To amend the Federal Food, Drug, and Cosmetic Act to expand the types of devices for which required labeling may be made available solely by electronic means.
Medical Device Electronic Labeling Act
This bill allows directions for use and warning labels for all medical devices to be provided electronically. Currently, this option extends only to (1) prescription devices that are used in health care facilities or by health care professionals, and (2) in vitro diagnostic devices that are used by health care professionals or in blood establishments.
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