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: 29.05.2026
Report code: 1780053626
Mindray iMEC12 Patient Monitor Analysis Report
Device Identification
The device shown in the images is a patient monitor. The device features an integrated carrying handle, a screen, control buttons, a rotary selector knob, and physiological parameter connection sockets on the side panel.
Brand and Model Information
The Mindray brand logo is located on the top left corner of the front panel. In the top right corner, the device model is clearly readable as iMEC12. The device brand has been identified as Mindray and the model as iMEC12.
Authenticity Assessment
The brand logo, model text, keypad design, plastic quality, and the technical label on the rear panel indicate that it is an original Mindray product. The craftsmanship of the outer casing and the placement of the labels are consistent with standard manufacturer quality.
Usage Areas
This device is a multi-parameter patient monitor used for continuous monitoring of patients’ vital signs. It is suitable for use in intensive care units, emergency departments, operating rooms, patient transport processes, and general patient wards. The device performs monitoring of parameters such as electrocardiography, pulse oximetry, non-invasive blood pressure, and body temperature.
Quantity Information
There is a total of 1 Mindray iMEC12 patient monitor in the images. No external cables, sensors, cuffs, or accessories belonging to the device are present in the images.
General Condition and Physical Deformation
The general condition of the device appears to be very good and clean. No fractures, cracks, deep scratches, or dents have been detected on the front panel, screen glass, or keypad. There is no significant physical deformation on the plastic body of the device, other than light dust and very minor signs of use.
Mechanical Component Assessment
The gray carrying handle located on the top of the device is in sturdy condition. The rotary selector knob and physical control buttons on the front panel are in place. No wear or tearing has been observed on the buttons. The screws and plastic joints on the rear panel are intact.
Electronic Component and Socket Analysis
The side panel of the device contains socket inputs used for measuring physiological parameters. These sockets are as follows:
- ECG: Green, multi-pin electrocardiography connection socket
- SpO2: Gray, multi-pin pulse oximeter connection socket
- NIBP: Metal and plastic, non-invasive blood pressure measurement hose connection port
- T1: Yellow, two-pin first temperature sensor connection socket
- T2: Yellow, two-pin second temperature sensor connection socket
No breakage, bending, or physical damage is visible on the internal pins or outer frames of the sockets. The rear panel contains 1 RJ45 ethernet port, 1 equipotential grounding terminal, and 1 AC power input socket.
Battery Status
There is an LED indicator icon on the bottom left of the front panel showing the battery status. On the rear panel, there is a cover for the compartment where the internal battery is housed. The physical condition of the battery, such as whether it is swollen or leaking, cannot be directly observed in the images.
Label Information
There is a label on the rear panel of the device containing technical information from the manufacturer. The label includes the following information:
- Supply Voltage: 100-240V ~ 50/60Hz
- Current Rating: 1.1-0.5A
- Certification: CE mark
Although there are barcodes and a serial number field on the label, the serial number, lot number, or REF code cannot be read clearly due to the image angle and resolution.
Screen Analysis
The device screen is in the off state. Therefore, no text, menu, graphics, or error warnings can be displayed on the screen.
Dimensions and Compatibility
The screen size of the device is 12.1 inches, consistent with the model name. There is no direct text on the device regarding adult, pediatric, or neonatal compatibility. However, this model standardly features parameter sockets compatible with all patient groups.
Manufacturing Year and Documents
No clear date information regarding the manufacturing year of the device can be read from the images. No invoice, warranty certificate, or user manual is present in the images.
Usage Duration and Existing Faults
Since the device is turned off, the operating hours or usage duration information could not be determined. As there is no physical breakage or damage on the device, there is no visually detectable existing fault condition.
Potential Fault Risk
The outer casing, sockets, and keypad of the device are quite clean and well-preserved. No crushing on cables, corrosion on sockets, or serious wear on the body has been observed. Accordingly, it is assessed that the device is in good condition and does not carry a risk of a physically induced fault in the near future.
