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
Parents
93
Adverse Events With Transvenous Implantable Cardioverter-Defibrillators
Mårten Rosenqvist, Thorsten Beyer, Michael S. Block et al. · Circulation · 1998 · 232 citations
Medicine, Cardiology, Surgery +16
Safety Issues Involving Medical Devices
William H. Maisel · JAMA · 2005 · 104 citations
1–5 of 93
708
4
h-index
United States Food and Drug Administration, United States
4 publications · 100 citations
4
h-index
3
h-index
2
h-index
Center for Devices and Radiological Health, United States
2 publications · 60 citations
2
h-index
1–5 of 708
386
Center for Devices and Radiological Health
Rockville, United States
9 h-index
12 publications
301 citations
Harvard University
Cambridge, United States
5 h-index
16 publications
860 citations
Maastricht University
Maastricht, The Netherlands
4 h-index
12 publications
1.6K citations
The Ohio State University Wexner Medical Center
Columbus, United States
4 h-index
4 publications
181 citations

University of British Columbia
Vancouver, Canada
3 h-index
11 publications
399 citations
United States Food and Drug Administration
Silver Spring, United States
3 h-index
6 publications
182 citations
Cleveland Clinic
Cleveland, United States
3 h-index
3 publications
201 citations

Western University
London, Canada
3 h-index
4 publications
183 citations
1–8 of 386
Repository · 5 publications · 90 citations
5
h-index
4 publications · 62 citations
4
h-index
PACE · 3 publications · 97 citations
3
h-index
3 publications · 58 citations
3
h-index
2 publications · 94 citations
2
h-index
1–5