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Unique Device Identification (UDI) for Medical Devices - FDA
The U.S. Food and Drug Administration (FDA) is proposing a rule requiring unique device identification (UDI) for medical devices to meet the requirements of
The safety of reprocessed medical devices marketed for single
Apr 15, 2010 Reusable devices have to be designed in such a way that the key characteristics withstand the reprocessing procedure using a validated process
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