE MONITOR KIT

The Pressure Monitor Kit is a sterile medical device package containing a diaphragm chamber, 18-inch needle, 2.5-inch gauge, side-port component, and a 3 mL syringe pre-filled with 0.9% sodium chloride injection, USP, with a detachable plunger, designed for use with intra-compartmental pressure monitoring sets and pulsed irrigation pumps. The item is identified by NSN 6515-01-334-3233 and is subject to FDA regulation, requiring a 510(k) submission, registration and listing, labeling compliance, and adherence to current good manufacturing practices. Each unit must have a non-extendable shelf life of 24 months, and no more than three months may elapse between the date of manufacture and delivery to the government. The unit of issue is a package containing six kits, and all packaging must meet commercial standards as specified in the procurement document, with each kit sealed in a protective container and shipped in suitable commercial exterior containers ensuring safe delivery at the lowest cost to the point of delivery in APO, ZIP 09461-9997, with freight address in the United Kingdom. Marking must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and include the NSN, manufacturer and CAGE code, date of manufacture, expiration date, and contract or lot number. The supply is governed by a solicitation issued by DLA Troop Support under number SPE2DS-26-T-212V with a response deadline of July 16, 2026, and a required delivery within five days of award. The procurement uses simplified acquisition procedures and may be automatically awarded with preference given to HUBZone concerns. All contractors must be registered in the System for Award Management and comply with DFARS and FAR clauses addressing cybersecurity, safeguards for covered defense information, whistleblower rights, contractor reporting obligations, and prohibitions on covered telecommunications equipment. Invoicing must be processed electronically through WAWF, with documentation types required per fixed-price or cost-type line item structure. The kit components are intended for surgical use in combat and field medical environments, and the contractor assumes full liability for safety, compliance with hazard communication standards, and adherence to all federal, state, and local regulations regarding hazardous materials. The solicitation is unrestricted with no set-aside and follows the DLA Master Solicitation for Automated Simplified Acquisitions