Secondhand Nüve OT 4060V 75 Liters Autoclave

Objective AI Report

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Report date: 27.03.2026
Report code: 1774605970

Nüve OT 4060V Autoclave Device Analysis Report

Device Identification and Basic Information

The product shown in the images is a top-loading, vertical steam sterilizer (autoclave) device. The primary purpose of the device is to ensure the sterilization of medical instruments, laboratory materials, or textile products using high pressure and steam.

• Brand and Model: Nüve OT 4060V
• Quantity: 1 main unit
• Authenticity: The logo on the control panel, the brand markings on the manometer dials, and the overall industrial design indicate that the device is original.

Areas of Use

This device is suitable for use in hospitals, dental clinics, veterinary clinics, research laboratories, and microbiology laboratories for the sterilization of surgical instruments, glass materials, and liquids.

Physical Condition and State

The device is in used condition. General dust accumulation, staining, and superficial signs of use are present on the stainless steel outer casing. No deep scratches, dents, dings, or rust that would compromise the integrity of the device have been observed on the body panels. The overall physical condition of the device appears sound.

Mechanical Component Analysis

The dome-shaped stainless steel lid located on the upper part of the device and the multi-arm (star-type) black knob turning mechanism used to lock this lid are physically intact. The white spiral hose and union connections providing the link between the lid and the main body appear sound. The analog pressure gauges (manometers) on the front panel have not sustained physical damage. The red emergency stop button (EMERGENCY) with a yellow collar located at the bottom of the front panel is intact and pressable.

Electronic Components and Display Analysis

The electronic control panel of the device is active, and power is observed to be reaching the device. There is no physical tear or deformation on the membrane keypad. The data on the control panel is listed below:

• Digital Displays: The upper green digital display shows the temperature (t) value, while the lower green digital display shows the time (MINUTE) value. It has been observed that these values (e.g., 126/01, 103/03, 087/05) change during transitions between images.
• Cycle Indicators (Right Column): LED notification lights indicating the PREPARATION, PRE-VACUUM, STERILIZATION, POST-VACUUM, AIR CHARGE, and CYCLE COMPLETED stages are present. In one image, AIR CHARGE is active, while in others, the LED above the START button is observed to be active.
• Warning Indicators (Bottom Left): LID OPEN, OVERPRESSURE, HEATER FAILURE, and LOW WATER LEVEL warning LEDs are present. None of these LEDs are illuminated.
• Control Buttons: TEMP SET, TIME SET, POST-VACUUM SET, START, up/down arrow keys, and an alarm mute/reset button are present.

Accessories and Connections

A thick black power cable emerging from the right rear of the device and a red industrial-type three-phase electrical plug connected to its end are present. The plug is inserted into the wall socket. In the middle part of the control panel, there is a thin printer or data output slot, likely used for obtaining cycle reports. No external accessories such as a sterilization basket are visible inside or around the device.

Label and Warning Information

Warning labels are placed on the top lid of the device to ensure user safety:

• A circular CAUTION! label with black text on a yellow background is located in the center of the lid locking mechanism.
• A rectangular label with a yellow triangular warning sign and the text CAUTION! HOT SURFACE / ATTENTION! HOT SURFACE is located on the front edge of the lid.

Malfunction and Risk Assessment

No broken parts, severed cables, or error codes appearing on the screen (Heater Failure, etc., warning lights are not illuminated) that would hinder the device’s operation have been detected in the images. The dusty environment of the device and the contamination on its surface indicate the necessity for detailed cleaning and calibration before clinical use. No serious potential malfunction risk has been observed.