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AMDR is the global trade association representing the legal, regulatory and other interests of regulated, commercial “single-use” medical device (SUD) reprocessing industry. AMDR members provide reprocessed and re-manufactured single-use devices to a majority of U.S. hospitals and German Academic medical centers. AMDR members support only safe, regulated SUD reprocessing and re-manufacturing. The U.S. has long regulated the reuse of SUDs as a manufacturing activity, subject to the agency’s full set of medical device manufacturer requirements. AMDR welcomes similar treatment in the forthcoming EU Medical Device Regulation. For more information on AMDR, please visit www.amdr.org