UNSPSC 42221907: Cardiovascular blood flowmeters

In this classification, this commodity indicates a product used as a cardiovascular blood flowmeter in a medical setting. US FDA regulates Cardiovascular blood flowmeters under 21 CFR 870.21 and under FDA product code DPW. Most nations, for tariff and trade purposes, schedule these products under HS 901819.

UNSPSC 42221907 Cardiovascular blood flowmeters is a Commodity code that sees limited direct activity in state and local procurement. The recent opportunities block shows minimal solicitation activity explicitly tagged to this code; the one relevant match is a Hillsborough County, Florida sole source procurement for Technicuff blood pressure cuffs and hoses compatible with Stryker LP35 monitor/defibrillator equipment used by Hillsborough County Fire Rescue. Blood pressure measurement devices are the closest operational fit to the code's nominal scope, though the code's name suggests a narrower focus on flowmeters specifically. The issuing bodies pursuing cardiovascular measurement equipment tend to be health and emergency services agencies within counties and municipalities; Hillsborough County is the standout repeat buyer in the recent activity block. The broader opportunities block includes generalist law enforcement equipment, school district instructional resources, detention facility security systems, and fire rescue medical supplies, none of which align with cardiovascular blood flowmeters or blood pressure monitoring devices.

Hillsborough County, Florida is the primary jurisdiction showing relevant recent activity under this code. Hillsborough County Fire Rescue issued a sole source procurement (SS2600228) with a close date of April 13, 2026, for Technicuff 3-in-1 blood pressure cuffs and six-foot hoses in adult, pediatric, infant, and neonate sizes, with an estimated contract value of $44,385.00 for nine months through December 31, 2026. The procurement justifies sole source designation based on Technicuff Corp.'s exclusive compatibility with the Stryker LP35 system; alternative products lack validated compatibility or produce inconsistent measurements. Interested parties seeking to challenge the sole source designation were required to submit clear and convincing evidence of bona fide competition by the April 13, 2026 close date. Beyond this single relevant opportunity, the code shows no other recent state and local solicitations focused on cardiovascular measurement devices or blood flowmeters.