Objective AI Report
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Report date: 25.06.2026
Report code: 1782371638
RESMED AirSense 10 AutoSet CPAP Device and Accessories Analysis Report
Device and Accessory Identification
The images show one RESMED AirSense 10 AutoSet CPAP device, one RESMED HumidAir Cleanable II humidifier chamber, two RESMED AirFit F20 full face masks, and one breathing tube.
Brand and Model Information
- Device: RESMED AirSense 10 AutoSet
- Humidifier Chamber: RESMED HumidAir Cleanable II
- Mask: RESMED AirFit F20
Authenticity Assessment
The RESMED logo and labels are clearly visible on the products. The CE 0123 mark is present on the humidifier chamber box. The quality of workmanship and label details suggest that the products are authentic.
Usage Areas
This set is designed for positive airway pressure (CPAP) therapy in patients with sleep apnea or respiratory failure. The device helps reduce airway dryness with its integrated humidifier feature. It can be used in home or clinical settings. It is suitable for use in respiratory therapy and sleep medicine departments. The mask and tube are essential accessories for the device.
Quantity Information
- CPAP Device: 1 unit
- Humidifier Chamber (boxed): 1 unit
- Full Face Mask (boxed): 1 unit
- Full Face Mask (unboxed, in transparent packaging): 1 unit
- Breathing Tube (in transparent packaging): 1 unit
There are a total of 1 device and 4 accessories.
General Condition and Physical Deformation
The general condition of the device and accessories appears to be good. There is a “myAir” label on the device. There are no signs of significant wear on the humidifier chamber and mask boxes. No scratches, dents, cracks, or discoloration have been observed on the device casing, screen, or other parts. There is no accumulation of dirt or dust.
Mechanical and Electronic Components
The buttons, the rotary control dial, and the connection points of the humidifier chamber appear visually intact. No mechanical deformation has been detected on the mask and tube. The internal parts of the device’s electronic components are not visible. The screen and control buttons on the outer casing are intact.
Condition of Accessories
The RESMED HumidAir Cleanable II humidifier chamber is in its original box. The RESMED AirFit F20 full face mask is in its original box. Additionally, one more RESMED AirFit F20 full face mask and one breathing tube are available in transparent packaging. There is a socket input for the humidifier chamber on the device. The expiration date is stated as 2025-10-27 on the humidifier chamber label.
Battery Status
No information regarding the internal or external battery of the device or any battery condition (swelling, leakage, etc.) has been observed in the images.
Label Information
- REF Code: 37471. This code indicates the catalog or reference number of the product. It is used for the correct identification and ordering of the product.
- LOT Number: (10)1539665. This number indicates the batch or serial number of the product. It is used for production tracking, quality control, and in cases of product recalls.
- UDI: (01)09396995005886 (11)251027 (10)1539665. Stands for Unique Device Identification. It enables global identification of the device and increases the traceability of medical devices.
- CE 0123: This mark indicates that the product complies with the European Union’s health, safety, and environmental protection standards. “0123” is the identification number of the notified body that performed the conformity assessment of the product.
- MADE IN AUSTRALIA: Indicates that the product was manufactured in Australia.
- Usage Period (Expiration Date): 2025-10-27. This date indicates the last date the product can be used safely and effectively.
Screen Analysis
The device screen is turned off. No text, warnings, menus, or values are visible on the screen.
Size and Compatibility
There is an “L” letter on the RESMED AirFit F20 mask box. This indicates that the mask is “Large” size and is designed for users with a facial structure suitable for this size.
Year of Manufacture
The expiration date is stated as 2025-10-27 on the humidifier chamber label. Based on this information, it can be interpreted that the product was manufactured before this date, likely in 2023 or 2024.
Documents
No invoice, warranty certificate, or other documents are visible in the images.
Usage Duration
There is no information regarding usage hours or duration on the device screen, label, or documents.
Existing Faults and Potential Risks
No clear evidence of a fault such as a broken part, error message, disconnected cable, or missing component has been detected in the images. No tangible risk such as severe wear, corrosion, or cable crushing has been observed. The condition of the device and accessories is good.
