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: 03.06.2026
Report code: 1780495752
INSTRAMED CARDIOMAX Defibrillator/Monitor Analysis Report
Device Identification and Brand Information
The product examined in the images is a combination of a defibrillator and a patient monitor. The “INSTRAMED” logo is clearly visible on the top of the device and below the screen. The model name “CARDIOMAX” is located on the bottom left of the screen. Based on this information, it has been determined that the device is a medical device of the CARDIOMAX model belonging to the INSTRAMED brand. The phrase “bi phasic Technology” is present on the bottom right of the device, indicating that the device uses biphasic defibrillation technology.
Authenticity Assessment
Considering the quality of the logos, inscriptions, and labels on the device, as well as the overall workmanship and material structure, the impression is that the product is an original medical device. No signs of counterfeiting or low-quality workmanship have been observed.
Usage Areas
This device is designed to perform defibrillation to correct heart rhythm disorders in emergency situations and to monitor the patient’s vital signs (heart rate, pulse rate, ECG). It is particularly suitable for use in cardiology, emergency medicine, intensive care units, and pre-hospital environments such as ambulances. The device features both manual defibrillation and automated external defibrillation (AED) modes, and the energy level can be adjusted according to the patient’s condition.
Quantity Information
- Main Device: 1 unit
- Connection Cables: 2 units (one coiled, the other a two-pronged straight cable)
General Condition and Physical Deformation
The device is generally in a used condition and shows slight signs of wear consistent with its age. There is general discoloration or slight dirt accumulation on the light-colored surfaces of the casing. This is more noticeable on the carrying handle and some edge areas. There are no visible scratches, dents, or cracks on the device’s casing, screen, or other main sections. The screen surface appears clean and undamaged.
Mechanical and Electronic Components
The mechanical components of the device, including the large rotary knob used for energy selection and other control buttons (Sync, AED, Charge, Disarm, Shock), appear to be intact. No broken or missing buttons have been detected. The electronic components of the device are observed through the active and informative screen. The brightness and image quality of the screen are in good condition.
Accessories and Connection Points
There is a coiled cable connected to the left side of the device and a straight cable with red and white leads gathered on the device. No significant damage or breakage has been observed on these cables. No other accessories (such as defibrillation pads or multi-function electrodes) are visible in the images. Cable connection ports are available on the left side of the device.
Battery Status
The battery icon visible on the device screen indicates that the battery is fully charged or nearly full. No negative conditions such as physical swelling or leakage of the battery have been detected in the images.
Label Information and Technical Details
- Basic reference Monitoring: This label contains basic instructions for using the device in monitor mode: “Install the cable as indicated” and “Turn the select key to Monitor Mode.” This information helps the user set up the device correctly for patient monitoring purposes.
- Basic reference Defibrillation: This label provides step-by-step instructions for the defibrillation process: “Place the paddles,” “Select the energy scale (200, 300, 360),” “Press ‘Charge’,” and “Wait for the ‘Charge Done’ beep and press ‘shock’ or the paddles keys.” These instructions ensure that the correct defibrillation procedure is applied in emergency situations.
- Energy Levels: Different energy levels such as 1-10, 20, 30, 50, 80, 100, 150, 200, 250, 300, and 360 Joules are indicated on the device’s rotary knob. These values represent the intensity of the electric shock that can be applied during defibrillation and are adjusted according to the patient’s condition.
- Parameters on the Screen: There are abbreviations and values on the screen such as “BPM” (Beats Per Minute), “PPM” (Pulses Per Minute), and “mA” (milliampere). These parameters are used to monitor the patient’s physiological status.
- Mode Adult: The text “Mode Adult” on the bottom left of the screen indicates that the device is operating in adult patient mode or is set for this mode.
Screen Analysis
The device screen is on and displays various information. In the top left corner, there is a “Pad” indicator along with “BPM” and “3 leads” inscriptions. The values “PPM 70” and “mA 30” are located in the center of the screen. Below these values, “II PAUSE” and “DEMAND” options are visible. The warning “Bad Contact” appears prominently in capital letters in the center of the screen. In the bottom left corner, the time is shown as “09:34” and the date as “08/13/20”. The battery icon indicates full capacity. In the bottom right corner, under the heading “INFOCENTER,” there is a “Connect Multifunc Electrodes” warning. The word “ECG” is present vertically on the left edge of the screen.
Size and Compatibility
There is no metric information regarding the exact dimensions of the device in the images. However, the overall design and carrying handle of the device indicate that it is a portable medical device. The “Mode Adult” inscription on the screen indicates that the device is compatible with adult patients and is suitable for use with this patient group.
Year of Manufacture
The date “08/13/20” (August 13, 2020) visible on the device screen provides a concrete clue about the production period of the device. This date suggests that the device was manufactured in 2020 or at least was actively in use at that time.
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 total usage hours or duration on the device screen or on the labels on the device.
Current Fault
The “Bad Contact” warning is clearly visible on the screen. This is a current fault indicating an issue with the electrode connections or pads. Additionally, the “Connect Multifunc Electrodes” warning indicates that the multi-function electrodes required for the full functionality of the device are not connected or are missing.
Potential Fault Risk
The general condition of the device is good. No obvious conditions that could pose a potential fault risk, such as severe wear, rust, or cable crushing on the casing, have been observed. However, the “Bad Contact” warning on the screen indicates that the electrode connections or pads need to be checked and that this situation may constitute a potential operational issue.
