Defective Secondhand Bıçakçılar 175S Suction Device

Objective AI Report

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Report date: 07.12.2025

Bıçakcılar Surgical Aspirator Device Analysis Report

Device Identification

The product in the image is a mobile surgical aspirator (vacuum) device used for medical purposes. It features a wheeled metal body, a carrying handle, an analog pressure gauge, and a vacuum adjustment knob. The device is professional medical equipment designed for the aspiration of body fluids.

Brand and Model

During a detailed visual inspection, the embossed BIÇAKCILAR brand logo is clearly visible on the metal front panel of the device. The name BIÇAKCILAR is also present inside the pressure gauge (manometer). The manufacturer of the manometer is the PAKKENS brand, as indicated by the logo on its dial. Since there is no directly readable label for a model name (e.g., “Vaculine” or a specific numerical code) in the images, model information is not specified.

Originality

The device’s body design, the embossed brand craftsmanship on the metal, the presence of original labels, and the use of a specially manufactured manometer with the Bıçakcılar logo confirm that the product is an original Bıçakcılar production.

Areas of Use

This device is used in medical environments such as operating rooms, emergency departments, and intensive care units; during surgical operations or patient care to vacuum and clear (aspirate) blood, mucus, and other body fluids. Its portable nature makes it suitable for inter-departmental transfer within the hospital.

Quantity Information

The images show 1 unit of the surgical aspirator main unit. The jars and connection hoses that need to be attached to the device are not present in the image.

General Condition and Cosmetics

The device is in a used condition. It is second-hand. There are signs of use on the gray painted parts of the body. Especially on the top cover surface and around the carrying handle, dulling and superficial stains are observed, which are thought to be due to liquid contact or cleaning agents.

Physical Deformation

No significant dents, dings, or deep rust that would affect the general operation have been detected on the device’s outer metal casing. The blue front panel is clean. Only cosmetic stains on the top surface and dullness in the paint surface, developed over time, are present.

Mechanical and Hardware Analysis

• Wheels: There are 4 wheels at the base of the device. The wheels appear visually sound and support the device’s mobile feature.
• Carrying Handle: A robust, integrated carrying handle is present on the upper part of the device.
• Side Rails: On both sides of the device, there are metal rails used for hanging aspiration jars (collection containers). These rails appear physically intact but are empty.
• Control Knob: At the bottom, there is a black, rotary-type vacuum adjustment knob (regulator). No physical damage is visible on the knob.

Electronic and Indicator Analysis

• Pressure Gauge (Manometer): An analog vacuum gauge is located in the center of the front panel. The gauge scale ranges from 0 to 760 mmHg (millimeters of mercury). Its glass is intact and appears crack-free.
• Signal Lamp: Directly below the manometer, there is a green signal lamp (likely a power on/off indicator).
• Power Connection: An electrical cable connected to the device is not fully displayed in the image; it is likely at the rear or not attached.

Label and Warning Information

On the upper part of the device, behind the carrying handle, a white information label contains warning texts in Turkish and English:

• Warning Content: A vital warning note regarding the use and maintenance of the hydrophobic filter is partially legible, stating: “DİKKAT! … HİDROFOBİK FİLTRENİN … TIKANMASI ASPİRASYON İŞLEMİNİ DURDURUR, FİLTREYİ DEĞİŞTİRİN.” (CAUTION! … CLOGGING OF THE HYDROPHOBIC FILTER … STOPS THE ASPIRATION PROCESS, REPLACE THE FILTER.)

Missing Parts (Accessories)

The following parts, which are necessary for the device to be functionally usable, are not present in the image:

• Collection jars (Aspiration jars).
• Patient-to-device connection hoses.
• Hydrophobic filter (No filter is attached to the hose inlet at the top).

Current Fault and Risk Assessment

Visual inspection does not reveal concrete evidence (such as broken parts, severed cables, etc.) indicating that the device is non-functional or faulty. However, the absence of collection jars suggests that the device is not immediately ready for use. Since the stains on the upper part indicate intensive use, it is recommended to test the motor performance and vacuum power. Its physical integrity has been preserved.