UNSPSC 41142030: Osmolality test system

In this classification, Osmolality test system connotes a device used to measure Osmolality levels. US FDA regulates Osmolality test system under 21 CFR 862.1540 and under FDA product code JMZ.

UNSPSC 41142030 Osmolality test system is a Commodity code under which state and local government procurement offices solicit laboratory testing reagents, equipment, and certified reference materials for forensic, toxicology, and disease-surveillance applications. The work includes direct ELISA testing kits for substance analysis, mosquito-borne disease detection systems, certified drug reference standards for forensic validation and evidentiary analysis, and DNA screening kits for state laboratory operations. Issuing bodies span state crime laboratories, state health and human services departments, county forensic laboratories, and state departments of financial and professional regulation, with Texas and Florida jurisdictions appearing as active recent buyers.

Recent opportunities include the Texas Department of Public Safety's IFB for immunalysis reagent kits (ELISA testing for controlled substances) due July 23, 2026; the Illinois Department of Financial and Professional Regulation's joint purchase master contract for mosquito testing equipment (RAMP System test kits) posted May 4, 2026 with a May 20, 2026 due date; Pinellas County, Florida's ITQ for certified drug reference standards (131 line items, ISO/IEC 17025 accredited, $49,034 in eligible federal funding under the Paul Coverdell Forensic Sciences Improvement Act) due April 23, 2026; and the Texas Health and Human Services Commission's IFB for QIAxcel and QIAamp DNA screening kits (seven line items, prior-year spend $25,050–$30,000) due January 29, 2026. Pinellas County designated SBE preference with priority consideration for submissions within the first five business days. The code shows active procurement momentum in the South and Midwest, concentrated in forensic laboratory and public health laboratory supply chains where reagent and equipment specifications are driven by accreditation standards and validated methodologies.