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: 1780495750
NIHON KOHDEN TEC-5521K Defibrillator Analysis Report
Device Identification and Brand Information
The images show a medical device equipped with external defibrillation paddles. This device is a defibrillator used to deliver electric shocks for cardiac rhythm disorders. The NIHON KOHDEN brand and the ActiBiphasic cardiolife product series information are clearly visible on the device. Additionally, the label TEC-5521K is read as the model number of the device. The words APEX and SHOCK are present on the paddles.
Authenticity Assessment
The general appearance of the device, the quality of the logo, the clarity of the labels, and the integration of the components reflect professional manufacturing quality. These details suggest that the product is original.
Usage Areas
This defibrillator is used to restore normal heart rhythm by delivering a controlled electric shock to the heart in life-threatening cardiac rhythm disorders such as ventricular fibrillation (VF) or pulseless ventricular tachycardia (VT). It is of critical importance in medical branches such as emergency medicine, cardiology, intensive care units, and operating rooms. The paddles in the image are standard adult paddles used for external defibrillation.
Quantity Information
- Defibrillator Device: 1 unit
- External Defibrillation Paddles: 2 units (connected to the device)
General Condition and Physical Deformations
The device is generally in a used condition. There are slight friction marks and small stains on the white plastic casing, especially in areas near the bottom right edge and under the screen. Dust accumulations are observed in some recessed areas of the device. However, there is no serious physical deformation such as a significant scratch, dent, crack, or color fading.
Mechanical and Electronic Components
The energy selection dial, charge button, and other control buttons appear to be intact. The paddles are connected to the device, and there is no visible breakage or serious damage to their coiled cables. The device’s screen is active and displays information, which indicates that the electronic components are functional.
Accessories
Two external defibrillation paddles and the coiled cables connecting these paddles to the device are included. No other accessories (e.g., power cable, ECG electrodes) are visible in the images. There are socket inputs on the device where the paddles are attached, and these parts appear to be intact.
Battery Status
There is a “Charge battery” warning on the device screen. This indicates that the internal battery is low or needs to be charged. No physical deformation of the battery, such as swelling or leakage, was detected in the image.
Label Information
- Model Number (TEC-5521K): Indicates the specific model of the device. This code is used to define the technical specifications and compatibility of the device.
- Product Series (ActiBiphasic cardiolife): Expresses the product family to which the device belongs and the biphasic technology feature used.
- Danger Warning (DANGER):
- “Do not use defibrillator in the presence of flammable agents or concentrated oxygen.” This warning is important to prevent the risk of explosion or fire.
- “Defibrillator must be operated by trained and qualified medical personnel. Do not touch patient during defibrillation.” This warning emphasizes the critical personnel requirements and safety precautions for the correct and safe use of the device.
- Operation Procedure (OPERATION PROCEDURE): Contains brief instructions regarding energy selection and discharge steps.
Screen Analysis
The device’s screen is active and displays information in green on a black background. In the top left corner of the screen, the text “VF/VTX” (Ventricular Fibrillation/Ventricular Tachycardia) and the “x1” indicator below it are visible. In the upper middle part of the screen, “0 PADDLE” (0 Joule paddle) and “Charge battery” warnings are located. A clock display showing “13:32” is visible in the bottom right corner of the screen. At the bottom, there are menu options such as “Lead”, “Sens”, and “Alarm Setup”. In the middle of the screen, a flat green line represents the absence of an ECG signal or a flatline condition.
Dimensions and Compatibility
There is no information regarding the specific dimensions of the device in the images. However, as a portable defibrillator, it is designed for rapid intervention in emergency situations. The paddles are of standard size suitable for use on adult patients.
Year of Manufacture
There is no concrete label or document regarding the year of manufacture of the device in the images. While the general design and screen technology of the device suggest a modern appearance, a definitive determination of the year of manufacture cannot be made based on visual evidence.
Documents
No documents such as invoices, warranty certificates, or user manuals belonging to the device are visible in the images.
Usage Duration
No information regarding the usage hours or total operating time was detected on the device’s screen, labels, or any document present in the images.
Existing Faults
There is no evidence of a significant fault such as a broken part, severed cable, or missing component in the images. The “Charge battery” warning on the screen is a condition indicating that the battery needs to be charged, not a direct fault.
Potential Risk of Failure
Apart from slight friction marks on the casing, no concrete situation that could pose a potential risk of failure, such as serious wear, rust, or cable crushing, has been observed. Its general condition is good.
