CrossRef Text and Data Mining
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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
Hanson Zhao, Colby P. Souders, Paige K. Kuhlmann, Kai Dallas, Karyn Eilber, Jennifer T. Anger
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   Crossref logo
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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   Crossref logo
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<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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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