Search FDA MAUDE (Manufacturer and User Facility Device Experience) Database
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Adverse Events By Manufacturer
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Adverse Event Overview
| Problem | Event Type | Problem Flag | Adv Evt Flag | Product Code | Medical Spec | Device Class | Device Name | Model No | Catalog No | Regulation | PMA/510K No | UDI | Mfg Name | Registration | FEI No | Report No | MDR Text | Count |
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