The main purpose of this legislation, known as the Medical Device Electronic Labeling Act, is to update the Federal Food, Drug, and Cosmetic Act to allow more medical devices to provide their required labeling information electronically rather than in paper form. This change aims to make it easier for manufacturers to share important information about their products while ensuring that users can still access the necessary details. Key provisions of the act include the ability for manufacturers to provide required labeling solely through electronic means, such as websites or apps.