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May 31, 2024 · The Manufacturer and User Facility Device Experience (MAUDE) database is a searchable database of medical device reports (MDRs) of adverse events involving medical devices over the last ten years. Reports older than ten years are provided on the FDA's MDR Data Files webpage. The MAUDE database: Is updated every month to include reports received ...
What happens when Carol (Adrienne Barbeau) reveals to her mother (Beatrice Arthur) that she has been seeing a therapist? Find out in the pilot episode of Mau...
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May 1, 2024 · The public MAUDE provides access to 1704 Device Problem Codes and 998 Patient Problem Codes used to characterize issues in the MDR reports. These codes were searched and sorted. Within the Device Problem Codes, code 2993, “adverse event without identified device or use problem”, was the only code used to directly identify adverse events (AEs) and was used as the sole source of reported AEs for this analysis.
Jul 17, 2020 · Atherectomy, Coronary / adverse effects*. Coronary Artery Disease / diagnostic imaging. Coronary Artery Disease / therapy*. Humans. Treatment Outcome. United States. Vascular Calcification / diagnostic imaging. Vascular Calcification / therapy*. Adverse events with orbital atherectomy: an analytic review of the MAUDE database.
6 days ago · The Manufacturer and User Facility Device Experience (MAUDE) database is a searchable database of medical device reports (MDRs) of adverse events involving medical devices over the last ten years. Reports older than ten years are provided on the FDA's MDR Data Files webpage. The MAUDE database: Is updated every month to include reports received ...
The Manufacturer And User Facility Device Experience database is a reporting software and does not independently verify the details of complications. Results: Two thousand five hundred forty reports were issued, of which 287 were patient adverse events and 2766 were device problems. Activation, separation, and positioning issues were most common.
May 29, 2024 · Post-marketing surveillance data for the esophageal SEMSs were analyzed using the FDA's MAUDE database from January 2014 to December 10, 2023. The outcomes of interest were patient-related adverse events and device failures. Statistical analysis was performed using Microsoft Excel 2010 and SPSS.
