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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  <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 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 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 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 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 DEVICE RELATED PROBLEMS AND PATIENT RELATED ADVERSE EVENTS WITH SPYGLASS CHOLANGIOSCOPE: A MANUFACTURER AND USER FACILITY DEVICE EXPERIENCE (MAUDE) DATABASE ANALYSIS Gastrointestinal Endoscopy. 2022;95(6):AB302-AB303 Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience Database for Patient- and Circuit-Related Adverse Events Involving Extracorporeal Membrane Oxygenation Cardiovascular Revascularization Medicine. 2020;21(2):230-234 |
