(a) In this section:
(1) “Complex rehabilitation technology equipment” means equipment that is classified as durable medical equipment under the Medicare program on January 1, 2013, configured specifically for an individual to meet the individual’s unique medical, physical, and functional needs and capabilities for basic and instrumental daily living activities, and medically necessary to prevent the individual’s hospitalization or institutionalization. The term includes a complex rehabilitation power wheelchair, highly configurable manual wheelchair, adaptive seating and positioning system, standing frame, and gait trainer.
(2) “Durable medical equipment” means equipment, including repair and replacement parts for the equipment, but excluding complex rehabilitation technology equipment, that:
(A) can withstand repeated use;
(B) is primarily and customarily used to serve a medical purpose;
(C) generally is not useful to a person in the absence of illness or injury; and
(D) is appropriate and safe for use in the home.
(b) If the commission determines that it is cost-effective, the executive commissioner by rule shall establish a program to facilitate the reuse of durable medical equipment provided to recipients under the Medicaid program.

(c) The program must include provisions for ensuring that:
(1) reused equipment meets applicable standards of functionality and sanitation; and
(2) a Medicaid recipient’s participation in the reuse program is voluntary.
(d) The program does not:
(1) waive any immunity from liability of the commission or an employee of the commission; or
(2) create a cause of action against the commission or an employee of the commission arising from the provision of reused durable medical equipment under the program.
(e) In accordance with Chapter 551 or 2001, as applicable, the executive commissioner shall provide notice of each proposed rule, adopted rule, and hearing that relates to establishing the program under this section.

Text of section effective until April 01, 2025