UNSPSC 85323001: Diagnosis of hereditary hypogammaglobulinaemia

This classification denotes the group of activities that yields a diagnosis of Hereditary hypogammaglobulinaemia. Hereditary hypogammaglobulinaemia is listed in the World Health Organization's International Statistical Classification of Diseases and Related Health Problems or ICD-10 as a four digit category under code D80. 0

UNSPSC 85323001 Diagnosis of hereditary hypogammaglobulinaemia is a Commodity code that shows minimal alignment with actual state and local procurement activity. The code's nominal scope—diagnostic laboratory services for a rare immunological disorder—does not match the recent opportunities tagged under it. The three most recent solicitations involve diagnostic imaging system procurement (picture archiving and communication systems), special education contracted services across multiple disciplines, and temporary health professional staffing across ancillary clinical categories. These opportunities span infrastructure technology, education support services, and clinical workforce augmentation, none of which directly address hereditary hypogammaglobulinaemia diagnosis. The mismatch suggests either a tagging error in the source data or a code designation that has drifted substantially from active procurement use.

Issuing bodies in the recent record include a county hospital system (San Mateo Medical Center), an independent school district in Texas (Birdville ISD), and a county health system (Santa Clara). The geographic spread covers California and Texas, with the most recent activities posted between July and October 2026. Given the structural mismatch between the code name and the actual work being solicited, this code appears to see little relevant recent activity for practitioners pursuing diagnostic laboratory services or immunological testing contracts at the state and local level.