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: 27.07.2026
Report code: 1785146667
LÖWENSTEIN MEDICAL LUISA LM150TD Mechanical Ventilator Analysis Report
Device Identification and Brand Model Information
One medical ventilator device has been identified in the images. The device screen is active and displays respiratory parameters. The brand and model information on the label located at the bottom of the device is clearly legible. The brand of the device is determined to be LÖWENSTEIN MEDICAL, and the model is LUISA LM150TD.
Authenticity Assessment
Considering the quality of the label on the product, the CE0197 certification mark, the UDI code, and the general workmanship details, the device is considered to be authentic.
Usage Areas
This device is used to provide life-supporting and non-life-supporting respiratory support for pediatric and adult patients requiring mechanical ventilation. It is suitable for use in home environments, care facilities, hospitals, and mobile applications such as wheelchairs or stretchers. The device can be used for invasive and non-invasive ventilation. Additionally, it features a High Flow Therapy (HFT-Mode) capability.
Quantity Information
There is one main device in the images. No accessories or spare parts belonging to the device are clearly visible in the images.
General Condition and Physical Deformation
The device screen appears to be on and functional. The label is clean and legible. No significant scratches, dents, cracks, discoloration, or dirt have been observed on the device casing, screen, or other visible parts. Its general condition is good.
Mechanical and Electronic Component Inspection
There is no detailed view of the mechanical components in the image. However, no visible issues have been detected on the outer casing. Regarding electronic components, it is observed that the screen is working and displaying all parameters correctly. It is understood that there are some socket inputs at the bottom of the device, but the details are not clear.
Accessories and Battery Status
The box, cables, or other accessories that come with the device are not clearly visible in the images. The battery level is shown as 100% on the device screen, indicating that it has an internal battery and is fully charged.
Detailed Analysis of Label Information
- Serial Number (SN): 50021191. This number is a code that identifies the unique identity of the product and ensures its traceability.
- REF Code: 31410. This code refers to a specific configuration or part number of the product.
- UDI: (01)04050384205967 (21)50021191. The Unique Device Identifier (UDI) is a system used for the global identification and tracking of medical devices.
- Electrical Specifications: 12 V DC max. 7 A, 24 V DC max. 5.4 A, 48 V DC max. 2.7 A. These values indicate the maximum current values at which the device can operate at different voltages.
- + HFT-Mode: Indicates that the device has a High Flow Therapy mode.
- Compliance: Complies with RTCA/DO-160G section 21 category M. This statement indicates that the device complies with certain aviation standards.
- Place of Manufacture: Made in Germany. Indicates that the device was manufactured in Germany.
- CE Mark: CE0197. This mark indicates that the product complies with the European Union’s health, safety, and environmental protection standards.
- IP Code: IP22. This code indicates the level of protection of the device against solid objects and water.
Screen Analysis
The device screen is on and operating actively. Respiratory parameters such as aVCV, VTe (522 ml), PEEP (6.0 hPa), F (18.0 /min), TI (1.20 s), I:E (1:1.8), and MVe (9.1 l/min) are displayed on the left side of the screen. A pressure graph and the current pressure value (20.8 hPa) are located in the middle of the screen. Time (20:33) and date (25.07.2026) information are in the top right corner. The battery level is shown as 100%. The message “Therapy termination” is visible at the bottom of the screen. Functional icons such as home, report, system, light, and lock are also available on the screen.
Dimensions and Compatibility
There is no direct measurement information regarding the physical dimensions of the device in the images. However, the general appearance of the device and its identification as a portable ventilator suggest that it has a compact structure.
Year of Manufacture
The date “2022-11-18” is present on the device label. This date can be accepted as the manufacturing date or labeling date of the product.
Documents
No invoices, warranty certificates, user manuals, or other documents belonging to the device are visible in the images.
Usage Duration
There is no information regarding the usage hours or total operating time on the device screen, label, or any document in the images.
Existing Fault and Potential Fault Risk
No evidence of a significant fault such as a broken part, error message, disconnected cable, or missing component that would prevent the device from operating has been detected in the images. The screen is active and displaying parameters. No condition that would pose a potential fault risk, such as severe wear, rust, or cable crushing, has been observed on the exterior of the device. The general condition of the device is good.
