Defective Secondhand Life-Point Pro AED 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: 29.07.2025

Life Point Pro AED Automated External Defibrillator Analysis Report

Brand and Model Identification

The device shown in the images has been identified as a Life Point brand Pro AED model Automated External Defibrillator (AED). The Life Point logo and name are clearly visible on the device and its carrying case. The model name was determined based on the device’s general design and interface, and confirmed through research. The device is considered to be original.

Device Purpose and Areas of Use

This device is a life-saving medical device designed to analyze a patient’s heart rhythm and deliver an electric shock (defibrillation) when necessary in cases of sudden cardiac arrest. It is intended for use in emergencies by both first aid-trained individuals and untrained users, thanks to its three-step audio and visual guidance. The device is suitable for use on adult and pediatric patients, but requires the attachment of appropriate pads for use.

Set Contents and Quantity Information

The set shown in the images consists of the following parts:

• 1 Unit – Life Point Pro AED main unit
• 1 Unit – Yellow, original carrying case with logo
• 1 Unit – Red-colored fastening strap
• 1 Unit – Defibrillator pad in a package
• 1 Unit – Disposable glove in a bag

General Status and Condition Assessment

The device appears to be generally used. While the main defibrillator unit has a clean and well-maintained appearance, the outer yellow carrying case shows wear and tear from use. There is a label on the device dated “12-2023”; this label may indicate a maintenance, calibration, or last inspection date. The overall condition of the device is good, apart from cosmetic defects.

Physical and Mechanical Condition

Upon examination of the product’s physical and mechanical condition, the following details were observed:

• Carrying Case: The outer surface and corners of the yellow plastic case have multiple scratches and scuff marks. The black plastic part on the front also shows signs of wear. The “AED” lettering on the case is partially faded in places.
• Main Unit: No cracks, breaks, or significant deformations were observed on the casing of the defibrillator device. Its surface is generally clean.
• Mechanical Parts: The lock and hinge mechanism of the carrying case and the buckle of the red fastening strap appear visually intact and functional. The “ON/OFF” and “SHOCK” buttons on the device are physically in sound condition.

Accessories and Electronic Components

The device’s accessories and electronic components have been visually inspected. Inside the case lid, there is a pair of defibrillator pads in a package and a pair of gloves in a separate bag. Details such as the expiration date on the pad package cannot be discerned. The socket input on the top of the device where the pads connect appears clean and undamaged. Since the device is turned off, there is no image or warning on its screen. The schematic diagram and icons on the front panel, showing steps 1-2-3, are clear.

Label and Technical Information

Labels containing detailed technical information such as the device’s serial number, lot number, or REF code could not be legibly viewed in the images. The only legible label on the device is a round one with the date “12-2023”. The label inside the carrying case lid contains pictograms showing the steps for use.

Potential Risk Assessment

There is no visible serious damage or wear on the main unit of the device, which indicates that its physical condition is good. The scratches and wear on the outer carrying case are purely cosmetic and do not pose a risk to the device’s functionality. However, as with any second-hand medical device, the lifespan and condition of the defibrillator pads and the internal battery are uncertain. The pads are single-use and have expiration dates; batteries also have a specific lifespan. While the meaning of the “12-2023” label on the device is not certain, it might indicate the next maintenance or consumable replacement date. These assessments are a forecast based solely on visual inspection and do not constitute a definitive fault diagnosis. It is recommended that the device be checked by a professional technical service, calibrated, and the condition of its consumables (pads and battery) confirmed to ensure it can be used safely in an emergency.