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: 01.04.2026
Report code: 1775025135
VENTIlogic LS Mechanical Ventilator Analysis Report
Device Identification and Usage Areas
The product in the images is a mechanical ventilator device used to provide respiratory support. As understood from the menus and buttons on the device, it is used for patients requiring pressure-supported ventilation. The device is equipped with hardware that supports respiratory modes such as IPAP, PEEP, and SIMV.
Brand and Model Information
The VENTIlogic LS inscription is clearly visible on the front panel and the information screen of the device. The device is identified by this model name.
Authenticity Assessment
Upon examination of the device’s casing craftsmanship, screen resolution, menu interface design, and the print quality of the information labels, it is assessed that the product is an original medical device.
Quantity Information
There is 1 main device in the images. No external hoses, masks, or power cables connected to the device are visible.
Physical Condition
The device is in used condition. There is slight superficial dust accumulation on the outer casing due to usage, but no breaks, cracks, deep scratches, or dents have been observed. The overall physical condition of the device is good.
Mechanical and Electronic Components
The carrying handle on the top of the device appears sturdy. The membrane keypad on the front panel and the adjustment knob on the bottom right corner are physically undamaged. The air outlet port located on the bottom left is intact. Electronically, it is observed that the device is operational, with the screen backlight and the notification LED lights on the panel active.
Screen and Software Analysis
The device’s color LCD screen is functioning properly. There are no dead pixels or darkening on the screen. The data obtained from the screen is listed below.
- The software version is stated as 3.13.3.
- The date 30.11.2022 is located next to the software version.
- The active operating mode of the device is set to SIMV Prog. 1.
- The inscription Double hose valve is present on the screen.
- Respiratory parameters are set as PSIMV 25.0 hPa, IPAP 25.0 hPa, and PEEP 5.0 hPa.
- There is an icon on the screen indicating that an SD card is inserted.
Battery Status
There are two battery icons in the top right corner of the device’s operating screen. While the first battery icon appears yellow and full, the second battery icon is red and has a cross mark on it. This indicates that a second battery is missing, faulty, or completely discharged.
Label and Warning Information
Maintenance and usage conditions are specified on the information label located on the top casing of the device. The information read from the label is as follows:
- It states that certain parts must be replaced every 1000 hours within the scope of the maintenance period.
- It is stated that the dust filter should be cleaned weekly and replaced every 6 months.
- Charging instructions for users and dealers are provided under the battery usage conditions heading.
- There is a warning label on the air outlet port containing the diameter information of 15mm – 22mm.
Dimensions and Compatibility
The 15mm – 22mm inscription on the air outlet port indicates that the device is compatible with standard medical respiratory circuits. These measurements suggest that the device can be used for both adult and pediatric patients by using appropriate hoses.
Usage Duration and Production Year
The total operating time is clearly stated as 3614.66 h on the device’s information screen. Although there is no clear production year label in the images, the software version date of 2022 indicates that the device was produced on or before this date.
Fault and Risk Assessment
There is no fault or damage to the physical integrity of the device. The red LED light on the operating screen and the red battery icon with a cross mark indicate that there is a battery issue or an alarm is active due to it not being connected to a patient. Apart from this, no physical wear that would pose a potential fault risk has been observed on the casing or ports. The overall mechanical condition of the device is good.
