Secondhand Medrad Spectris Solaris EP Injector

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: 04.09.2025

Medrad Spectris Solaris EP Injector System Analysis Report

Product Identification and Area of Use

The images display an injector system used in medical imaging processes and the Magnetic Resonance (MR) device onto which this system is mounted. The analysis focuses on the Medrad Spectris Solaris EP model injector system, which is prominently featured as the main product. This device is designed for the controlled injection of liquids, such as contrast agents, into a patient during MR scans. The presence of two syringe slots on the device indicates its capability for dual-fluid injection. In the background, a Siemens brand MAGNETOM Tim and Dot System model MR device is visible.

Brand and Model Information

The brand and model of the injector system in the image are clearly legible on the device. The manufacturer’s logo is also present.

• Injector System Brand/Model: Medrad Spectris Solaris EP
• Related Company Logo: Bayer

Quantity Information

The following components have been identified in the images:

• 1 unit of Medrad Spectris Solaris EP injector system main unit
• 2 transparent injectors (syringes)
• Transparent medical tubing and connectors attached to the injectors

General Condition and State

The device appears to be installed and operational in a clinical environment. It generally gives an impression of being clean and well-maintained. No significant signs of wear or tear have been observed on the product’s surface. This suggests that the device is regularly maintained and used with care. The product’s condition, when evaluated from the images, is quite good.

Physical Deformation Examination

No deformation such as scratches, cracks, dents, or discoloration has been detected on the device’s white main casing. The inscriptions, logos, and control buttons on it are clearly legible, and no fading is present. The syringes and tubes also appear physically intact.

Mechanical and Electronic Components

The mechanical components of the device, including syringe plungers, control buttons, and tubing connection points, are visually sound. The up and down movement buttons that control the syringes are physically in place. A green status light illuminated on the device indicates that the system is powered. The checkmark below the label “HAVA DIŞARI ATILDI” (AIR EXPELLED) also indicates a system function.

Accessories and Connections

Two syringes attached to the injector system and their connected tubing sets are visible as accessories of the device. The syringe labeled “A” is filled with a dark liquid, while the one labeled “B” is filled with a transparent liquid. The green and purple connectors at the end of the tubing indicate that the connections are correctly made. The thick, flexible arm at the back of the device secures the injector system to the MR device.

Label Information and Warnings

On the front of the device, there is a warning label prepared in Turkish. The information and codes on this label are as follows:

• Warnings:
  • Risk of air injection.
  • Embolism can result in injury or death.
  • Refer to the operator’s manual.
  • Expel air from the fluid path of the syringe.
  • Observe changes in FluiDot Indicators.
  • For syringes obtained from Bayer.
• Other Codes:
  • The code 86724830 Rev. A is located in the bottom left corner of the label.
  • Also on the same label, IPX1 protection class information is present.

Potential Failure Risk

No signs of device failure or significant wear (such as crushed cables, rust, cracks in critical parts, etc.) that could lead to a potential failure are observed in the images. The overall physical condition and cleanliness of the device suggest that it is regularly checked and suitable for use. Therefore, based on visual evidence, no immediate risk of failure is anticipated.