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UDI Compliance

The U.S. FDA UDI rule on the establishment of a Unique Device Identification System requires that medical devices distributed in the U.S. must now carry a Unique Device Identifier (UDI), with some exceptions. This system will provide a standardized way to identify devices across all information sources and systems, including electronic health records and device registries.

These training courses enable you to gain a deeper understanding of the U.S. FDA Unique Device Identification Rule to advance your Class II and Class I product implementation.

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