Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Medrad Spectris Solaris EP MR Injection System Cat # 3012011 is a specialized equipment system designed for use with compatible magnetic resonance imaging (MRI) setups. Its electronic injection system configuration provides controlled operation and integration with compatible MR imaging equipment. The Spectris Solaris EP platform features a dedicated control interface and equipment design intended for use in suitable medical imaging environments.
Specifications:
Brand: Medrad
Product Line: Spectris Solaris EP
Product Type: MR Injection System
Catalog Number: 3012011
Equipment Type: MRI Injection System
System Type: Magnetic Resonance Compatible
Function: Controlled Injection System Operation
Application: Compatible MRI Equipment Setups
Features:
Spectris Solaris EP system configuration
Designed for compatible MR imaging environments
Electronic control interface
Specialized medical imaging equipment design
Suitable for compatible MRI system integration
Technical Details
| Brand | Medrad |
|---|---|
| Category | MR Injection System |
| Medical Discipline | Radiology |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Medrad |
| SKU | DA431-ITEM-H |
| 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.
