Secondhand Mindray BeneHeart D3 Monitor Defibrillator

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: 28.07.2025

Mindray BeneHeart D3 Defibrillator Analysis Report

Device Identification and Brand/Model

The device shown in the images is a defibrillator/monitor. The “mindray” brand and “BeneHeart D3” model are clearly visible on the front panel of the product. The design, logo quality, and overall workmanship of the device suggest that the product is original.

Area of Use

This device is a professional medical device used to deliver an electrical shock to the heart in emergency medical situations, such as cardiac arrest, to restore its normal rhythm. It also functions as a monitor, capable of tracking the patient’s vital signs (such as ECG). It has an integrated design that includes manual defibrillation, AED, external pacer, and monitor modes. It is generally used in healthcare settings such as hospitals, clinics, and ambulances.

Quantity and Accessory Information

The following parts have been identified in the images:

• 1 Mindray BeneHeart D3 main unit
• 1 set of external defibrillation paddles integrated into the top of the device
• At least 1 sensor cable (clamp-style with a yellow tip) connected to the device
• Power and connection cables visible at the back of the device

General Status and Condition

The general status of the device is assessed as used. However, no significant wear or damage is observed on its casing. The fact that the indicator lights on the front panel (power and battery status) are lit green indicates that the device is receiving power and is in a basic operational state. The illumination of the green check mark light typically indicates that the device has successfully completed its self-test and is ready for use.

Physical and Mechanical Evaluation

The device’s white and gray plastic casing has a generally clean appearance. No significant cracks, fractures, or dents have been identified on the product’s casing or screen. There is only a small stain or scratch above the “BeneHeart D3” inscription. The keypad, mode selection dial, and other control buttons are physically intact and in place. The defibrillation paddles located on top of the device are seated properly in their holders. No blockages or damage are visible on the ventilation grilles.

Electronic Components and Screen Analysis

The clearest information regarding the device’s electronic components comes from the active indicator lights on the front panel. These lights indicate that the device’s electrical system and battery are active. Since the device’s screen is off, no comment can be made about its operational status, pixel defects, or any malfunctions. The buttons on the control panel are as follows:

• Mode Selection Dial: Monitor, Pacer, AED, Manual Defib
• Energy Selection: + and – buttons
• Operational Buttons: Charge, Shock, Record, Alarm Suspend, Event, Menu

Battery Status

The green illumination of the battery indicator light on the front panel signifies that there is a battery in the device and that this battery is either full or charging. It is not possible to comment on the battery’s physical condition (swelling, leakage, etc.) or its actual capacity based on the visuals.

Potential Malfunction Risk

Based on the visual inspection, no concerning issues have been detected in the device’s external condition. There are no visible crushes or peeling on the cables, nor any serious damage to the casing. The green lights on the front panel suggest that the device’s basic functions may be operational. Therefore, based on the current visual evidence, no obvious potential malfunction risk is observed. However, this assessment is solely a projection based on external appearance and does not guarantee that the device is fully functional or that it will not malfunction in the future.