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: 15.06.2026
Report code: 1781509484
RESMED AutoSet Spirit CPAP Device and Accessories Analysis Report
Device and Accessory Identification
The images contain one RESMED brand AutoSet Spirit model CPAP (Continuous Positive Airway Pressure) device, a carrying case for this device, and one breathing tube. The device is a respiratory support unit used for the treatment of sleep apnea.
Brand and Model Information
The “RESMED” brand is clearly legible on the front face and the bottom label of the device. The “AutoSet Spirit” model is explicitly stated on the front panel of the device. The “RESMED” logo is also present on a metal plate on the front of the carrying case.
Authenticity Assessment
The quality of the logos on the device, the clarity of the label printing, and the general craftsmanship details indicate that the product is an original RESMED manufacture. There are no signs of counterfeiting.
Usage Areas
The RESMED AutoSet Spirit CPAP device is used in the treatment of sleep-related breathing disorders such as obstructive sleep apnea (OSA). The device aims to provide an uninterrupted sleep experience by keeping the patient’s airways open during sleep. It is suitable for use in home and hospital environments. The accompanying breathing tube is a basic accessory used to deliver pressurized air from the device to the patient’s mask.
Quantity Information
- 1 RESMED AutoSet Spirit CPAP device
- 1 RESMED branded carrying case
- 1 breathing tube
General Condition
The device is generally in a used condition. Slight marks due to usage are observed on the outer surface of the device and the carrying case. However, it maintains a solid condition in terms of its general structure.
Physical Deformations
There is slight discoloration and superficial dirt marks on the light-colored upper casing of the device. There is slight yellowing and staining on the transparent label window of the carrying case. No significant scratches, dents, or cracks have been detected on the casing of the device or its accessories.
Mechanical Component Inspection
The buttons on the front panel of the device (up/down arrows, power, and menu buttons) appear to be intact. The hose connection point and power input at the bottom of the device are physically in good condition. The zippers and buckles of the carrying case appear to be functional.
Electronic Component Status
The screen on the front panel of the device is turned off. No error messages or warnings are visible on the screen. The internal status of the device’s electronic components cannot be determined from the images.
Condition of Accessories
The device comes with one dark blue RESMED branded carrying case and one transparent, corrugated breathing tube. There is a metal RESMED logo and a transparent label window on the outer surface of the carrying case. The inside of the case features a “www.resmed.com” address and a world map print. The physical integrity of the tube appears to be intact. The expiration dates of the accessories are not specified in the images.
Battery Status
There is no information in the images regarding whether the device has an internal or external battery, nor any clues about the physical condition of a battery.
Label Information and Explanations
- Serial Number: 20030104010460. This number is the unique identification number the device has had since production. It is used for product tracking, warranty processes, and service history.
- REF Code: 36207. This code is the catalog or reference number of the product. It ensures that the product is correctly identified and ordered.
- CE Mark: Indicates that the product complies with the European Union’s health, safety, and environmental protection standards.
- 0120: This four-digit number used with the CE mark is the identification number of the notified body that assessed the product’s conformity.
- TGA AUST L 43136: This is the listing number issued by the Australian Therapeutic Goods Administration (TGA). It indicates that the product can be legally sold in the Australian market.
- 100-240V, 2.2A, 50-60Hz: Specifies the electrical supply requirements for the device to operate. It indicates that it can operate within a wide voltage range (universal).
- “Federal (USA only) law restricts this device to sale by or on order of a physician.”: This statement is a legal warning indicating that the device can only be sold by or on the order of a physician in the United States.
Screen Analysis
The screen on the front panel of the device is turned off. Therefore, no text, menu, warning message, or value analysis can be performed on the screen.
Dimensions and Compatibility
There is no specific information in the images regarding the exact dimensions of the device or user compatibility. However, the fact that the device is presented with a carrying case suggests that it has a compact and portable structure. This indicates that the device can be easily transported for travel as well as home use.
Year of Manufacture
There is no direct information regarding the year of manufacture on the bottom label of the device. However, the first four digits of the serial number are read as “2003”. According to the serial number format of ResMed devices, the third and fourth digits usually indicate the year of manufacture. Based on this information, it can be interpreted that the device may have been manufactured in 2003.
Documents
There are no invoices, warranty certificates, user manuals, or other official documents belonging to the device in the images.
Usage Duration
No information indicating the total usage duration (e.g., operating hours) of the device has been encountered on the screen, label, or in the images.
Existing Faults
No concrete evidence of a fault such as a broken part, error message, severed cable, or missing component that would prevent the device from operating has been detected in the images.
Potential Risk of Failure
No obvious conditions that could pose a potential risk of failure, such as severe wear, rust, or cable crushing, have been observed in the general condition of the device and its accessories. The slight discoloration and dirt on the outer casing of the device do not pose a risk that would affect its functionality.
