Ce Marking

CE Marking is a regulatory conformity indicator affixed to in vitro diagnostic medical devices signifying compliance with the essential requirements of the European Union’s In Vitro Diagnostic Regulation, thereby permitting marketing and distribution within the European Economic Area.

64

Publications

2.1K

Citations

661

Authors

201

Institutions

Publications per year

2017–2026

28

Variants

Ce Mark

Authors

661

  1. CW
    Claudia Wild

    Austrian Institute for Health Technology Assessment GmbH, Austria

    3 publications · 86 citations

    3

    h-index

  2. LS
    L. Simonetti

    Ospedale Bellaria, Italy

    2 publications · 75 citations

    2

    h-index

  3. CI
    Chong Il Yoo

    Pusan National University Hospital, South Korea

    2 publications · 112 citations

    2

    h-index

  4. HT
    Hui Taek Kim

    Pusan National University Hospital, South Korea

    2 publications · 112 citations

    2

    h-index

  5. JD
    Jan D. Schmitto

    Medizinische Hochschule Hannover, Germany

    2 publications · 87 citations

    2

    h-index

1–5 of 661

Venues

  1. EuroIntervention

    4 publications · 158 citations

    4

    h-index

  2. BMJ

    2 publications · 64 citations

    2

    h-index

  3. Expert Review of Medical Devices

    2 publications · 59 citations

    2

    h-index

  4. Multimedia Manual of Cardio-Thoracic Surgery

    MMCTS · 2 publications · 25 citations

    2

    h-index

  5. Journal of Clinical Microbiology

    JCM · 2 publications · 93 citations

    2

    h-index

1–5