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: 04.09.2026
Report code: 1788531625
VENTMED DS-7-ST25 BIPAP Device Analysis Report
Device Identification and Basic Information
The examined product is a respiratory device used in the treatment of sleep apnea and respiratory disorders. Based on the labels and screen data in the images, the device has been identified as the VENTMED brand and DS-7-ST25 model. The device consists of a gray main body, a transparent water chamber, a display panel, and control buttons.
- Brand and Model: VENTMED DS-7-ST25
- Device Type: BIPAP Device
- Authenticity: Upon examination of the body quality, label details, screen graphics, and packaging integrity, it is understood that the product is original.
Usage Areas and Compatibility
This device is used for respiratory support therapy for patients with obstructive sleep apnea syndrome, respiratory failure, and similar respiratory tract disorders. It is suitable for use in home environments and clinical settings. It can be used with standard respiratory hoses, masks, and power adapters compatible with the product.
General Condition and Physical Deformation
The general condition of the device is quite new. There is a protective film on the screen. There are no scratches, dents, cracks, color fading, or deformations on the casing surface. There are no visible issues with the mechanical and plastic components.
Electronic Components and Screen Analysis
The electronic components of the device are working properly. When the device is turned on, the VENTMED TECHNOLOGY logo, DS-7-ST25 model, V1.1.005 software version, and Usage Time: 0.8 hours statement appear on the screen. The usage time data here indicates that the device has operated for a total of 0.8 hours.
Accessories and Parts List
The list of parts and accessories identified in the images is as follows:
- 1 VENTMED DS-7-ST25 BIPAP device main body
- 1 black carrying case
- 1 power adapter and cable
- 1 respiratory hose
- 1 thin hose (oxygen or pressure line)
- 1 user manual
- 1 technical label and information sheet
Battery Status and Power Supply
The device does not have an internal battery; it receives its power from the mains electricity via the external power adapter included in the box. There is no crushing, breakage, or deformation on the power adapter cable and socket inputs.
Label and Text Inventory
The texts on the device labels and manual covers are as follows:
- Texts and Codes on the Device: VENTMED TECHNOLOGY, DS-Dream Sleep, power icon, directional buttons, CE 0197, IPX1
- Technical Values on the Label: DS-7 BIPAP Device, LOT number, Feb. 2023 (production date), SN serial number, 24V, 2.5A
- Transport and Operating Conditions: Transport and storage temperature between -20°C and +60°C, operating temperature between 5°C and +35°C, 95% relative humidity limits
- Manufacturer Information: Hunan Ventmed Medical Technology Co., Ltd. The 3rd Floor, Building No.13, Area 1 of Xiangshang Industrial Park, Shaoyang City, 422000, Hunan, P.R. China
- Authorized Representative: Llins Service & Consulting GmbH, Obere Seegasse 34/2, 69124, Heidelberg, Germany
- Importer Information: Medikatek Sağlık Ürünleri ve Hiz. San. Tic. Ltd. Şti., Acıbadem mah. Faik Ali sk. Ersin apt. No:4 K:1 D:2, Kadıköy, İstanbul, 34718, Turkey, Tel: +90 0216 505 56 36
The voltage and current values on the labels indicate the electrical power required for the device to operate, while the temperature and humidity icons indicate the conditions under which the device should be stored and operated. The CE mark indicates the product’s compliance with European standards, and the IPX1 symbol indicates the protection class against water.
Dimensions and Compatibility
There is no numerical information in millimeters regarding the physical dimensions or measurements of the device in the images. The carrying case dimensions and device form are suitable for standard sleep apnea travel and home-use standards.
Production Year
The production date is clearly stated as Feb. 2023 on the technical label of the device.
Documents
Documents containing the user manual and technical information for the device are present in the images. These documents allow the user to safely set up the device, manage menus, and learn maintenance instructions.
Usage Duration
The Usage Time: 0.8 hours data on the device screen shows that the device has operated for a total of 0.8 hours to date.
Existing Faults and Potential Fault Risk
There is no evidence of broken parts, error messages on the screen, broken cables, or any faults in the images. The condition of the device is very good, and no potential fault risk has been observed.
