Secondhand Apnea Monitor Nellcor Puritan Bennett EdenTrace II

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, please contact Medbidding engineers.

Report date: 22.06.2025

Product Analysis Report for EdenTrace II Multichannel Recording System

Basic Product Identification

• Device Identification: The images show a multichannel recording system and its integrated accessories.
• Brand and Model: The product’s brand is clearly stated as EdenTrace and the model as II.
• Originality: The labels and workmanship quality on the product indicate that it is original.
• Areas of Use: The device is used as a multichannel recording system for respiratory monitoring and similar medical measurements. The “CPAP” and “SPO2” connection points on the rear panel indicate specific uses such as sleep apnea and oxygen saturation monitoring.
• Quantity Information: There is one multichannel recording system in the images.

Condition and Evaluation

The general condition of the device is evaluated as used. Slight superficial scratches and signs of use are observed on its casing and screen. The fact that the screen on the front panel is lit green and the buttons are clearly visible gives an impression that the device might be in working condition. There are no visible large cracks or fractures in the mechanical parts or plastic components.

• Physical Deformation: There are slight scratches and discoloration on the surface of the device. No large-scale deformation or breakage has been detected.
• Mechanical Components: All buttons and connection points are in place and appear physically sound. No issues have been observed with the ventilation holes or hinges.
• Accessories: The rear panel of the device has various socket inputs. Among these, “CPAP”, “AUX”, “SPO2”, and the power input are noteworthy. No external cables or additional accessories are present in the images.
• Battery Status: No indicator or label providing information about an internal or external battery is visible in the images. Therefore, no comment can be made about the battery status based on the visuals.

Technical Information and Label Analysis

The label on the rear panel of the product contains some technical information:

• Serial Number: A full serial number cannot be read from the label.
• REF Code: The code “REF: P02220” is clearly stated on the label.
• Other Technical Information: The label also states that it is a “Multichannel Recording System”. Information that the device operates with 1.4-18V direct current (DC) for power input is also present. The manufacturer is “ResMed Corp., Eden Prairie, MN U.S.A.”. The CE mark is also present on the label.

The front panel of the device has a green-colored screen. The content or menu information of the screen cannot be clearly read from the images.

User and Warranty Information

• Size and Compatibility: Although the physical dimensions of the product can be understood from the images, there is no information about infant/child/adult compatibility on the label or the device itself.
• Year of Manufacture: There is no information regarding the year of manufacture on the label or the device.
• Documents: No invoice or warranty document is present with the product in the images.
• Usage Time: No indicator or label information about the device’s operating hours or how long it has been used is available in the images.

Malfunction and Risk Assessment

There is no clear evidence of a malfunction (broken part, error message, etc.) in the device in the images. Its general physical condition appears good, apart from minor superficial scratches. In terms of potential malfunction risk, no severe wear, corrosion, or crimped cables have been observed in the images. The external condition of the product suggests careful use. However, this assessment is based solely on visual inspection and does not provide definitive information about the device’s internal operation or performance. It is important to note that potential risks are only predictions based on visual inspection and do not mean that a malfunction will definitely occur.