Objective AI Report
Disclaimer: I am Medbidding AI. I am an unbiased AI robot. I have generated the following report automatically (without human intervention). The report was prepared by examining only the product images in the ad in detail. The report may contain errors. Medbidding and other parties disclaim any liability that may arise from this report or reliance on its contents. If you have any questions or notice an error in the report, please contact Medbidding engineers.
Report date: 23.09.2026
Report code: 1790167415
Medrad Spectris Solaris EP MR Injection System Analysis Report
Device Identification and Basic Information
The main device examined in the images is a medical injection system used for contrast media injection in medical imaging centers. The system consists of a head unit, a control panel screen, a mobile wheeled support stand, and two injector cylinders.
- Brand and Model: Medrad Spectris Solaris EP
- Device Type: Magnetic resonance compatible contrast injection system
Authenticity and Condition Analysis
Upon examination of the original brand logos, standard safety labels, and type plates, it is understood that the device is authentic. The general condition of the device is used and in working order.
- General Condition: Second-hand, used in a clinical environment
- Physical Deformation: There is slight yellowing and surface staining on the plastic body and the base of the stand. There are no cracks or fractures on the screen frame or the injector head.
- Mechanical Components: The wheeled stand mechanism, support arms, and injector slots are mechanically sound.
- Electronic Components: The control panel screen, control buttons, and power connection sockets are in place. The screen is in the off state.
Usage Areas and Compatibility
This device is used to automatically inject contrast media and physiological saline into the patient during magnetic resonance imaging (MR) scans. It is suitable for use in the radiology branch and MR units.
- Size and Compatibility: The device is of a size compatible with standard MR examination rooms and can be easily moved within the room thanks to its wheeled structure.
Quantity Information and Accessories
The total number of products and parts in the images has been meticulously counted.
- Quantity Information: 1 main injection head unit, 1 control panel screen, 1 wheeled support stand, 2 transparent injector cylinders, and 1 battery block at the bottom are present.
- Accessories: The device includes two transparent injector chambers, connection hoses, spiral cables, power cables, and a battery group integrated into the stand base. There is no data regarding the expiration dates of the accessories in the image.
Battery Status and Power Components
An external battery block is attached to the lower body of the stand. MR compatibility symbols and warning labels are located on the battery block. As far as can be understood from the image, no physical swelling or liquid leakage has been observed on the battery casing.
Label and Text Inventory
The texts, labels, and codes read from the images are listed in full below:
- Brand and Model Texts: medrad, Spectris Solaris EP, MR INJECTION SYSTEM, BAYER
- Warning and Instruction Texts: WARNING: Risk of air injection. Embolism may result in injury or death. Refer to the operator’s manual. Expel air from the fluid path to the syringe. Observe the change in FluidDot indicators. Air, Fluid. For syringes obtained from Bayer. MR SAFE (Green label).
- Code and Number Labels: The codes 60721016, REV F, MFG CHG 64223 are located on the model and serial number labels. There are cylinder positioning labels with letters B and A on the injector, along with an IPX1 protection class statement.
These labels and texts ensure that the operator uses the device safely, attaches the correct syringes, remains cautious against air bubble risks, and follows the technical revision information of the device.
Screen Analysis
The external screen unit belonging to the control panel is clearly visible in the images, but the screen illumination is off. Therefore, no active menu, error code, or instantaneous value can be read on the screen.
Production Year and Usage Duration
There is no production year printed directly on the labels. However, the design, color tones, and label format of the device are based on professional medical equipment standards, and no concrete date data regarding the production period is present in the image.
- Usage Duration: There is no counter data on the screen or labels indicating the operating hours or total usage duration of the device.
Documents
There are no invoices, warranty certificates, user manuals, or any printed documents in the images.
Existing Fault and Potential Risk Analysis
In the examination performed on the images, no evidence of an existing fault such as a broken part, severed cable, or clear error message was found.
- Potential Fault Risk: Apart from slight cosmetic stains due to age on the plastic body parts and the stand base, no serious wear, rust, or cable crushing was observed. The general physical condition of the device is at a good level.
