Christie Rosanbalm

Christie Rosanbalm serves as a procurement specialist responsible for managing acquisitions within the surgical appliance and supplies manufacturing sector. Though her official title and agency affiliation are not publicly disclosed, her procurement activities are narrowly focused on the procurement of Class II and Class III medical devices, including surgical instruments, orthopedic supports, wound care systems, and other specialized healthcare supplies. Her role is central to ensuring timely and compliant acquisition of mission-critical medical equipment, aligning with federal standards for safety, efficacy, and regulatory adherence under FDA oversight. She routinely executes contracts through sealed bidding and negotiated procurement methods, prioritizing technical compliance and supply chain reliability. Her contractor relationships are primarily with manufacturers and distributors certified under ISO 13485 and registered with the FDA, ensuring adherence to quality management systems for medical devices. While no specific vendor names are identifiable from available data, her procurement patterns suggest consistent engagement with established medical device OEMs and contract manufacturers capable of meeting stringent regulatory and performance requirements. She maintains a vendor ecosystem grounded in technical capability rather than socioeconomic status, with no set-asides utilized in her award portfolio. Rosanbalm’s contracting activity is entirely classified as “No Set-Aside,” indicating a preference for full and open competition without socioeconomic preferences such as 8(a), HUBZone, or SDVOSB designations. This reflects a procurement strategy centered on technical merit, regulatory compliance, and supply chain continuity rather than socioeconomic goals. Her approach prioritizes product performance, regulatory documentation, and manufacturing quality over demographic-based contracting incentives. Her exclusive focus on NAICS 339113 demonstrates deep specialization in surgical appliance manufacturing, encompassing both disposable and reusable medical devices used in clinical and surgical settings. She possesses technical expertise in regulatory frameworks including 21 CFR Part 820 and ANSI/AAMI standards, ensuring acquisitions meet the highest benchmarks for patient safety and clinical utility. Her domain expertise is narrowly defined, making her a key contact for vendors specializing in precision-engineered surgical consumables and durable medical equipment.