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: 30.07.2026
Report code: 1785398544
BİÇAKCILAR VACULINE MAXI-E Surgical Aspirator Analysis Report
Device Identification and Brand Model Information
One surgical aspirator device has been identified in the images. The device is a vacuum unit designed for the aspiration of fluids and particles during medical procedures. The brand and model information on the label located on the rear panel of the device is clearly legible.
- Brand: BİÇAKCILAR
- Model: VACULINE MAXI-E SURGICAL ASPIRATOR
Authenticity Assessment
Upon examining the BİÇAKCILAR logo, CE mark, and other label information on the device, as well as the print quality and general craftsmanship details, the impression is that the product is original. The labels and the general structure of the device reflect professional manufacturing quality.
Areas of Use
The BİÇAKCILAR VACULINE MAXI-E surgical aspirator is used in hospitals, clinics, operating rooms, and emergency services for surgical operations, endoscopic procedures, clearing respiratory tract secretions, and other medical aspiration needs. Thanks to its high vacuum and high flow rate features, it is suitable for effective use in various medical branches.
Quantity Information
The images show one main surgical aspirator device, one collection jar, and one external cylindrical filter or additional collection container. The device’s power cable is also included among the accessories.
General Condition and Physical Deformation
The general condition of the device appears to be good. No significant scratches, dents, cracks, or discoloration have been detected on the casing. Slight dust accumulation may be visible on the surfaces, but this does not negatively affect the condition of the device.
Mechanical and Electronic Component Inspection
The analog vacuum gauge and adjustment knob on the top panel of the device appear to be intact. No breakage or deformation has been observed in the mechanical components such as the wheels and the carrying handle of the device. The power input and fuse slots on the rear panel are intact. The internal structure of the electronic components is not visible in the image, but no issues have been detected at the external connection points.
Accessories and Connection Points
A collection jar and connection hoses are provided with the device. There is also another cylindrical, transparent accessory on the side of the device. The power cable is wrapped around the cable holder on the back of the device, and the plug is intact. There are two fuse inputs and one power cable input on the rear panel of the device. All socket inputs appear clean and intact.
Battery Status
No internal or external battery belonging to the device has been detected in the images. It is understood that the device operates directly on mains electricity.
Label Information
The label on the rear panel of the device contains the following information:
- Serial Number (SN): 795
- Year of Manufacture: 2019-09 (September 2019)
- Voltage (VAC): 230
- Frequency (Hz): 50/60
- IP Code: X1
- Power (W): 145
- Reference Code (REF): M4E 650 0 0
- Fuse Information: F3.15L, 250V (5x20mm)
- CE Mark: CE0044
The Serial Number (SN) is the unique identification number of the device and ensures its traceability. The Year of Manufacture indicates when the device was produced. Voltage (VAC) specifies the alternating current voltage required for the device to operate. Frequency (Hz) indicates the frequency of the electrical grid. The IP Code expresses the degree of protection of the device against solid objects and water. Power (W) indicates the electrical power consumed by the device during operation. The Reference Code (REF) is the model or catalog number of the product. Fuse Information shows the type and value of the fuses that protect the device’s electrical circuit from overcurrent. The CE Mark indicates that the product complies with European Union health, safety, and environmental protection standards.
Screen Analysis
The device does not have a digital screen. Instead, there is an analog manometer that shows the vacuum level. The values on the manometer range from 0 to 760 mmHg, and the needle is resting at approximately 0 mmHg. The gauge glass is clean and legible.
Dimensions and Compatibility
There is no direct information regarding the exact measurements or size of the device in the images. However, its wheeled and vertical structure suggests that it is of standard surgical aspirator dimensions. It has a design suitable for general use in a medical environment.
Year of Manufacture
The year of manufacture is clearly stated as “2019-09” on the label on the rear panel of the device. This information indicates that the device was manufactured in September 2019.
Documents
No invoices, warranty certificates, user manuals, or other documents belonging to the device are visible in the images.
Usage Duration
No information regarding the total usage hours or duration has been detected on the device or its labels.
Existing Fault
There is no clear evidence of a fault in the images, such as a broken part, error message, severed cable, or missing component that would prevent the device from operating.
Potential Fault Risk
The general condition of the device is good. No concrete situation that could pose a potential fault risk, such as severe wear, rusting, or cable crushing, has been observed in the images.
