S 4519

This bill, the Medical Device Electronic Labeling Act, aims to allow manufacturers to provide required labeling information for medical devices electronically, rather than solely in paper form. It updates regulations within the Food, Drug, and Cosmetic Act to accommodate electronic labeling while ensuring users still have access to paper copies upon request and that essential safety information is clearly displayed. The bill also establishes a process for the Secretary of Health and Human Services to create additional requirements or exceptions for device labeling to ensure patient safety.