Analysis of adverse events with Essure hysteroscopic sterilization reported to the Manufacturer and User Facility Device Experience database.

@article{AlSafi2013AnalysisOA,
  title={Analysis of adverse events with Essure hysteroscopic sterilization reported to the Manufacturer and User Facility Device Experience database.},
  author={Zain A. Al-Safi and Valerie I. Shavell and Deslyn T. G. Hobson and Jay M. Berman and Michael Peter Diamond},
  journal={Journal of minimally invasive gynecology},
  year={2013},
  volume={20 6},
  pages={825-9}
}
STUDY OBJECTIVE The Manufacturer and User Facility Device Experience database may be useful for clinicians using a Food and Drug Administration-approved medical device to identify the occurrence of adverse events and complications. We sought to analyze and investigate reports associated with the Essure hysteroscopic sterilization system (Conceptus Inc., Mountain View, CA) using this database. DESIGN Retrospective review of the Manufacturer and User Facility Device Experience database for… CONTINUE READING
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