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Statement from FDA for Devices and Radiological Health, on FDA’s updates to Medical Device Safety A
date:Nov 21, 2018
l surveillance system would not be possible without the FDAs establishment in recent years of a unique device identification (UDI) system, in which medical devices are marked on their labels with a unique code that can be used to track the device through its distribution and use in patients. These identifiers are stored in a public database, which now contains more than 1.5 million device records, that enables patients and health care providers to download information about their devices. Patien

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