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United States · Bill · HR

H.R. 2118 (115th)

Medical Device Servicing Safety and Accountability Act

referredUnited States· United States Congress· EN

Introduced

25 April 2017

Last action

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)

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