UNSPSC 42281811: Sterilization container locks

In this classification, this commodity indicates a product that is used as a container lock associated with the sterilization process in a medical setting. US FDA regulates Sterilization container locks under 21 CFR 880.6850 and under FDA product code KCT. Most nations, for tariff and trade purposes, schedule these products under HS 901811.

UNSPSC 42281811 Sterilization container locks, a Commodity code, covers sterilization and autoclave service, maintenance, and equipment procurement for state and local health, laboratory, and administrative facilities. Recent state and local solicitations under this code show demand for both OEM replacement parts, accessories, and service contracts for laboratory sterilization equipment including autoclaves and biosafety cabinets. The work spans scheduled and unscheduled maintenance, field service, calibration, certification, and emergency response for critical equipment failures. Issuing bodies include state departments (Oregon Department of Administrative Services, California purchasing), city procurement offices (City of Orlando), and regional cooperative purchasing vehicles (Sourcewell on behalf of multiple Washington and other jurisdictions). Vendors must typically hold current autoclave certifications such as CRCST or CBSPD with demonstrated hands-on experience, and must meet ISO 9001, ISO 13485, and FDA regulatory requirements where applicable.

Recent opportunities include the State of Oregon Department of Administrative Services soliciting annual autoclave inspection, calibration, and repair services with proposals due August 17, 2026 and a maximum not-to-exceed compensation of $5 million, with 5% Oregon-fabrication preference and requirement that technicians hold current CRCST, CBSPD, or equivalent certification (RFP, due August 17, 2026). The City of Orlando issued two sole-source service plans for laboratory sterilizers under Getinge USA Sales LLC (S26-0554, due August 12, 2026, and S24-0246, due March 11, 2024), covering OEM parts, accessories, and authorized field service with ISO 13485 and FDA 510K compliance required. The State of California solicited STERILGARD Biosafety Cabinets meeting detailed technical specifications and CBE certification requirements (RFB, due May 11, 2026). Activity concentrates in Oregon, Florida, California, and Washington, with cooperative purchasing expanding reach across multiple jurisdictions and entity types.