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Overview
Description:
The Medrad Mark V ProVis RD Contrast Injector Control Panel Console is a specialized equipment control interface designed for use with compatible Medrad Mark V ProVis contrast injector systems. The console provides an operator interface for accessing and managing the system's available controls and operating settings. Its dedicated configuration supports integration with the corresponding contrast injector platform, making it suitable for compatible medical imaging equipment environments.
Specifications:
Brand: Medrad
Model: Mark V ProVis RD
Product Type: Contrast Injector Control Panel Console
Equipment Type: Medical Imaging Equipment Component
Component Type: Control Panel / Operator Console
Function: System Control and Operation Interface
Compatible System: Medrad Mark V ProVis
Application: Medical Imaging / Radiology Equipment
Features:
Dedicated control panel console configuration
Designed for compatible Medrad Mark V ProVis systems
Operator interface design
System control functionality
Medical imaging equipment component
Suitable for compatible radiology equipment setups
Technical Details
| Brand | Medrad |
|---|---|
| Category | Contrast Injector Control Panel Console |
| Medical Discipline | Radiology |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | Medrad |
| SKU | DA451-ITEM-N - 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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No similar items available.
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.
