UNSPSC 41142069: Urinary homocystine (nonquantitative) test system

In this classification, Urinary homocystine (nonquantitative) test system connotes a device used to measure Urinary homocystine (nonquantitative) levels. US FDA regulates Urinary homocystine (nonquantitative) test system under 21 CFR 862.1377 and under FDA product code LPS.

UNSPSC 41142069 Urinary homocystine (nonquantitative) test system is a Commodity code that currently maps to forensic drug analysis and laboratory reference materials procurement rather than homocystine testing specifically. State and local governments are buying immunoassay reagent kits, certified drug reference standards, and related analytical equipment for forensic toxicology and drug screening operations in crime laboratories and public health forensic facilities. The issuing bodies soliciting under this code include state criminal justice and public safety departments, state health and human services agencies, county forensic laboratories, and state laboratories responsible for substance analysis and evidence examination.

Recent procurement activity concentrates in Texas and Florida. The Texas Department of Public Safety Crime Lab Division posted IFB 40526R0008445A on July 9, 2026, requesting immunoassay reagent kits for Direct ELISA testing of cannabinoids, opiates, PCP, amphetamines, barbiturates, methamphetamine, cocaine, benzodiazepines, and other controlled substances, with bids due July 23, 2026. The Texas Health and Human Services Commission and Department of State Health Services posted IFB HHS0016902v2 in February 2026 for QIAxcel and QIAamp DNA screening kits, with a historical spend range of $25,050 to $30,000 annually. Pinellas County, Florida, in partnership with the Florida Department of Law Enforcement, issued ITQ 26-0305-ITQ in April 2026 for certified drug reference materials meeting ISO/IEC 17025:2017 accreditation standards, funded by the Paul Coverdell Forensic Sciences Improvement Act with approximately $49,034 designated for equipment and supplies. The code shows active quarterly procurement cycles driven by laboratory accreditation compliance, analytical method validation, and evidence analysis requirements. Illinois posted a sole-source equipment notice in May 2026 for mosquito testing systems unrelated to the nominal code scope, indicating possible miscoding in that instance.