تسجيل الدخول
تسجيل جديد
الخميس - شوال 5, 1446
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
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EN
SA-06-03-25-802
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
Procedure Packs containing Flex-Pusher II (51FP100)
الأجهزة المتأثرة
Delivery cable Flex-Pusher II (51FP100) in combination with Delivery system ODSIII 6F (98DS006 & 98US006) and ODSv1 6F (51US006) Flex-Pusher II (51FP100) is part of the Procedure Pack with REF: 29ASD06F, 29ASD07F, 29ASD09F, 29ASD10F, 71VSD06F, 89VSD08SF, 84VSD08F, 90VSD08LF
الممثل المعتمد
Al Amin Medical Instruments Co Ltd
سبب المشكلة
It has been identified by Occlutech that certain Procedure Packs containing Flex-Pusher II (51FP100) have a size recommendation of 6F for ODSIII and ODSv1 on the label of the Procedure Pack box and the sterile pouch of the implant that might lead to incompatibility.
الإجراء التصحيحي
1. Check your inventory and determine if you have any of the affected procedure packs. 2. In this case, please quarantine them and contact your direct Occlutech representative to return the products. Manufacturer action: Removal.
المرفقات
عودة للقائمة
