تسجيل الدخول
تسجيل جديد
الجمعة - جمادى الآخرة 26, 1446
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-07-11-24-667
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
Atellica IM Analyzer, ADVIA Centaur XP System, ADVIA Centaur XPT System, ADVIA Centaur CP System
الأجهزة المتأثرة
Assay (Siemens Material Number/Unique Device Identification, Kit Lot Number): Atellica IM Erythropoietin (EPO) Assay (100 Test) (10733006 / 00630414245775, Kit lot numbers ending in 046 and above) ADVIA Centaur Erythropoietin (EPO) Assay (100 Test) (10995096 / 00630414010380, Kit lot numbers ending in 045 and above) Test Code: EPO
الممثل المعتمد
Abdulrehman Algosaibi GTC
سبب المشكلة
Siemens Healthineers has restored alignment to the WHO Standard and verified the reference interval as claimed in the Instructions for Use (IFU) starting with the products listed above.
الإجراء التصحيحي
Please review this letter with your Medical Director to determine the appropriate course of action, including for any previously generated results, if applicable. Users may evaluate and implement the restored Atellica IM and ADVIA Centaur EPO Assay kit lots. Please refer to the attachment for more details. Manufacturer Action: Instructions.
المرفقات
عودة للقائمة
