Medical Device Electronic Labeling Act
Official title: 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.
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Referred to the Subcommittee on Health.
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.
- Introduced in House Formatted Text PDF Formatted XML
- MEDICAL DEVICE MANUFACTURERS ASSOCIATION
- MEDICAL DEVICE MANUFACTURERS ASSOCIATION
- MEDICAL DEVICE MANUFACTURERS ASSOCIATION
- MEDICAL DEVICE MANUFACTURERS ASSOCIATION
- MEDICAL DEVICE MANUFACTURERS ASSOCIATION
- MEDICAL DEVICE MANUFACTURERS ASSOCIATION
Bodies those filers lobbied
- Centers For Medicare and Medicaid Services (CMS)
- Food & Drug Administration (FDA)
- Health & Human Services, Dept of (HHS)
- HOUSE OF REPRESENTATIVES
- SENATE
- Patent & Trademark Office (PTO)
- Commerce, Dept of (DOC)
- Centers For Disease Control & Prevention (CDC)
Cite this page
U.S. Congress. (2026). H.R. 3723: Medical Device Electronic Labeling Act. 118th Congress. Open America. https://openamerica.io/bill/118-HR-3723/
"H.R. 3723: Medical Device Electronic Labeling Act." 118th Congress, 2026, Open America, https://openamerica.io/bill/118-HR-3723/.
H.R. 3723, 118th Cong. (2026), https://openamerica.io/bill/118-HR-3723/.
[H.R. 3723: Medical Device Electronic Labeling Act](https://openamerica.io/bill/118-HR-3723/)