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UDI SD Reco UDI stands for Unique Device Identifier (UDI) Single Device Recalled Device Identifier.
Manufacturers, packagers, and labelers of medical devices are required to file UDI SD Reco UDI.
UDI SD Reco UDI can be filled out online through the FDA's UDI Database.
The purpose of UDI SD Reco UDI is to provide a standardized way to identify and track medical devices that have been recalled.
The UDI SD Reco UDI must include the unique device identifier for the recalled device, information about the manufacturer, and details about the recall.
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