Advancing Patient Safety Surrounding Medical Devices: Barriers, Strategies, and Next Steps in Health System Implementation of Unique Device Identifiers

BACKGROUND: The requirement for medical device manufacturers to label their devices with a unique device identifier (UDI) was formalized by the 2013 US Food and Drug Administration Unique Device Identification System Rule. However, parallel regulatory requirement for US health systems to use UDIs, p...

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Detalles Bibliográficos
Autores principales: Wilson, Natalia A, Tcheng, James E, Graham, Jove, Drozda, Joseph P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233486/
https://www.ncbi.nlm.nih.gov/pubmed/35761948
http://dx.doi.org/10.2147/MDER.S364539

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