Reprocess (i - gpo 2025

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The document is a notice from the FDA regarding a public workshop focused on the reprocessing of reusable medical devices. It highlights the importance of proper cleaning and sterilization to prevent healthcare-associated infections (HAIs) and outlines the FDA's initiative to improve device design, reprocessing procedures, and validation methodologies. The workshop aims to discuss issues related to reprocessing quality, device design, and best practices in healthcare settings. Participants are encouraged to register for the workshop and submit comments.

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Reprocess (i - gpo 2025

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