Objective AI Report
Disclaimer: I am Medbidding AI. I am an unbiased AI agent. 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: 07.11.2026
Report code: 1794040762
NIHON KOHDEN cardiolife TEC-7621K Device Analysis Report
Device Identification, Brand and Model Information
The analyzed medical device is a defibrillator used for emergency intervention and cardiac monitoring. Upon examination of the labels on the device body and the display panel, it is observed that the brand is NIHON KOHDEN, the model code is TEC-7621K, and the series bears the name cardiolife. This information is clearly visible on the front of the device.
Authenticity and General Condition
The device’s original logos, type labels, and industrial workmanship details indicate that it is authentic. The general condition of the device is used, and there are slight color fading and signs of wear on the outer casing.
Usage Areas
This device is used in hospital emergency departments, intensive care units, and ambulances to intervene in cardiac arrest cases, monitor the heart, and administer electric shocks. It is suitable for use by emergency medicine and cardiology departments.
Quantity Information
The images show 1 main defibrillator device, 2 orange external paddle electrodes attached to the device, 1 power cable, 1 multi-colored patient cable, and numerous disposable ECG electrode pads placed at the bottom of the device.
Physical Deformation and Mechanical Components
There are no fractures, deep cracks, or dents on the outer plastic casing of the device; however, there is slight yellowing on the light beige plastic surfaces due to age. The mechanical rotary switch, charge buttons, and paddle slots are in place and appear physically sound.
Electronic Components and Screen Analysis
The front of the device features an integrated monitor screen, and on the side, there is a rotary dial for adjusting energy levels along with charge buttons. The device screen is currently off, and no written data or error messages are visible on the display.
Accessories and Connection Ports
Two orange external defibrillation paddles are attached to the top slots of the device. There is a multi-pin socket input for the patient cable on the lower left side of the device. Additionally, numerous disposable ECG electrodes are lined up just below the device. There is no readable expiration date on these electrodes in the images. A black power cable is available to connect the device to the mains.
Battery Status
Since the internal battery is located inside the body and is not directly visible from the outside, there is no data in the images regarding the battery’s capacity, charge retention, or physical condition.
Label and Text Inventory
The texts read on the body and control panel of the device are as follows: NIHON KOHDEN, cardiolife, TEC-7621K, OPERATION PROCEDURE, MONITORING, A DANGER, A WARNING, 1, 2, 3, DISARM, AED, MONITOR, OFF, SETUP, SYNC, CHARGE AED, and numbers ranging from 2 to 360(J) indicating energy levels. There is a green calibration label on the top of the device, which reads etkin KALİBRASYON DENEYİ Muayene Hiz. San. Ve Tic. A.Ş., ID No: 0924IGH0368, Application Date: 20.09.2024, and Expiry: 20.09.2025. This label indicates that the device has undergone periodic calibration checks.
Dimensions, Compatibility, and Usage Duration
The images do not contain any measurement information regarding the physical dimensions of the device or user body compatibility. There is no usage duration information on the screen or labels indicating the total operating hours.
Manufacturing Year and Documents
There is no manufacturing year printed directly on the device labels; however, the design and label format of the device reflect professional medical device standards from a previous period. There are no invoices, warranty certificates, or printed user manuals in the images.
Existing Faults and Potential Risk of Failure
There is no clear evidence of failure in the images, such as broken parts on the casing, error warnings on the screen, severed cables, or missing components. No serious crushing, rusting, or deformation has been observed on the power cable or external cables; the general condition shows signs of regular use.
