S.2193 - Ensuring Safe Medical Devices for Patients

A bill to require the Food and Drug Administration to include devices in the postmarket risk identification and analysis system, to expedite the implementation of the unique device identification system for medical devices, and for other purposes. view all titles (2)

All Bill Titles

  • Official: A bill to require the Food and Drug Administration to include devices in the postmarket risk identification and analysis system, to expedite the implementation of the unique device identification system for medical devices, and for other purposes. as introduced.
  • Short: Ensuring Safe Medical Devices for Patients as introduced.

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