Secondhand Ivac P2000 Syringe Pump

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: 01.10.2025

IVAC P2000 Syringe Pump Analysis Report

Overview and Device Description

The product shown in the images is a syringe pump used in medical environments to ensure the precise and controlled infusion of liquids or medications to patients. The device features a chamber for placing syringes, a plunger mechanism, and a front panel with a digital display and control buttons.

• Product Type: Syringe Pump (Spritzenpumpe)
• Quantity: The images show 1 syringe pump and 1 mounting clamp attached to the device.
• Area of Use: The device is designed to inject medications and fluids into patients at a specific rate and volume during medical procedures, either intravenously or via other routes. The hospital name on the labels indicates that the product is used in clinical settings.

Brand and Model Information

As a result of a detailed visual inspection, the brand and model of the device have been clearly identified. The brand and model information is written in capital letters on the device’s front panel.

• Brand: IVAC
• Model: P2000

Physical Condition and Deformation Assessment

The overall condition of the device clearly indicates that it has been used. While it gives the impression of being an original product, it bears noticeable aesthetic and physical signs of wear and tear.

• Overall Condition: The overall condition of the device is assessed as used.
• Discoloration: The light-colored plastic casing of the device, especially on the front panel and sides, shows distinct yellowing and fading that has occurred over time or due to environmental factors.
• Scratches and Stains: The device casing has numerous scratches, scuff marks, and stains in various places due to use. Particularly noticeable dark scuff marks are visible below the “START” and “STOP” buttons.
• Screen: No cracks or breaks were observed on the digital screen protector of the device, but small scratches may be present on its surface.

Mechanical and Electronic Components

Upon visual inspection, the mechanical parts of the device appear to have maintained their integrity. No comment can be made regarding the operational status of the electronic components, as the device is powered off.

• Mechanical Parts: The syringe placement and plunger mechanism appears physically intact. The plunger arm, adjustment screw, and syringe holder parts are in place, with no significant breaks or damage. The device’s control buttons are physically complete.
• Electronic Parts: Since the device is powered off, the functionality of the screen or electronic circuits could not be tested. There is no display or error message on the screen.

Accessories and Compatibility

In addition to the device, one mounting accessory is visible in the images. Other accessories that might be required for the device’s operation, such as a power cable, are not present.

• Present Accessories: A clamp with an adjustment screw, mounted underneath the device, is present, allowing it to be secured to medical stands or bed rails.
• Missing Parts: The device’s power cable or any syringes are not visible in the images.
• Compatibility: A yellow label on the device indicates compatibility with B.Braun Perfusor 50ml and Injectomat P 50ml brand/model syringes. This suggests that the device is specifically designed for 50 ml capacity syringes.

Label and Code Information

Various informative and identifying labels are present on the device. However, critical information such as serial number or manufacturing date could not be accessed through these labels.

• Hospital Label: A label issued in the name of “HAFENKRANKENHAUS Hamburg” (Hamburg Port Hospital) is located on the front panel. The “Inventar-nummer” (Inventory Number) and maintenance schedule sections on this label are blank.
• Service Label: A green “akmg” logo label displays the date 1204-2006. This date might indicate a maintenance or calibration date.
• Other Information: No label with a clearly legible serial number, lot number, or REF code for the device is present in the images.

Potential Risk Assessment

Visually, the device does not have any obvious breaks or damage that would prevent its operation. However, its age and signs of use provide an indication of potential risks. The prominent yellowing on the casing indicates that the plastic material’s lifespan is advanced. Although the product’s mechanical components appear to be in place visually, their sensitivity or performance may have diminished due to prolonged use. The most significant potential risks are that the device’s calibration may not be current or that its electronic components may be nearing the end of their service life. For the device to operate safely and accurately, it is recommended that it be inspected, maintained, and calibrated by a professional technical service.