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| Adverse Events Associated With Synthetic Male Slings: An Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience Database | |||
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Int Neurourol J. 2021;25(2):172-176. Published online 2021 May 5 DOI: https://doi.org/10.5213/inj.2040294.147 |
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Adverse Events Associated With Synthetic Male Slings: An Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience Database International Neurourology Journal. 2021;25(2):172-176  Comparison of technical failures and patient-related adverse events associated with 3 widely used mechanical lithotripters for ERCP: insights from the U.S. Food and Drug Administration Manufacturer and User Facility Device Experience database Gastrointestinal Endoscopy. 2022;96(5):796-800 <p>Thoracic Endovascular Aortic Repair Adverse Events Reported In The Food And Drug Administration Manufacturer And User Facility Device Experience Database</p> Medical Devices: Evidence and Research. 2019;Volume 12:461-467 Safety Events With Large-Bore Mechanical Thrombectomy Devices: An Analysis of the US Food and Drug Administration Manufacturer and User Facility Device Experience Database From 2018 to 2021 Cardiovascular Revascularization Medicine. 2022;40:85-86 Analysis of adverse events with uterine artery embolization reported to the manufacturer and user facility device experience database Fertility and Sterility. 2017;108(3):e205 Deaths associated with implantable cardioverter defibrillator failure and deactivation reported in the United States Food and Drug Administration Manufacturer and User Facility Device Experience Database Heart Rhythm. 2004;1(4):399-405 CRT-600.07 Safety Events With Large-Bore Mechanical Thrombectomy Devices: An Analysis of the US Food and Drug Administration Manufacturer and User Facility Device Experience Database From 2018 to 2021 JACC: Cardiovascular Interventions. 2022;15(4):S52 Response to: “Adverse Events and Complications Associated With Intrathecal Drug Delivery Systems: Insights From the Manufacturer and User Facility Device Experience (MAUDE) Database” Neuromodulation: Technology at the Neural Interface. 2021;24(4):796-797 Reported Events Associated With Spine Robots: An Analysis of the Food and Drug Administration’s Manufacturer and User Facility Device Experience Database Global Spine Journal. 2022;219256822211261 Analysis of the US Food and Drug Administration Manufacturer and User Facility Device Experience database for adverse events involving Amplatzer septal occluder devices and comparison with the Society of Thoracic Surgery congenital cardiac surgery database The Journal of Thoracic and Cardiovascular Surgery. 2009;137(6):1334-1341 |
