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

Authors

202

  1. TL
    Thomas Lenarz

    Medizinische Hochschule Hannover, Germany

    2 publications · 101 citations

    2

    h-index

  2. RB
    Rolf‐Dieter Battmer

    Medizinische Hochschule Hannover, Germany

    2 publications · 101 citations

    2

    h-index

  3. JG
    James Giglio

    Columbia University, United States

    2 publications · 62 citations

    2

    h-index

  4. MH
    Mark H. Schoenfeld

    Yale University, United States

    2 publications · 53 citations

    2

    h-index

  5. VP
    Victor Parsonnet

    Newark Beth Israel Medical Center, United States

    2 publications · 64 citations

    2

    h-index

1–5 of 202

Venues

  1. Pacing and Clinical Electrophysiology

    PACE · 5 publications · 107 citations

    5

    h-index

  2. Otology & Neurotology

    2 publications · 83 citations

    2

    h-index

  3. JAMA

    2 publications · 65 citations

    2

    h-index

  4. Academic Emergency Medicine

    AEM · 2 publications · 62 citations

    2

    h-index

  5. PubMed

    Repository · 2 publications · 42 citations

    2

    h-index

1–5