Unique device identification and traceability for medical software: A major challenge for manufacturers in an ever-evolving marketplace.

Journal of Biomedical Informatics(2019)

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摘要
•UDI has been introduced with the new European Regulations for medical devices.•The impact of UDI on software development is of particular interest.•Labeling, privacy, assignment criteria, and standards should be considered.•These aspects can be managed to effectively pursue the medical device traceability.
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关键词
UDI,EUDAMED,Software medical device,Medical Device Directive 93/42/CEE,Medical Device Regulation (UE) 2017/745,Traceability
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