تسجيل الدخول
تسجيل جديد
الخميس - رمضان 13, 1446
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-03-02-25-774
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
SIGNA™ Creator - SIGNA™ Explorer - SIGNA™ MR380 - SIGNA™ MR355 - SIGNA™ MR360 - Brivo MR355 - Optima MR360 MR systems
الأجهزة المتأثرة
Product Name (Affected Software Versions): SIGNA™ Creator (MR30.1, SV29.1, SV25.4, SV25.3) SIGNA™ Explorer (MR30.1, SV29.1, SV25.4, SV25.3) SIGNA™ MR380 (MR30.1, SV25.3) SIGNA™ MR355 (SV25.6, SV25.4, SV25.3) SIGNA™ MR360 (SV25.6, SV25.4, SV25.3) Brivo MR355 (SV20.2, SV23.2) Optima MR360 (SV20.2, SV23.2) Please refer to the attachment for more details.
الممثل المعتمد
General Electric Healthcare Arabia
سبب المشكلة
A scan can be resumed in the above MR systems following a Power Monitor trip when the ‘6-minute average SAR’ is above the limit indicated on the ‘SAR Display’.
الإجراء التصحيحي
You can continue using your affected MR system by following the instructions in "Actions to be taken by Customer/User" of the attachment. A GE HealthCare representative will contact you to arrange for the correction. Manufacturer action: Instructions and correction.
المرفقات
عودة للقائمة
