Advancing Patient Safety Surrounding Medical Devices: A Health System Roadmap to Implement Unique Device Identification at the Point of Care

BACKGROUND: The US Food and Drug Administration’s Unique Device Identification System Rule of 2013 mandated manufacturers to assign unique device identifiers (UDIs) to their medical devices. Most high-risk (Class III), moderate-risk (Class II) and implantable devices now have UDIs. To achieve the ne...

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Detalles Bibliográficos
Autores principales: Wilson, Natalia A, Tcheng, James E, Graham, Jove, Drozda Jr, Joseph P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645947/
https://www.ncbi.nlm.nih.gov/pubmed/34880686
http://dx.doi.org/10.2147/MDER.S339232

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645947/
https://www.ncbi.nlm.nih.gov/pubmed/34880686
http://dx.doi.org/10.2147/MDER.S339232

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