Device Adverse Event

Device Adverse Event is a type of adverse occurrence in the domain of medical device regulation and safety monitoring, specifically defined as any undesirable experience associated with the use of a medical device that negatively impacts patient safety, health, or device performance.

93

Publications

3.3K

Citations

708

Authors

386

Institutions

Publications per year

2017–2026

34

Variants

Medical Device Adverse Event

Authors

708

  1. JA
    John Amoore

    Edinburgh Royal Infirmary, United Kingdom

    4 publications · 151 citations

    4

    h-index

  2. TP
    Thomas P. Gross

    United States Food and Drug Administration, United States

    4 publications · 100 citations

    4

    h-index

  3. SR
    Suzanne Rich

    Center for Devices and Radiological Health, United States

    3 publications · 35 citations

    3

    h-index

  4. PI
    Paula Ingram

    NHS Lothian, United Kingdom

    2 publications · 34 citations

    2

    h-index

  5. BJ
    Brockton J. Hefflin

    Center for Devices and Radiological Health, United States

    2 publications · 60 citations

    2

    h-index

1–5 of 708

Venues

  1. PubMed

    Repository · 5 publications · 90 citations

    5

    h-index

  2. ASAIO Journal

    4 publications · 62 citations

    4

    h-index

  3. Pacing and Clinical Electrophysiology

    PACE · 3 publications · 97 citations

    3

    h-index

  4. Nursing

    3 publications · 58 citations

    3

    h-index

  5. JACC. Clinical electrophysiology

    2 publications · 94 citations

    2

    h-index

1–5