New Mexico Administrative Code
Title 16 - OCCUPATIONAL AND PROFESSIONAL LICENSING
Chapter 19 - PHARMACISTS
Part 14 - DEVICES; MEDICAL GAS REPACKAGERS AND SELLERS
Section 16.19.14.7 - DEFINITIONS
Current through Register Vol. 35, No. 18, September 24, 2024
A. "Device", as used in the New Mexico Drug and Cosmetic Act, is any health care product that does not achieve any of its principal intended purpose through chemical action within or on the body of man or other animal and which is not dependent upon being metabolized for achievement of any of its principal intended purposes.
B. "Board" means the New Mexico board of pharmacy.
C. "Distribution of medical gases" means the distribution of medical gas, to persons other than consumers or patients.
D. "Drug order" means a prescription drug order issued by a licensed prescriber for medical gas.
E. "FDA" means the United States Food and Drug Administration.
F. "Federal Act" means the Federal Food, Drug and Cosmetic Act.
G. "Medical gas" means:
H. "Medical gas repackager" means a person that manufactures or repackages a medical gas, which includes producing, cascading, distributing, filling, mixing, purifying, separating, transferring, and transfilling medical gases. This includes original manufacturers as defined by the FDA that repackage medical gas and have a valid registration as a drug establishment with the FDA. A medical gas manufacturer shall be issued the license type medical gas repackager.
I. "Medical gas seller" means a person licensed to distribute a medical gas to a person other than a consumer or patient, or to supply medical gases on drug orders to a patient or ultimate user.
J. "Repackage" means persons or entities manufacturing bulk medical gases or transferring gas or liquefied gas product from one container to another (e.g., liquid to gas, gas to gas, liquid to liquid).