UNSPSC 85521202: Restriction of left vertebral vein with intraluminal device, percutaneous approach

This classification denotes the group of activities that yields a surgical intervention or procedure to restriction of left vertebral vein with intraluminal device, percutaneous approach. This surgical intervention or procedure is listed in the World Health Organization's International Statistical Classification of Diseases and Related Health Problems or ICD-10 as code 05VS3DZ

UNSPSC 85521202 Restriction of left vertebral vein with intraluminal device, percutaneous approach is a Commodity code whose scope and definition do not align with the state and local contract opportunities posted under it. The recent solicitations tagged with this code cover occupational medical surveillance services, independent disability medical evaluations, surgical benefit carve-out programs, pharmacy benefit management, temporary health professional staffing, and emergency medical services for detained youth—none of which involve vertebral vein restriction procedures or intraluminal medical devices. The code shows little relevant recent activity; state and local procurement systems appear to have misclassified these health service management and staffing opportunities under a procedure-specific medical device and intervention code.

The issuing bodies reflect typical state and local health and human services procurement: the Washington State Department of Transportation on behalf of the Washington State Ferries, Santa Clara County Health System, the City of Phoenix Retirement Office, the City of Long Beach, Harris County Juvenile Probation Department, and Collier County Board of County Commissioners. Geographic activity appears concentrated in California (Santa Clara, Long Beach), Arizona (Phoenix), Washington (Ferries), Florida (Collier), and Texas (Harris County). No opportunities posted between August 20 and September 25, 2026 represent the actual procurement of vertebral vein restriction devices or related interventional procedures under the nominal code scope. Vendors evaluating this code should verify procurement classifications directly with issuing bodies before pursuing opportunities, as the taxonomy mismatch suggests systematic data quality issues rather than genuine demand for the coded medical device or procedure.