Meeting Unique Device Identification (UDI) Requirements with Laser Marking
In 2013 the FDA enacted a final rule requiring that most medical devices distributed in the U.S. carry a unique device identifier (UDI) to improve enhanced quality of information and tracking of medical devices. The UDI will be required to be marked directly on the device itself if it is intended to be used more than once and intended to be reprocessed before each use.
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