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: 30.07.2026
Report code: 1785398901
PRIMEDIC DefiMonitor Defibrillator Analysis Report
Device Identification and Brand Information
The images show a defibrillator/monitor device and its integrated accessories. The PRIMEDIC brand and DefiMonitor model are clearly visible on the front of the device. This information confirms that the device is a PRIMEDIC DefiMonitor.
Authenticity Assessment
Upon examining the logo, typography, and overall build quality on the device, the product appears to be authentic. The placement of labels and buttons reflects standard manufacturing quality.
Usage Areas
This device is a defibrillator used in the treatment of cardiac arrhythmias. It is designed to deliver an electric shock to restore the heart’s normal rhythm in emergency situations. The “ECG” and “SpO2 ALARM” indicators suggest that it possesses electrocardiography and blood oxygen saturation monitoring features. The device is suitable for use in fields such as emergency medicine, cardiology, and intensive care. Additionally, the “AED-Mode” label indicates that it can also be used in automated external defibrillator mode.
Quantity Information
- Defibrillator/Monitor Device: 1 unit
- Integrated Defibrillation Paddles: 2 units (one pair)
- Paddle Connection Cable: 1 unit (integrated, coiled)
- Power Cable: 1 unit (partially visible)
General Condition and Physical Deformation
The device is in a generally used condition. There is noticeable wear and dirt on its orange casing and black rubber edges. Specifically, white spots and scuff marks have been observed on the upper orange edge and the black rubber parts. The screen surface contains fingerprints, smudges, and light scratches. The overall condition of the device shows signs of wear due to intensive use.
Mechanical and Electronic Components
No visible fractures or cracks were detected in the mechanical components of the device, particularly on the buttons and the connection points of the paddles. However, there is dirt and wear on the surface of the buttons and the casing. Regarding the electronic components, the screen is off and does not display any images or error messages. The physical surface of the screen has smudges and scratches.
Accessories and Connection Points
The device comes with integrated defibrillation paddles and a coiled connection cable. The paddles are placed on the top of the device. A power cable is partially visible on the left side. The buttons for functions such as “ECG” and “SpO2 ALARM” on the front of the device suggest the presence of socket inputs for these functions, although the socket inputs are not clearly visible in the images. There is a gap at the bottom of the device that could be a card slot or a connection point.
Battery Status
There is no indicator or label in the images that provides direct information about the battery status of the device. The physical condition of the battery (swelling, leakage, etc.) cannot be determined from the images.
Label Information
- PRIMEDIC™: The manufacturer brand of the device.
- DefiMonitor: The model name of the device.
- ECG: Indicates the electrocardiography feature. Used to measure the electrical activity of the heart.
- SpO₂ ALARM: Indicates the blood oxygen saturation measurement and alarm feature.
- MAN: Refers to the manual defibrillation mode.
- SYNC: Refers to the synchronized defibrillation mode.
- CHARGE: The charge button; initiates energy loading for defibrillation.
- 50, 70, 100, 150, 200, 250, 300, 360 Joules: Indicates the energy levels that can be selected for defibrillation.
- AED-Mode Guidelines 2010: Indicates that the Automated External Defibrillator mode complies with 2010 guidelines.
- Power Button Symbol: Indicates the on/off button of the device.
- Battery Symbol: Points to an indicator showing the battery status.
- Plug Symbol: Indicates the external power connection.
Screen Analysis
The device’s screen is off. No text, warnings, menus, or values are visible on the screen. There is dirt, fingerprints, and light scratches on the screen surface.
Dimensions and Compatibility
There is no concrete information regarding the dimensions or user compatibility of the device in the images. However, it is understood from visual cues that the device is a portable defibrillator and is of standard size designed for emergency interventions.
Year of Manufacture
There is no direct year of manufacture label on the device. However, the “AED-Mode Guidelines 2010” label suggests that the device’s software or design dates back to at least 2010 or later. The exact year of manufacture could not be determined from the images.
Documents
No invoices, warranty certificates, user manuals, or other documents belonging to the device are visible in the images.
Usage Duration
There is no information regarding the operating hours or total usage duration on the device’s screen, labels, or any documents visible in the images.
Existing Faults
No clear evidence of a fault, such as a broken part, error message, or severed cable that would prevent the device from operating, was detected in the images. The fact that the screen is off does not indicate the current operating status of the device.
Potential Risk of Failure
The significant wear, scratches, and dirt accumulation observed on the casing and rubber edges of the device indicate long-term use. This may pose a potential risk that could lead to cosmetic or functional issues in the future. However, no direct risk of functional failure was detected in the images.
