The European Commission’s Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) 6th meeting of the Working Group on Reprocessing of Single-Use Medical Devices released minutes from the March 10, 2010 meeting.  At AMDR, we believe it is crucially important that Europe employ a reasonable regulatory model for “single-use” medical device reprocessing that provides hospitals access to safe, regulated, lower-cost and environmentally-responsible reprocessed devices.  We hope AMDR can be of service in providing necessary information on these subject matters, and we are certain FDA’s expertise in this area is essential to ensuring the SCENIHR has access to accurate information on the subject.