تسجيل الدخول
تسجيل جديد
الجمعة - محرم 2, 1447
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-18-06-25-932
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
MRI Systems
الأجهزة المتأثرة
MRI Systems (Products produced after 2003) Model Name: MRT-1504/2G; S/N: 2GA1542002 Model Name: MRT-1550/I1; S/N: I1B23Z2007 Model Name: MRT-2020/S1; S/N: S1A2332001, S1A2342002, S1A2422003, S1A2422004, S1B24Y2005, S1B24Z2006.
الممثل المعتمد
Gulf Medical CO LTD
سبب المشكلة
Patients may experience auditory disturbances when using Canon MRI device without sufficient hearing protection and subsequently may report symptoms of hearing loss due to exposure to high levels of noise.
الإجراء التصحيحي
The device is equipped with a noise reduction mechanism, called Pianissimo that lowers the noise level; however, depending on the imaging method, the noise level may reach a level where hearing protection is essential. To ensure the safety of patients in using MRI System, please carefully follow the guidelines outlined in Chapter 8 of the safety manual, refer to the attachment for more details. Manufacturer Action: Instructions.
المرفقات
عودة للقائمة
