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FDA releases guidance on reprocessing reusable medical devices

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On March 12, the U.S. Food and Drug Administration (FDA) released guidance that includes recommendations medical device manufacturers should follow for the safe and effective use of reprocessed devices. The guidance lists six criteria that should be addressed in the instructions for use with every reusable device to ensure users understand and correctly follow the reprocessing instructions. Read more.

The views and opinions expressed here are those of the author and do not necessarily reflect the opinions or recommendations of the American Nurses Association, the Editorial Advisory Board members, or the Publisher, Editors and staff of American Nurse Journal. This has not been peer reviewed.

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