United States · Bill · HR
H.R. 2118 (115th)
Medical Device Servicing Safety and Accountability Act
Introduced
25 April 2017
Last action
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Status
Referred to the Subcommittee on Health.
Sponsors
—
Subjects
Discovery layer
Source updated
11 August 2025
Summary
Medical Device Servicing Safety and Accountability Act This bill amends the Federal Food, Drug, and Cosmetic Act to require establishments servicing medical devices to register with the Food and Drug Administration (FDA). Such establishments must maintain records and make reports as the FDA requires to ensure the safety and effectiveness of serviced devices. The bill exempts certain medical facilities, including physician's offices, that service medical devices in accordance with state and local laws.
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Documents
3 official files
Introduced in House (text)
Introduced in House (text)
Introduced in House · EN · 25 April 2017
Introduced in House (PDF)
Introduced in House · EN · 25 April 2017
Introduced in House
summary · EN · 25 April 2017
Sponsors
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Sources
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- Official source: https://www.congress.gov/bill/115th-congress/house-bill/2118
- Open data entity: https://api.congress.gov/v3/bill/115/hr/2118