CAUTERY, BATTERY OPERATED

A battery-operated cauterization device with a U-tip, designed for single-use and sterile application, operates at a temperature of 2200 degrees Fahrenheit and is supplied in packages of ten, complete with case and batteries. The item has a mandatory 48-month shelf life with no extensions permitted, and no more than seven months may have passed from the date of manufacture to delivery to the government. The product is regulated by the FDA, requiring a referral to the product specialist for confirmation prior to award, including full details of the bidder, manufacturer, part number, and item description. Packaging must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and all units must be sealed in commercial-grade containers that protect against damage and ensure safe delivery via common carrier at the lowest possible cost. The unit of issue is a pack of ten, with a total quantity of three packs required under purchase request 7017460775, to be delivered FOB destination within 20 days of contract award. The device is manufactured by Bovie Medical Corporation under part number AA03 and distributed by Cardinal Health 200, LLC. Technical and quality requirements are governed by the DLA Master List, and all markings, packaging, and handling must adhere strictly to DLA specifications for medical acquisitions, including commercial packaging standards and proper labeling procedures.