Medical Device Electronic Labeling Act

Summary

The bill changes the Federal Food, Drug, and Cosmetic Act so manufacturers can make required device labeling available solely online, provided users can easily find it and request a paper copy at no cost. It covers all medical devices, including in‑vitro diagnostics, and gives the HHS Secretary authority to add rules or carve out exceptions. The goal is to modernize labeling while keeping safety protections.

AI-generated summary — may be incomplete or inaccurate. Verify against the official bill text.

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