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تسجيل جديد
الجمعة - رجب 27, 1447
مسجل لدى هيئة الحكومة الرقمية برقم:
20250728714
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تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-07-01-26-1204
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
Brilliance iCT, CT 6000, IQon Spectral CT, Spectral CT and Spectral CT 7500 systems
الأجهزة المتأثرة
Product Code (REF) (Product Model, Device Identifier): 728306 (Brilliance iCT, (01)00884838059474) 728307 (CT 6000, (01)00884838104600) 728332 (IQon Spectral CT, (01)00884838059542) 728333 (Spectral CT, (01)00884838101111) 728334 (Spectral CT 7500 on Rails, (01)00884838103627) 728340 (Spectral CT 7500 CN, (01)00884838111103) 728344 (Spectral CT 7500 Plus, (01)00884838117822) Please refer to the attachment for the affected serial numbers for each model.
الممثل المعتمد
Philips Healthcare Saudi Arabia Ltd
سبب المشكلة
A potential safety issue with the affected products, where subsystem assembly fasteners may not be torqued to specification.
الإجراء التصحيحي
Please follow "Actions that should be taken by the customer / user to prevent risks for patients or users" in the attachment. You will be contacted by Philips to schedule a time for a Philips Field Service Engineer (FSE) to visit your site and to inspect the fasteners on your system. If the inspection indicates that your system is affected, Philips will perform the correction to resolve the issue. Manufacturer's action: Instructions & correction.
المرفقات
عودة للقائمة
