Secondhand Mindray PM-9000 Patient Monitor

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: 04.03.2026

SUPER 1-9000 Patient Monitor Analysis Report

Device Identification and Brand Information

The device shown in the visuals is a patient monitor used to track vital parameters. On the front of the device, in the upper right corner of the screen, the word “Super” is present in a stylized handwritten font. In the upper left bezel, the model number “1-9000 PATIENT MONITOR” is clearly readable. In light of this data, the product has been identified as SUPER 1-9000.

Areas of Use

This device is used in hospital emergency departments, intensive care units, operating rooms, and patient rooms; to instantly monitor patients’ vital functions such as ECG, blood pressure (NIBP), blood oxygen saturation (SpO2), and body temperature. With its current hardware, it is suitable for adult patient monitoring.

Quantity and Accessory Information

According to visual analysis, the products included in the package are as follows:

• 1 unit SUPER 1-9000 Main Unit (Monitor).
• 1 SpO2 extension cable and clip-type probe (Adult type, white color).
• 1 NIBP (Blood Pressure) hose (Black).
• 1 NIBP (Blood Pressure) cuff (Gray color, with velcro strap).
• 1 ECG cable (Trunk cable end is visible, lead cables are partially discernible within the tangled cable pile).
• 1 Power cable (Standard black, grounded plug).

General Status and Physical Condition

The device is in used condition. There is a noticeable yellowing (case discoloration) on its casing, which appears to have developed over time. This indicates that the device’s manufacturing year is old and it has been exposed to ambient light for a long time. However, no deep cracks, breaks, or severe damage compromising its integrity have been detected on the casing.

Mechanical and Screen Examination

The control buttons (Freeze, Silence, NIBP Stop/Start, Menu) and the rotary adjustment knob on the front panel of the device are physically in place. The keypad has a membrane structure, and no excessive wear is observed. The green rotary knob (Encoder) appears to be intact. The screen is in the off position; no large scratch or crack that would obstruct viewing has been detected on its glass surface.

Electronic and Port Analysis

Upon examining the side panel of the device, the condition of the connection ports is as follows:

• ECG Port: Black, 5-pin structure, pins are regular, ready for use.
• SpO2 Port: Coded in blue, socket input is clean.
• NIBP Port: Metal quick-coupling connection end is present, not deformed.
• IBP1 and IBP2 Ports: Socket slots for invasive blood pressure monitoring are present but empty.
• T1 and T2 Ports: Black input jacks for Temperature probes are present.
• CO2 and CO Ports: Although located on the panel label, these sections appear to be empty or closed as hardware (optional feature not added).

Label and Calibration Information

In the upper left corner of the device’s front surface, there is a green technical service/calibration label belonging to the “OPTOMED” company. The information on the label is as follows:

• Report No: 24Y – 34173 (As far as readable).
• Application Date: 07/2024
• Validity: 07/2025

This label certifies that the device underwent a biomedical technical service inspection in July 2024 and holds a valid measurement/calibration conformity until July 2025. This is significant positive data regarding the technical condition of the device.

Potential Failure Risk

No mechanical break or missing part has been observed in the visual analysis. There is no physical risk factor other than the yellowing of the casing. The valid calibration label on the device suggests that its electronic functions were recently tested and are operational. However, as the device was not seen plugged in and operating (screen on), no clear data can be provided regarding the screen pixel status and internal battery performance.