Objective AI Report
Disclaimer: I am Medbidding AI. I am an unbiased AI agent. 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: 26.10.2026
Report code: 1793011230
Löwenstein prisma SMART Sleep Apnea Device Analysis Report
Device Identification and Basic Information
The images show a positive airway pressure device used in the treatment of respiratory tract disorders. The main body of the device is made of dark-colored plastic, and the front surface features control buttons and a display panel. The product comes with a carrying case, power adapter, breathing tube, mask, and spare filters.
Brand and Model
The Löwenstein medical brand is written in white on the front left panel of the device and on the carrying case, while the prisma SMART model name is located above the power button. The model name has been transferred to the report while maintaining the letter and number sequence.
Authenticity and Condition Assessment
The details observed on the device body, logos, and label prints indicate that the material meets original standards. The device is generally in clean condition, and there are no visible deep scratches, cracks, dents, or discoloration on its outer surface.
Usage Areas and Compatibility
This device is used to provide respiratory therapy to keep the airways open for patients experiencing respiratory arrest during sleep. It is structured to be suitable for the respiratory support processes of individuals undergoing sleep apnea treatment in a home environment. It forms a complete set with the included standard tube, mask, and adapter components and is suitable for immediate use.
Quantity Information
The total inventory of products and accessories in the images is as follows: 1 main device, 1 carrying case, 1 power adapter and cable, 1 breathing tube, 1 mask, and 2 black sponge filters in a transparent bag.
Mechanical and Electronic Components
The power, minus, plus, and menu buttons on the front panel of the device are mechanically in place. The tube outlet port and side cover mechanisms function without issues. The electronic display panel and the integrated circuit parts under the keypad appear intact in the image; there are no signs of burns or broken wires.
Accessories and Connection Ports
The device comes with a black fabric zippered carrying case, a power adapter providing mains connection, a gray-colored tube that delivers respiratory circuits to the patient, and a mask with a head strap. Additionally, there are 2 air filters with the code REF WM 29928 inside a transparent sealed bag. The air outlet port on the left side of the device and the adapter socket input on the back are clean and in usable condition.
Battery Status
There is no visible slot, label, or external battery unit for the device’s internal battery in the images; the device operates directly via the mains adapter.
Label and Text Inventory
Various technical texts and codes can be read on the rear label of the device and on the accessory packaging. The label on the back of the device contains BN 602100 and a 2022-12 date stamp. Labels containing the Sapio Life 24/7 support line phone number and instruction icons are affixed to the device. The power adapter cable features the text H05VVH2-F 2XO.75mm2 and BAOHING, along with KEMA-KEUR standard symbols. The label on the filter bag contains REF WM 29928, the number 4 050384 251587 under the barcode, the code WM 77091e, the address of Löwenstein Medical Technology GmbH+Co.KG, and the date 2022-12. These texts allow for the verification of the product’s manufacturing information, serial references, safety standards, and authorized contact lines.
Display Analysis
The display panel on the front surface of the device is black and turned off; no menu text or warning icons are visible on the screen.
Dimensions and Compatibility
The images do not contain the millimetric measurements or weight values of the device. It is understood from the proportions in the image that the device is of standard home-type respiratory device dimensions.
Manufacturing Year
The 2022-12 markings on the rear label of the device and on the filter bag indicate that the product was manufactured in December 2022.
Documents
There is no invoice, printed warranty certificate, or user manual booklet in the images.
Usage Duration
Since the device screen is off and there is no counter data on the labels indicating operating hours, there is no information in the image regarding the total operating time of the device.
Existing Faults and Potential Risk of Failure
Visual inspection reveals no evidence of existing faults such as broken parts, dents, broken cables, or error messages on the device casing, tube, or adapter cables. The general condition of the device is good; no significant wear or corrosion has been observed on the cables.
