Medical Device Manufacturing & Supply (GC Cavity Conditioner)

The contract requires the manufacture, packaging, labeling, and delivery of 6gm units of GC Cavity Conditioner, an FDA Class II medical device, strictly adhering to Department of Defense technical specifications, shelf-life standards, and military packaging requirements. All production must ensure full compliance with regulatory and operational mandates for use in military medical applications, with quality control measures embedded throughout every stage of the process. The product must meet exacting durability and sterilization criteria suitable for storage and deployment in field conditions. Performance is to be carried out at or from Suffolk, Virginia, with a response deadline of August 10, 2026, and the contract is solicited as a subcontract under NAICS code 339114, which classifies it within the medical appliance and equipment manufacturing sector. The awarding agency is the Department of Defense through the Medical Supply Chain FSH, and delivery must align with military logistics protocols for timely, secure, and traceable distribution to designated endpoints. All units must be labeled and packaged to sustain integrity over the designated shelf life under expected environmental conditions without degradation or contamination.