UNSPSC 42144001: Implanted hearing device external sound processors

In this classification, this commodity indicates a product providing external sound processors used in association with implanted hearing devices. US FDA regulates Implanted hearing device external sound processors under 21 CFR 874.33 and under FDA product code ESD. Most nations, for tariff and trade purposes, schedule these products under HS 901890.

UNSPSC 42144001 Implanted hearing device external sound processors is a Commodity code representing hearing aids and related auditory assistance devices procured by state and local health and human services programs. State and local governments buy these devices primarily through Medicaid-funded rehabilitation and disability-services programs that serve populations with traumatic injuries, chronic conditions, or developmental needs; the procurement typically bundles hearing aids with delivery, fitting, maintenance, and emergency repair services rather than device supply alone. The issuing bodies under this code are predominantly state Medicaid and health services agencies, particularly those operating comprehensive rehabilitation programs for specific disability populations. Scope of work encompasses device procurement at CMS DMEPOS fee-schedule pricing, in-home delivery with client and caregiver instruction, emergency repairs or replacements within 24 hours, loaner equipment during extended service, and documented training delivery.

The Texas Health and Human Services Commission (HHSC) issued RFP HHS0017173 on June 2, 2026, for Master Contracts in Durable Medical Equipment and Services supporting the Comprehensive Rehabilitation Services program across eleven geographic regions in Texas. The procurement spans multiple DME categories including communication aids and hearing aids, with contract term through August 31, 2031, and optional one-year extension; estimated compensation is approximately $1 million per state fiscal year with a cumulative cap of $5 million, though HHSC reserves discretion to increase funding. The RFP includes a 21.1 percent HUB (Historically Underutilized Business) set-aside requirement with mandatory good-faith subcontracting plans, and mandates comprehensive insurance (minimum $1 million to $2 million coverage), audited financial statements, HIPAA compliance, Medicare/Medicaid provider enrollment, and three references. Respondents must be current medical device manufacturer or distributor licensees with at least two years in business and demonstrated financial solvency; evaluation weights experience at 20 percent, demonstrated ability at 20 percent, and project work plan (client management, service delivery approach, turnaround capability) at 60 percent.