Device Failure Reporting
Device Failure Reporting is a formal postmarket surveillance mechanism that systematically documents and analyzes the malfunction or degradation of medical devices after commercial release to identify risks, ensure regulatory compliance, and support public health safety.
35
Publications
1.8K
Citations
202
Authors
133
Institutions
Publications per year
2017–2026
6
Parents
35
Tolerating hardware device failures in software
Asim Kadav, Matthew J. Renzelmann, Michael M. Swift · 2009 · 116 citations
Results With Syncardia Total Artificial Heart Beyond 1 Year
Gianluca Torregrossa, Michiel Morshuis, Robin Varghese et al. · ASAIO Journal · 2014 · 99 citations · Full text
Medicine, Cardiology, Surgery +12
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133
Medizinische Hochschule Hannover
Hanover, Germany
2 h-index
3 publications
149 citations
Yale New Haven Hospital
New Haven, United States
2 h-index
4 publications
77 citations
London Health Sciences Centre
London, Canada
2 h-index
2 publications
59 citations
Columbia University
New York, United States
2 h-index
5 publications
419 citations

University of British Columbia
Vancouver, Canada
2 h-index
2 publications
87 citations
University of California, San Francisco
San Francisco, United States
2 h-index
8 publications
858 citations
The Royal Victorian Eye & Ear Hospital
East Melbourne, Australia
2 h-index
7 publications
226 citations
University of North Carolina at Chapel Hill
Chapel Hill, United States
2 h-index
3 publications
109 citations
1–8 of 133
PACE · 5 publications · 107 citations
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2 publications · 83 citations
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2 publications · 65 citations
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AEM · 2 publications · 62 citations
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Repository · 2 publications · 42 citations
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