A comprehensive analysis of MRI‐related Cochlear implant adverse events reported by FDA's manufacturer and user facility device experience database

Abstract Objective Identify MRI‐related cochlear implant (CI) adverse events from the Food and Drug Administration (FDA) Manufacturer and User Facility Device Experience (MAUDE) database and determine whether devices with diametric magnets are associated with reduced adverse events. Methods Data on...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Laryngoscope Investigative Otolaryngology
المؤلفون الرئيسيون: Amy Lin, Arjun K. Menta, Syed Ameen Ahmad, Aileen Zhang, Dianela Perdomo, Ashwin Reddy, Bryan K. Ward
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Wiley 2025-02-01
الموضوعات:
cochlear implant
diametric magnet
medical device
الوصول للمادة أونلاين:https://doi.org/10.1002/lio2.70073

الانترنت

https://doi.org/10.1002/lio2.70073

مواد مشابهة