FDA seeks comments on medical device tracking system
OSHA Healthcare Connection, August 15, 2006
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The Food and Drug Administration (FDA) announced in the August 11 Federal Register that it is accepting comments on the use of Unique Device Identifier (UDI) systems for medical devices
UDIs-including bar code systems or radiofrequency technology-may reduce medical errors, facilitate device recalls, and improve medical device adverse event reporting, according to the FDA.
For example, a UDI could identify medical devices that are compatible, such as implanted devices that are safe to use with magnetic resonance imaging equipment.
Click here for more information about the request or how to submit electronic comments.
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