Cosmetic
جيدCosmetic Condition
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Overview
نظرة عامة:
طقم صيانة Lexmark 4Fuser 110-120V هو طقم صيانة لوحدة الدمج مستعمل ومتاح لقطع الغيار أو الإصلاح أو الاستخدام في صيانة المعدات.
المحتويات:
- طقم صيانة Lexmark 4Fuser 110-120V
الحالة:
حالة لقطع الغيار.
التفاصيل الفنية:
- الشركة المصنعة: ليكسمارك (Lexmark)
- اسم المنتج: طقم صيانة Lexmark 4Fuser 110-120V
- النوع: طقم صيانة وحدة الدمج (Fuser Maintenance Kit)
- الموديل / المرجع: Kit 110-120V
- رمز المنتج (SKU): G-Cir R5-R6-71N
إفصاح عن الحالة: يُباع هذا العنصر كمنتج مستعمل لقطع الغيار ولا يُعتبر جديدًا.
Technical Details
| Brand | Lexmark |
|---|---|
| Category | مجموعة صيانة وحدة الصهر |
| Medical Discipline | مختبر |
| Cosmetic Condition | جيد |
| OEM | لكسمارك |
| SKU | G-Cir R5-R6-71N |
| Warranty | لا ضمان |
Need This Product Certified Patient-Ready?
If you require this product to be patient-ready certified, you can request a quote. Inspection, testing, repair, electrical safety testing, and calibration services are available through A Biomedical Service, Inc.
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Safety & Biomedical Inspection Notice
Shipping & Receiving Notice
Medical equipment may require inspection, functional verification, calibration, preventive maintenance, safety testing, or other evaluations following transportation and before being placed into service.
Upon receipt, the purchaser is responsible for inspecting the equipment for any shipping damage and determining whether any inspection, testing, calibration, preventive maintenance, or certification is necessary based on the manufacturer's recommendations, the receiving facility's policies, and all applicable laws and regulations.
The equipment should not be placed into clinical service or used for patient care until the purchaser has verified that it is safe, appropriate, and compliant for its intended use.
Biomedical Inspection Notice
Medical equipment should be evaluated by qualified personnel before being placed into clinical service. Depending on the type of equipment, the evaluation may include, as applicable:
- Electrical safety testing
- Functional performance verification
- Alarm verification (if applicable)
- Battery inspection or replacement (if applicable)
- Calibration verification (if applicable)
- Preventive maintenance
- Software configuration and system settings
- Verification of compatible accessories, consumables, and disposables
- Inspection for shipping or handling damage
- Compliance with the manufacturer's recommendations
- Compliance with the receiving facility's policies, procedures, and applicable regulatory requirements
Transportation, storage, handling, and installation may affect the performance of medical equipment. Reuse Medical recommends that the receiving facility inspect, test, and evaluate the equipment in accordance with the manufacturer's recommendations and the facility's biomedical engineering procedures before placing the equipment into clinical service or patient use.
