Secondhand Comen C50 Patient Monitor

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: 05.09.2025

Comen C50 Bedside Patient Monitor Analysis Report

Product Description and Content

The images show a bedside patient monitor used in medical environments and a blood pressure cuff belonging to this monitor. The products are generally observed to be used. The report is based on the visual analysis of these two items.

Package contents are listed below:

• 1 Comen C50 Bedside Patient Monitor
• 1 Yaşam Medikal Blood Pressure Cuff (cuff) and hose

Brand and Model Identification

During the detailed examination, the brand and model information of the device and its accessory have been clearly identified from the images.

• Monitor Brand and Model: Comen C50 is clearly visible in the upper right corner of the device’s front bezel.
• Blood Pressure Cuff Brand: The blue blood pressure cuff features the Yaşam Medikal brand logo and name, along with a CE mark.

Physical Condition and Cosmetic Assessment

Although the general condition of the device indicates it has been used, no obvious damage pointing to a functional problem has been observed. The device casing is beige. The most prominent physical deformation is a sticky residue or surface abrasion on the bezel to the right of the screen. This is a cosmetic flaw and does not appear to affect the device’s operation. No significant scratches, cracks, or discoloration are noticeable on other parts of the device or the blood pressure cuff.

Functionality and Screen Analysis

The monitor’s screen is active, displaying various physiological parameters and menu options. This indicates that the device’s main electronic components are functioning. The observations on the screen are as follows:

• Patient Mode: The patient mode is displayed as “YETŞK” (Adult) at the top of the screen.
• Date and Time: The date “1986-12-31” visible on the screen suggests that the device’s settings have been reset or that the internal clock battery needs replacement.
• Parameters: The screen displays ECG (Electrocardiography) and PLETH (Plethysmography) waveforms, as well as numerical value fields for NIBP (Non-invasive Blood Pressure), SPO2 (Blood Oxygen Saturation), and PR (Pulse Rate).
• Warning Message: The warning “SPO2 SENSÖR OFF” is displayed at the top of the screen. This is not an error code; it is a standard informational message indicating that the SPO2 sensor is not connected to the device.
• Control Buttons: At the bottom of the screen, there are Turkish control menus such as SESSİZLİK (MUTE), TREND GRAFİ (TREND GRAPH), KAYIT (RECORD), and SİSTEM MENÜ (SYSTEM MENU).

Accessories and Ports

The images show one Yaşam Medikal brand blood pressure cuff and its hose included with the device. The hose is connected to the NIBP input on the device’s side panel.

The device’s side panel features numerous ports for various sensor and accessory connections. These ports are:

• NIBP: Blood pressure cuff connection (in use).
• ECG1 / ECG2: ECG cable connections.
• SPO2: Oxygen saturation sensor connection.
• CO2/AG: Carbon dioxide/Anesthetic gas sensor connection.
• TEMP1 / TEMP2: Body temperature probe connections (protective caps attached).
• ICG and IBP1 / IBP2: Inputs for other parameters (protective caps attached).

Potential Risk Assessment

It is understood that the device is operational and performs its basic functions. Cosmetically, there is no serious physical damage other than the abrasion on the screen bezel. The “SPO2 SENSÖR OFF” warning displayed on the screen merely indicates that the relevant accessory is not connected and is not a sign of malfunction. An incorrect date setting on the device usually results from a weakened internal battery and is easily correctable. As far as can be understood from the images, the current state and condition of the device do not pose an immediate risk of malfunction that would prevent its use.