Secondhand Artema Cardio-Aid 100 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: 02.08.2025

Artema Cardio-Aid 100 Defibrillator Device Analysis Report

Overview and Device Identification

The product shown in the images consists of a defibrillator device and a pair of defibrillator paddles attached to it. The device is a medical instrument that offers both manual and semi-automatic defibrillation functions, as well as ECG (electrocardiography) monitoring capabilities. It is understood that the product is used to deliver an electric shock to patients experiencing cardiac arrest or abnormal heart rhythms in emergency situations, with the aim of restoring a normal rhythm. The instructional icons and text on the device describe its use in situations such as loss of consciousness, respiratory arrest, and the absence of a pulse.

Brand and Model

Upon examination of the images, it is clearly seen that the brand of the device is Artema and the model is Cardio-Aid 100. This information is written in large letters on the front panel of the device. The product’s logo and typography give the impression that it is an original device.

Physical Condition and Deformation Analysis

The device is generally in a used condition. Upon detailed examination of its physical state, the following points have been identified:

• Casing: The yellow plastic casing of the device shows minor dirt and stains due to use. Particularly on the control panel, a noticeable wear and surface deformation is visible in the section next to the “OFF” and alarm silence buttons. There are also minor scratches and scuff marks on the corners and edges of the device. However, no cracks or breaks were detected in the casing.
• Screen: The device’s screen is off. No cracks, deep scratches, or stains are observed on the screen surface. It appears to be physically intact.
• Keypad: All buttons on the control panel are physically in place. There is slight color fading and wear around some buttons, but no damage that would impede their function is apparent.

Mechanical and Electronic Components Inspection

No specific issues were identified during the visual inspection of the device’s mechanical and electronic components. The defibrillator paddles fit properly into their integrated holders on the device. The orange “shock” buttons located on the paddles are physically intact. The coiled cables connecting the paddles to the device show no signs of disconnection, crushing, or deformation. The external power and charging input, labeled “Ext. Power / Chg.”, and the paddle connection sockets appear clean and undamaged. As the device is turned off, no comment can be made regarding the functionality of its electronic components.

Accessories and Battery Status

The images show the device’s main accessory, a pair of defibrillator paddles, which are present and connected to the device. No other accessories, such as electrode cables for ECG monitoring or an external power/charging cable, are visible. The device features “ON/BATT1” and “ON/BATT2” buttons, designed for two separate batteries. This indicates that the device can operate with dual batteries. However, it is not possible to determine from the images whether the batteries are present or to ascertain their condition (e.g., swelling, leakage).

Label Information and Calibration Status

There is one calibration sticker on the device. The information obtained from this sticker is listed below:

• Sticker Type: TRK-TÜRKKAL KALİBRASYON
• Report No: 150700839
• Application Date: 07.2015
• Expiry Date: 07.2016

This sticker indicates that the last known calibration of the device was performed in July 2015 and its validity expired in July 2016. No other labels or markings containing technical information such as the device’s serial number, REF code, or year of manufacture could be identified in the images.

Potential Risk Assessment

The physical condition of the device is generally good, with no serious damage or wear observed. However, the most significant potential risk is that the device’s calibration period is considerably expired, as indicated on the calibration sticker. Regular calibration is a critical requirement for a life-saving device like a defibrillator to ensure it can deliver shocks at the correct energy levels and in a timely manner. In its current state, there is no guarantee that the device will operate at its specified performance, and it must be inspected and calibrated by an authorized service before use.