Objective AI Report
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Report date: 23.02.2026
ELIT SL-F601 Anti-Decubitus Air Mattress System Analysis Report
Device Identification
The product examined in the visuals is a motorized (compressor-equipped) air mattress system designed to prevent the formation of pressure sores (decubitus) in bedridden patients and to aid in the healing of existing wounds. The system consists of a main control unit (pump) that manages air pressure and an air-channeled mattress on which the patient lies. The product is a medical treatment and care support device.
Brand and Model Information
During the detailed visual inspection, the brand and model information was clearly identified on the device’s front panel and the top surface of the mattress.
- Brand: ELIT
- Model: SL-F601
- Product Description: ANTI-DECUBITUS SL MATTRESS SERIES
- Manufacturer: BEIJING SHENLU MEDICAL DEVICE CO., LTD
Areas of Use
This system is used in patients who must lie down for extended periods to relieve blood circulation by reducing pressure on tissues and to prevent the formation of bedsores. It is suitable for use in intensive care units, palliative care centers, and for paralyzed or bedridden patients requiring home care. As understood from the “Turn” buttons and indicators on it, the SL-F601 model has the ability to position the patient left-right (rotation).
Quantity and Component Information
The overall set integrity in the visuals is as follows:
- 1 ELIT brand control unit (Air pump/compressor).
- 1 blue-colored mattress with air cells.
- Multi-air hose assembly connecting the control unit to the mattress (Blue, orange, and yellow colored hose group).
- Integrated power cable.
General Condition and Physical State
According to the label data, the product was manufactured in 2021 and is a used device. Its physical integrity has been preserved. The mattress shows normal creases due to use and folding, but there is no visual data indicating tears or punctures. The external casing of the pump unit has slight signs of use, stains, and dust accumulation on the plastic surface due to its shelf life. No serious cracks or fractures have been observed.
Front Panel and Control Functions Analysis
Upon examining the device’s front panel, the following control mechanisms and functions were identified:
- Pressure Adjustment: A manual pressure adjustment knob (potentiometer) with “Soft and Hard” markings and an increasing scale from left to right is present. The knob is grey and mechanically in place.
- Mode Buttons: There are three physical buttons on the panel: “Supine”, “Turn”, and “Alarm Stop”.
- LED Indicators: Green illuminated indicator areas displaying the device’s status are present: “Supine”, “Low Turn”, “Medium Turn”, “High Turn”. Additionally, there is a red square warning area designated for “Alarm”.
- Language Option: All instructions on the panel (Soft, Hard, Supine, Turn, etc.) are in Turkish.
Label and Technical Data
The silver-colored manufacturer’s label on the back of the device is legible and contains the following technical data:
- Voltage: AC220V ± 22
- Input Power: 15W
- Frequency: 50Hz
- Pressure: ≥ 8Kpa
- Flow Rate (Air Flow): ≥ 6L/min (6 liters per minute and above)
- Noise Level: ≤ 40dB
- Fuse: 250V 0.2A
- ID No: 0212F0501127
- CE Certificate No: 02223
- Ref Standard: The Ref code is not additionally specified in the visual, but the brand model SL-F601 is the reference.
Year of Manufacture and Origin
According to the data on the label, the device’s production date is 2021.05.01. The product’s origin is the People’s Republic of China (Made in China). The importer company is stated as “Okyanus medical Saglik urunleri tic. Ltd. Sti.”.
Accessories and Connection Points
The black power cable extending from the left side of the device maintains its integrity. The air hose group emerging from the front-left side has color-coded (blue, orange) inlets, and the hoses pass through a green protective sleeve (organizer). No kinking or breakage of the hoses is observed at the pump inlet. At the foot end of the mattress, white printed graphics (footprint icons) indicating foot position are present.
Mechanical and Rear Design
On the rear part of the pump, there are integrated grey plastic hanger brackets (hook structure) for suspending the device on a patient’s bed frame. No visible deformation or cracks are present on the hanger brackets.
Potential Failure Risk Assessment
During the visual inspection, no critical damage (casing crack, broken cable, crushed hose) that would prevent the device from operating was identified. However, considering the possibility of hose inlets (sockets) leaking air over time and slight dirt on the plastic components, it is recommended to perform an air leak test before starting use. Given the device’s age (approximately 5 years), checking the compressor performance (pressure generation) would be appropriate. The device, in its current state, appears to be in a “may require maintenance but is a candidate for operation” condition.
