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Creating a Strategic Foundation of Quality Data

Siemens Healthineers takes UDI implementation to next level for its digital transformation

Using compliance with the U.S. Food and Drug Administration (FDA) Unique Device Identification (UDI) Rule as the spark, Siemens Healthineers ignited systemic data governance, data quality, and data collaboration programs and processes that promise a future continuum of value.*

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*For information about the rule, see the U.S. FDA Unique Device Identification System 

Disclaimer: GS1 US is the local GS1 Member Organization that supports implementation of the GS1 System in the United States. GS1 US employees are not representatives or agents of the U.S. FDA, and the content herein has not been reviewed, approved, or authorized by the U.S. FDA.

GS1 is a U.S. FDA-Accredited Issuing Agency for UDI, and GS1 Standards are authorized for use in implementing the requirements of the U.S. FDA UDI Rule.