Secondhand Respirox G2S A20 AUTOCPAP Device with Humidifier

Objective AI Report

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Report date: 25.02.2026

Respirox G2S A20 / G2S C20 Sleep and Respiratory Device Analysis Report

Device Identification and Brand Information

The medical device shown in the visuals is a positive airway pressure (PAP) therapy unit. Upon examining the device’s design, integrated humidifier chamber, and control buttons on the front panel, it has been identified as a CPAP or Auto-CPAP system. The user manual displayed with the device includes the phrase “ECE MEDİKAL” and the title “Respirox Auto CPAP/CPAP System”. The brand and model information found on the product packaging or the device itself are as follows:

• Brand: Respirox
• Model Group: G2S Series (The manual contains the designations G2S A20 / G2S C20)
• Product Type: Sleep and Respiratory Device (CPAP/Auto CPAP)
• Origin/Distributor Mark: Ece Medikal (On the manual)

Parts and Accessories Analysis

The product set in the visuals consists of the device’s main body, carrying bag, and documentation. The total parts and accessories analysis is listed below:

• 1 Main Device Body (Respirox G2S Series)
• 1 Integrated Water Chamber (Transparent humidifier tank, attached to the device)
• 1 Original Carrying Bag (Gray colored, padded protective bag)
• 1 User Manual (Inside nylon packaging, labeled “User Manual” in English/Turkish)

Missing Parts Status: The visuals do not show the power adapter, power cable, breathing tube (circuit), and patient mask required to operate the device. Only the main unit and carrying equipment are present.

General Condition and Cosmetic Inspection

The general condition of the device, in light of the visual data, is as follows:

• Case Condition: No cracks, breaks, dents, or severe physical deformation have been detected on the device’s black plastic outer casing. The surfaces appear clean.
• Screen Status: It has been observed that the factory-applied protective film (gelatin layer) is still present on the screen panel. The green pull tab located at the corner of the film in the second visual indicates that the film has not yet been removed. This situation suggests that the device may be unused or very lightly used (near new).
• Keypad and Buttons: The main navigation knob (metallic gray rotary knob) and the alarm/mute button on the left side of the front panel are physically in place. There are no signs of wear.
• Water Chamber: No calcification, dullness, or yellowing is visible in the transparent plastic water tank. The inside of the chamber is clean.

Label and Warning Sign Analysis

The white warning label located on the upper right block of the device is in Turkish and contains the following statements:

• “ATTENTION!!! DO NOT CARRY THE HUMIDIFIER UNIT WITH WATER INSIDE. OTHERWISE, YOUR DEVICE WILL BE OUT OF WARRANTY.”

Additionally, on the left side, there is the brand logo “Respirox” and a heart rhythm graph icon. The CE certification mark (CE 0123) is legible on the user manual.

Areas of Use and Compatibility

Respirox G2S series devices are used to regulate airway pressure in the treatment of Obstructive Sleep Apnea (OSA). The device is suitable for use in hospital and home care environments. The unit in the visual is designed for PAP therapy in adult patients.

Technical Details and Electronic Components

Since the device’s rear panel is not visible in the visual, the power input socket, filter area, or SD card slot could not be examined. However, the front panel design and menu buttons indicate that the device has the standard interface of the G2S platform. No blackening or signs of liquid contact are present on the visible electronic components (screen, front panel).

Potential Malfunction Risk Assessment

No physical defect or sign of malfunction that would prevent the device from operating has been detected in the visuals. The cleanliness of the humidifier chamber suggests a low risk of water leakage. The presence of the protective film on the device indicates that the screen is protected against scratches. However, due to the absence of power cables in the visual, no visual evidence can be provided regarding the device’s electrical function test (whether it turns on or off).