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: 02.06.2026
Report code: 1780404385
LOWENSTEIN LUISA LM150TD Ventilator Analysis Report
Device and Accessory Identification
The images show one LOWENSTEIN LUISA LM150TD model ventilator, one power adapter, one breathing circuit, and one carrying case. The device is a medical ventilator designed to provide respiratory support.
Brand and Model Information
- Ventilator Brand-Model: LOWENSTEIN LUISA LM150TD
The “LOWENSTEIN medical” logo and the “LUISA” inscription are clearly legible on the front of the device. The label on the bottom of the device clearly indicates the model information “LUISA LM150TD” and the manufacturer information “LOWENSTEIN Medical Technology GmbH + Co. KG”.
Authenticity Assessment
The brand logo, model label, and technical information on the device suggest that the product is authentic. The CE0197 mark on the label indicates the product’s compliance with European standards.
Usage Areas
This device is a ventilator designed for life-supporting and non-life-supporting ventilation of 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. It can be used in invasive and non-invasive ventilation modes. The “HFT-Mode” (High Flow Therapy) feature indicated on the label shows that the device can provide high-flow oxygen therapy.
Quantity Information
- Ventilator Device: 1 unit
- Power Adapter: 1 unit
- Breathing Circuit: 1 unit
- Carrying Case: 1 unit
General Condition and Physical Deformation
The general condition of the device is used, with dust and visible scratches on the screen surface. There is no visible major deformation on the device casing other than slight dust. A white label with the text “HASTAYA AİTTİR” (BELONGS TO PATIENT) and another label with a barcode are affixed to the front.
Mechanical and Electronic Components
The power button and other buttons on the front panel of the device appear to be intact. The carrying handle or grip of the device also shows no signs of damage. No significant issues were detected in the externally visible parts of the electronic components. Since the screen is off, there is no visual information regarding the status of the internal electronic components.
Condition of Accessories
- Power Adapter: It is a black HP brand adapter. The cables are disorganized.
- Breathing Circuit: It is a transparent, corrugated hose. It is wrapped with a blue band. No wear or breakage is visible.
- Carrying Case: It is a black, zippered carrying case. It is used to transport the device and accessories.
Since the back or side parts of the device are not clearly visible, a detailed analysis of the socket inputs cannot be performed. There is no expiration date information on the accessories.
Battery Status
There is no information or image regarding the internal or external battery of the device in the images. Therefore, no comment can be made about the battery status.
Label Information
- UDI: (01)040400384290987 (21)50021250
- Model: LUISA LM150TD
- REF Code: 31410
- Voltage and Current Information:
- 12 V DC max. 7 A
- 24 V DC max. 3.4 A
- 40 V DC max. 2.7 A
- Mode: + HFT-Mode
- Place of Manufacture: Made in Germany
- CE Mark: CE0197
- Serial Number (SN): 50021250
- Date: 2023-11-21
- Other Symbols: WEEE (Waste Electrical and Electronic Equipment) symbol, symbol indicating it is not for single use, symbol to refer to the user manual, MD (Medical Device), and IP22 (Ingress Protection) classification.
- Additional Label: SAFO life
UDI (Unique Device Identifier): A system that enables the global identification of medical devices. These codes improve the tracking and safety of the device.
REF Code: The reference or catalog number of the product. This code identifies a specific product variant or configuration.
Voltage and Current Information: Shows the maximum current values at which the device can operate at different DC voltage inputs. This information is important for selecting the correct power supply.
HFT-Mode: Indicates that the device supports the High Flow Therapy mode.
CE Mark: Indicates that the product complies with the European Union’s health, safety, and environmental protection standards.
Serial Number (SN): A unique identification number for each device. It is used for device tracking, warranty processes, and service history.
2023-11-21 Date: This date may be the label printing date, the final inspection date, or the packaging date of the device. It provides a clue about the year of manufacture.
WEEE Symbol: Indicates that electronic waste must be collected separately.
MD IP22: Indicates that the device is a medical device and has an IP22 protection class. IP22 means that the device is protected against solid objects to a certain level and vertically falling water drops.
The label with the text “HASTAYA AİTTİR” and the barcode label on the front of the device indicate that the device has been assigned to a patient and is likely tracked by a healthcare institution. The “06/11/2023” date on the barcode label may be the date the device was delivered to the patient or registered.
Screen Analysis
The device screen is off. No text, menu, warning message, or value is visible on the screen. There is dust and visible scratching on the screen surface.
Dimensions and Compatibility
There is no numerical information about the exact dimensions or size of the device in the images. However, the compact structure of the device and its presentation with a carrying case suggest that it is a portable ventilator suitable for mobile use.
Year of Manufacture
There is no direct year of manufacture information on the bottom label of the device. However, there is a “2023-11-21” date on the label. This date is a concrete clue indicating that the device was manufactured no later than 2023 or underwent a quality control/labeling process on this date. Therefore, it can be interpreted that the production period of the device is 2023 or earlier.
Documents
No invoice, warranty certificate, user manual, or other documents belonging to the device are visible in the images.
Usage Duration
Since the device screen is off, no visual information regarding the total usage hours or duration can be obtained. There is no mention of this information on the labels either.
Existing Fault
No clear evidence of a fault, such as a broken part, error message, or disconnected cable that would prevent the device from operating, has been detected in the images. There are no signs of a serious functional failure other than scratches and dust on the screen surface.
Potential Risk of Failure
The general condition of the device is good, apart from superficial scratches and dust on the screen. No concrete situation that could pose a potential risk of failure, such as serious wear, corrosion, or cable crushing, has been observed.
