A Primer to the Structure, Content and Linkage of the FDA’s Manufacturer and User Facility Device Experience (MAUDE) Files

Eitemau Tebyg

• Reporter’s occupation and source of adverse device event reports contained in the FDA’s MAUDE database
  gan: Kavanagh, Kevin T, et al.
  Cyhoeddwyd: (2019)
• Large Eddy Simulation of FDA’s Idealized Medical Device
  gan: Delorme, Yann T., et al.
  Cyhoeddwyd: (2013)
• The Dangers of Dental Devices as reported in the FDA MAUDE Database
  gan: Hebballi, Nutan B, et al.
  Cyhoeddwyd: (2015)
• Real-World Medical Device Reports of SpaceOAR Hydrogel Spacer: Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience (MAUDE) Database
  gan: Lara Hathout, MD, et al.
  Cyhoeddwyd: (2025-12-01)
• FDA’s commitment to transparency
  gan: Guharoy, Roy, et al.
  Cyhoeddwyd: (2021)