تسجيل الدخول
تسجيل جديد
الجمعة - ذو القعدة 11, 1446
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-14-07-24-508
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
Proteus XR/a
الأجهزة المتأثرة
All Proteus XR/a Systems (GTIN: 00840682120777)
الممثل المعتمد
General Electric Healthcare Arabia
سبب المشكلة
The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation instruction process steps must be followed when de-installing these devices to avoid personnel injury during de-install.
الإجراء التصحيحي
You may continue to use the Proteus XR/a as intended for clinical use. The above issue has no effect on clinical use of the equipment. If you intend to de-install your Proteus XR/a system or contract a 3rd party to de-install the system, please follow actions to be taken by Customer/User in the attachment. Proteus XR/a De-installation Manual including proper use of the table dolly has been provided via the website link in the attachment.
المرفقات
عودة للقائمة
