Cosmetic
جيدCosmetic Condition
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Overview
نظرة عامة:
حوض تعويم الأنسجة الرقمي Surgipath مع الإضاءة – للاستخدام المخبري هو وحدة أو ملحق معدات مستعملة متاحة من خلال Reuse Medical.
المحتويات:
- حوض تعويم الأنسجة الرقمي Surgipath مع الإضاءة – للاستخدام المخبري
الحالة:
حالة مستعملة مع علامات طبيعية للاستخدام السابق.
التفاصيل الفنية:
- الشركة المصنعة: Reuse Medical
- اسم المنتج: حوض تعويم الأنسجة الرقمي Surgipath مع الإضاءة – للاستخدام المخبري
- النوع: الكابلات والأسلاك الطبية
- رقم تعريف المخزون: BBAD4 11
إفصاح عن الحالة: هذا المنتج مستعمل ولا يمثل على أنه جديد تمامًا.
Technical Details
| Brand | Unbranded |
|---|---|
| Category | كابلات وأسلاك طبية |
| Medical Discipline | مختبر |
| Cosmetic Condition | جيد |
| SKU | BBAD4 11 |
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.
