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Overview
Description:
The Olympus EU-C60 EUS Exera Compact Endoscopic Ultrasound Center Processor is an electronic equipment unit designed for use with compatible Olympus endoscopic ultrasound systems. Its processor configuration serves as a central component within the EUS equipment setup, supporting system operation and integration with compatible endoscopic imaging components. The compact Exera design is intended for use in suitable clinical and medical equipment environments.
Specifications:
Brand: Olympus
Model: EU-C60
Product Line: EUS Exera
Product Type: Endoscopic Ultrasound Center Processor
Equipment Type: Ultrasound System Processor
System Type: Endoscopic Ultrasound (EUS)
Function: System Processing and Equipment Integration
Application: Compatible Olympus EUS Systems
Features:
EUS Exera processor configuration
Compact equipment design
Designed for compatible Olympus endoscopic ultrasound systems
Central system processing component
Suitable for clinical equipment environments
Technical Details
| Brand | Olympus |
|---|---|
| Category | Endoscopic Ultrasound Center Processor |
| Medical Discipline | General Surgery |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | Olympus |
| SKU | DA43-ITEM-M - P |
| Warranty | 30 - Warranty |
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.
