UNSPSC 41131610: Cell-freezing apparatus and reagents for in vitro diagnostic use

In this classification, cell-freezing apparatus and reagents for in vitro diagnostic use are devices used to freeze human red blood cells for in vitro diagnostic use. US FDA regulates Cell-freezing apparatus and reagents for in vitro diagnostic use under 21 CFR 864.9225 and under FDA product code KSP.

UNSPSC 41131610 Cell-freezing apparatus and reagents for in vitro diagnostic use is a Commodity code that state and local governments use to procure blood transfusion equipment, blood warmers, associated consumable bags, and specialized medical transport supplies for emergency medical services and clinical laboratory operations. The issuing bodies soliciting under this code include state emergency medical services boards and county health and emergency services departments, which use these purchases to equip emergency transport, hospital transfusion services, and fire rescue operations across their jurisdictions.

California's Emergency Medical Services Board (EMSB) posted a competitive solicitation (RFBIS27200126, ITB format, due September 9, 2026) for blood transfusion equipment including the Qinflow Warrior Blood Warmer system, associated consumable bags, and T-SPEC Meret Bag G2 Pro X medical transport bags for EMSB facilities statewide, with Certified Business Enterprise (CBE) certification required and best-value award criteria applied. Recent activity concentrates in California and Florida; the code shows limited but decision-relevant state and local procurement volume.