Secondhand HP CodeMaster 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: 24.04.2026
Report code: 1777016380

Hewlett Packard CodeMaster Defibrillator Analysis Report

Device Identification

The product in the images is a defibrillator device used in medical emergencies. The device has a yellow and black casing and is positioned on a transport cart.

Brand and Model

The Hewlett Packard logo and name are clearly legible on the top right corner of the device’s front panel. Directly below the screen, the model name CodeMaster is displayed. Based on this information, the brand of the device is Hewlett Packard and the model is CodeMaster.

Usage Areas

This device is used to deliver an electric shock to the heart to restore its normal rhythm in cases where the heart loses its normal rhythm (e.g., ventricular fibrillation). It is suitable for use in hospital emergency departments, intensive care units, operating rooms, and ambulances. It is one of the essential pieces of equipment in cardiology and emergency medicine departments.

Quantity Information

There is 1 Hewlett Packard CodeMaster defibrillator device in the images. Spiral cables connected to the device and one ECG cable are visible. The transport cart is also present in the image.

General Condition

The general condition of the device appears to be good. Although it is a used device, no major damage or deformation is noticeable on its casing. The device gives the impression of being clean and well-maintained.

Physical Deformation

There are no deep scratches, dents, or cracks on the yellow plastic casing or the black front panel of the device. There are no signs of color fading or excessive dirt. The screen surface appears clean and undamaged. The keypad and rotary knob are intact.

Mechanical Components

The energy selection knob (rotary knob) and all push buttons on the device are in place and appear sturdy. The wheels and drawers of the transport cart appear to be functional based on the visual evidence. The paper roll compartment cover on the top of the device is closed.

Electronic Components

Since the device’s screen is off, there is no visual data regarding its electronic operation. However, when viewed from the outside, the socket inputs and cable connections appear intact. The labels on the buttons on the front panel are legible.

Accessories

Two black spiral cables and one gray ECG cable connected to the device are visible. The paddles at the ends of the spiral cables are placed in their slots on the sides of the device. There is a patient connection connector at the end of the ECG cable. The power cable is plugged in at the back of the device. There is no information in the images regarding the expiration date of the accessories.

Battery Status

No information can be obtained from the images regarding whether the device has an internal battery or its status. The battery compartment is not visible from the outside.

Label Information

There is a code on the front panel of the device, below the rotary knob, reading M1722-64332 Rev.C. This code may be the part or revision number of the device. Detailed label information such as serial number, lot number, or REF code on the back or side surfaces of the device is not present in the images.

Screen Analysis

The device’s screen is off. Therefore, no text, warnings, or menus are visible on the screen.

Dimensions and Compatibility

There is no information on the label regarding the physical dimensions of the device or which patient group (infant/child/adult) it is suitable for. However, the values up to 360 Joules on the energy selection knob indicate that it is suitable for use on adult patients.

Year of Manufacture

There is no clear date information regarding the year of manufacture on the labels or the device in the images.

Documents

No documents such as the device’s invoice, warranty certificate, or user manual are visible in the images.

Usage Duration

There is no information (on the screen or label) in the images regarding how long the device has been used or its total operating hours.

Existing Faults

There is no clear evidence in the images, such as broken parts, missing buttons, or error messages, indicating that the device is faulty.

Potential Risk of Failure

The physical condition of the device is good. No serious wear, crushing, or damage has been observed on the casing, screen surface, or cables. This indicates that the device has been well-maintained and the risk of potential failure is low.