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: 18.08.2026
Report code: 1787050825
Liko Viking Mobile Lift System Analysis Report
Device Identification and Basic Information
The product examined in the images is a mobile lift system used for patient transfer and lifting operations. The main body of the product, its wheeled chassis, lifting arm, and suspension apparatus are visible in the images. Promotional and technical specification brochures belonging to the Liko brand are also included in the visual inventory. This device, which falls under the patient transport lift category, is designed to safely lift a patient from a bed or wheelchair and transport them to a different location.
Brand and Model Information
The brand name Liko is visible on the brochures and labels on the device. The Viking series is listed as the model name in the brochures, which include the Viking XS, Viking S, Viking M, Viking L, and Viking XL options. Details regarding this model series are clearly stated on the parts of the device and in the brochure texts.
Authenticity Assessment
Based on the examination of the product’s body design, logo quality on the brochures, safety warnings, and standard symbols, it is understood to be an original medical device. The CE and international safety certification marks present on the device support its original structure.
Usage Areas
This device enables the safe transfer of patients with physical limitations between beds, wheelchairs, toilets, or bathtubs without physical strain. It is widely used in hospitals, nursing homes, and home care services. It facilitates the daily care processes for patients who have lost the ability to walk or have difficulty standing.
Quantity Information
The images show 1 main mobile lift body and informational brochures belonging to the device. No extra spare parts or accessories were counted.
General Status and Condition
The main body and parts of the device are protected by being wrapped in stretch film. In the photo taken outdoors or in a storage area, the metallic frame of the device is seen fully wrapped. The brochure papers are in clean and readable condition.
Physical Deformation
Due to the protective packaging materials covering the outer surface of the device, the direct surface of the metal components is not clearly visible. No clear fractures or dents were detected on the wheeled lower chassis and the wrapped parts visible in the image.
Mechanical Components
Mechanical components, including the wheels, base expansion mechanism, and lifting arm hinges, are packaged. No mechanical breakage or missing parts were observed in the images.
Electronic Components
In the images, the electronic motor, battery box, and control parts are in a closed position under the stretch film. The connection cable and keypad of the controller are detailed in the brochure images, and these components are positioned on the main device wrapped in packaging.
Accessories and Connection Ports
The device comes with a green-colored sling used to carry the patient and a handheld control unit. Since the socket inputs on the device remain under the packaging, they could not be counted directly from the image; however, the brochure information states that it includes a remote control and a battery system with a charge indicator. There is no indication regarding the expiration dates of the accessories.
Battery Status
There is an internal or external battery box on the device; however, the capacity or physical condition (swelling, leakage, etc.) of the battery cannot be directly analyzed due to the closed packaging and the distance at which the image was taken. The brochure states that an eco-friendly NiMH battery is used.
Label and Text Inventory
The texts appearing on the brochures and the device in the images are as follows: Liko, New Generation Mobile Lift Systems, Important Features, Viking, Hill-Rom, Enhancing Outcomes for Patients and Their Caregivers, Universal Medikal Araçlar San. ve Tic. Ltd. Şti., www.hill-rom.com, www.liko.com, CE, EMC, ETL, ISO 9001, ISO 13485, ISO 14001, MDD 93/42/EEC, IEC 60601-1, IEC 60601-1-2, SS-EN ISO 10535, UL-60601-1, CAN/CSA C22.2 No. 60601.1, Design and Quality by Liko in Sweden, Doc No: 7R135305-01, Design: Hill-Rom Marketing Communications, 2012-04. These texts verify the production standards of the device, contact information for the authorized distributor, the international safety norms it complies with, and technical manual reference numbers.
Screen Analysis
There is no digital screen on the device. Physical buttons are located on the control box and the hand controller instead of a screen.
Dimensions and Compatibility
According to the table in the brochure, the dimensions and capacity values of the Viking series are as follows: For the Viking XS model, maximum load is 160 kg, weight is 25 kg, maximum lifting height is 155 cm; for the Viking S model, maximum load is 160 kg, weight is 25 kg, maximum lifting height is 175 cm; for the Viking M model, maximum load is 205 kg, weight is 34 kg, maximum lifting height is 179 cm; for the Viking L model, maximum load is 250 kg, weight is 40 kg, maximum lifting height is 179 cm; for the Viking XL model, maximum load is 300 kg, weight is 42 kg, maximum lifting height is 187 cm. This data allows for the selection of the appropriate model according to the patient’s height and weight.
Production Year
The 2012-04 notation at the end of the document code in the brochure documents indicates the printing period of the document and design. Although the physical label on the body of the device is not directly readable, it carries periodic traces from the brochure data.
Documents
The images include promotional brochures containing the product’s technical specifications, capacity tables, safety standards, and information about the authorized distributor in Turkey (Universal Medikal Araçlar San. ve Tic. Ltd. Şti.). These documents guide the buyer regarding the technical limits and compliance certificates of the device.
Usage Duration
There is no counter or digital data in the images showing the total operating hours or usage duration of the device.
Existing Faults
Due to the main body of the device being wrapped in stretch film in the images, there is no clear evidence of a mechanical or physical fault. No broken parts or error messages were detected.
Potential Fault Risk
A deep risk analysis cannot be performed because the outer surface of the device is wrapped in protective packaging. As observed from the image, the metal frame is in good condition, and there is no visible risk of concrete rusting or cable crushing.
