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Safe Medical Devices Act

This program reviews requirements of the Safe Medical Devices Act, which requires organizations to report adverse events caused by faulty or improperly labeled medical devices.

  • Outline reporting requirements when a patient is injured/dies due to medical device adverse events.
  • Distinguish between device adverse events that are reported to the FDA vs those reported to the manufacturer.
  • Define the penalties for non-compliance with the Safe Medical Devices Act.

   English

   Audio Included

   CE Credit Hours: 0.5 hours

   Length: 0.5 hours

   Approvers: American Nurses' Credentialing Center - ANCC

Safe Medical Devices Act

   English

   Audio Included

   CE Credit Hours: 0.5 hours

   Length: 0.5 hours

   Approvers: American Nurses' Credentialing Center - ANCC

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