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: 13.10.2025
Schiller FRED easyport Defibrillator Analysis Report
Overview and Product Description
The images show a portable defibrillator (automated external defibrillator – AED) of the Schiller brand, model FRED easyport, and its accessories. The product is used in medical emergencies, particularly in cases of sudden cardiac arrest, to restore the heart to its normal rhythm by delivering an electrical shock. The products in the image consist of one defibrillator main unit, one battery, and one carrying case. The inscriptions, logo, and overall build quality on the device indicate that the product is original.
Physical Condition and Deformation Analysis
When visually inspected, the device is in a very clean and well-maintained condition. Its overall condition is assessed as being near new and having been used very little. There are no noticeable physical defects such as scratches, cracks, dents, or discoloration on the device’s casing, screen, or buttons. All mechanical components, including the buttons, battery compartment, and the rubber feet located at the bottom of the device, are in place and appear robust. The device’s red carrying case is also clean and shows no signs of wear.
Electronics and Display Evaluation
The device’s electronic components are in working order. In one of the images, the device’s screen is shown to be on, displaying system information. The “!!! TESTING !!!” warning displayed on the screen indicates that the device is undergoing a self-test process, either upon startup or at regular intervals. This is part of the device’s normal operating procedure. Other information read from the screen is listed below:
- Device: SCHILLER EASYPORT
- Software Version (Sw CPU): V03.11B6
- Hardware Version (Hw CPU): V03.00B1
- Defi Hardware (Hw Defi): 8
- Language Version (Language): 19
- Date and Time: 16/09/25 17:35
These data confirm that the device’s electronic system is active and its basic configuration. The metal contact points in the battery compartment are clean and show no signs of oxidation or corrosion.
Battery and Accessory Details
A removable lithium battery is present with the product. No swelling, leakage, or any physical damage was observed on the battery’s outer surface. However, it is not possible to assess the battery’s remaining life or current performance based on the visuals.
- Battery Brand: Schiller
- Part Number (Art. Nr.): 2.230.292
- Technical Specifications: DC 12V 1.4Ah, Li/MnO₂
The device is presented with its original red carrying case, which features a defibrillator logo. Inside the case, there is a small pocket marked with a “PULL” strap; this pocket is typically used to store defibrillation electrodes (pads). However, since the contents of this pocket are not shown in the images, information regarding the presence, condition, and expiration dates of the pads cannot be provided.
Label and Technical Information
Important information is present on the product label located on the device’s rear surface. The inscriptions on the label are legible and include the following information:
- Brand: SCHILLER
- Place of Manufacture: MADE IN SWITZERLAND
- Type: 900-7055
- Approvals and Standards: CE 0123
- Water and Dust Protection Class: IPX4
There is no distinct indication of the product’s serial number or lot number on the label.
Conclusion and Potential Risk Assessment
In summary, the Schiller FRED easyport defibrillator device and its visible accessories are physically flawless and in very good condition. It is understood that the device operates electronically and enters test mode without issues. No adverse conditions such as rust, crushed cables, or severe wear, which would indicate an existing malfunction or pose a risk of malfunction in the near future, have been detected on the device. However, the absence of defibrillation pads, which are necessary for the device to be fully usable, in the images is a significant shortcoming. Furthermore, the battery’s performance is uncertain. For the device to be safely used on a patient, periodic calibration must be performed, and missing accessories must be supplied.
