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: 16.07.2026
Report code: 1784184484
LOWENSTEIN Medical WM 090 TD Respiratory Support Device Analysis Report
Device and Accessory Identification
The images show a respiratory support device used in the treatment of respiratory conditions such as sleep apnea, along with its accessories. Components such as the main device, carrying case, power adapter, breathing tube, and nasal mask have been identified.
Brand and Model Information
The LOWENSTEIN medical brand is clearly visible on the device and the carrying case. The label on the bottom of the device specifies the model as WM 090 TD.
Authenticity Assessment
Upon examining the LOWENSTEIN medical logo on the device, the print quality of the labels, and the general craftsmanship details, the impression is that the product is original. The CE mark and manufacturer information also support this assessment.
Usage Areas
This device is a pressure-controlled, non-invasive therapy device used in the treatment of sleep apnea and other sleep-related respiratory disorders. It provides respiratory support by delivering positive airway pressure to patients. The nasal mask in the image indicates that the device is used to provide therapy via the respiratory tract.
Quantity Information
- Main Device: 1 unit
- Carrying Case: 1 unit
- Power Adapter: 1 unit
- Breathing Tube: 1 unit
- Nasal Mask (in package): 1 unit
General Condition and Physical Deformation
The general condition of the device is considered used. There are no visible scratches, dents, or cracks on the casing. There is slight dust on the surfaces. Slight wear and dust due to usage have also been observed on the carrying case.
Mechanical and Electronic Component Inspection
The control buttons and connection points on the side of the device appear to be intact. No visible wear or damage has been detected on the breathing tube. The internal electronic components of the device are not visible in the images; therefore, no comments can be made regarding the internal components. From an external perspective, there are no issues that would affect the functionality of the electronic components.
Accessories and Connection Points
The device comes with a carrying case bearing the LOWENSTEIN medical logo, a power adapter, and a breathing tube. Additionally, a PHILIPS Respironics branded nasal mask in its packaging is included among the accessories. On the left side of the device, there is a connection point for the breathing tube and an input for the power adapter. All accessories appear to be complete. There is no information regarding the expiration dates of the accessories in the images.
Battery Status
There is no information in the images regarding an internal or external battery for the device, nor any details about the physical condition of a battery. It is understood that the device operates via a power adapter.
Label Information and Meanings
- Serial Number (SN): T1230719. This number is a code that identifies the unique identity of the product and ensures its traceability.
- Model Type (TYP): WM 090 TD. Defines the specific model and technical specifications of the device.
- Operating Voltage: 24V —. Specifies the electrical voltage required for the device to operate correctly.
- CE Mark: CE0197. Indicates that the product complies with the European Union’s health, safety, and environmental protection standards. “0197” is the identification number of the notified body.
- Compliant Standard: Complies with RTCA/DO-160G section 21, category M. This statement indicates that the device complies with a specific section of the standard for environmental conditions and test procedures for airborne equipment.
- Manufacturer Information: Lowenstein Medical Technology GmbH + Co.KG, Kronsaalsweg 40, 22525 Hamburg, Germany. Shows the manufacturer and address of the device.
- Ingress Protection Rating (IP): IP21. Specifies the level of protection against solid objects (2: fingers, etc.) and water (1: vertically dripping water).
- Manufacturing Date: 2021-09. Indicates that the device was manufactured in September 2021.
- Support Line: SAPIO 24/7 SUPPORT LINE (0212) 452 87 37. This information is the contact number for the local support or service provider of the device.
Screen Analysis
The device screen is either off or not clearly visible in the images. Therefore, no analysis could be performed regarding any text, warnings, menus, or values on the screen. Only the control buttons were observed.
Dimensions and Compatibility
There is no direct information in the images regarding the exact dimensions of the device or its compatibility with user body sizes. However, the compact structure of the device and the fact that it is presented with a carrying case suggest that it is a portable respiratory support device.
Year of Manufacture
The “2021-09” marking is clearly visible on the label on the side of the device. This information indicates that the device was manufactured in September 2021.
Documents
There are no official documents directly related to the product, such as an invoice, warranty certificate, or user manual, in the images. Only a business card or promotional card belonging to the “Fen Medikal” company is visible. This card does not provide any additional benefit to the buyer.
Usage Duration
No information regarding usage hours or total duration of use was detected on the device screen, labels, or any documents in the images. This data could be important for understanding the intensity of the device’s past usage, but it could not be obtained from the images.
Existing Faults
As a result of a detailed examination of the images, no evidence of a clear fault such as a broken part, error message, severed cable, or missing component was detected on the device. The physical integrity of the device appears to be maintained.
Potential Risk of Failure
The general condition of the device is good. No concrete situation that could pose a potential risk of failure, such as severe wear, rust, or cable crushing, was observed in the images. Based on its external appearance, it is assessed that the device does not carry any immediate risk of failure.
