Secondhand Biotek ELx800 Microplate Reader

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: 18.08.2025

Bio-Tek ELx800 Microplate Reader Analysis Report

General Assessment and Product Description

The device shown in the visuals is a **Bio-Tek ELx800** model microplate reader. Labels on the device state “For in-vitro DIAGNOSTIC USE”, indicating that the product is intended for reading diagnostic test results (e.g., ELISA tests) in a laboratory environment. Based on the logo, labels, and overall build quality, the product is assessed to be original. The scope of the inspection includes a total of **1** main device and **1** 96-well microplate placed in the device’s reader compartment.

Physical Condition Analysis

The overall condition of the device is assessed as **used**. There is a noticeable yellowing of the casing’s original white or cream color, which appears to have occurred over time. Apart from this discoloration, there are no noticeable large cracks, breaks, or dents on the device’s casing. No tears or significant deformations were observed on the front panel’s keypad and LCD screen surface. The ventilation grilles located on the top and rear parts of the device are physically intact.

Technical and Electronic Details

Visual analyses regarding the device’s electronic components are detailed below.

• Screen: The device has an LCD screen on its front panel. Since the device is not powered on in the visuals, no comment can be made regarding the screen’s functionality.
• Ports and Connections: The device’s rear panel features one **PARALLEL PORT** and one **SERIAL PORT** input. No physical damage or deformation is observed on these ports.
• Accessories: External accessories such as the device’s power cable or data cables are not present in the visuals. Only one microplate is found inside the device.
• Battery: There is no visual evidence of an internal or external battery in the device.

Label Information

The following information can be read on the labels located on the rear of the device:

• CE Label: Indicates that the device has CE certification and compliance with “FOR in-vitro DIAGNOSTIC USE”.
• ETL Label: This is a certification label indicating the product’s compliance with safety standards. This label includes standard information such as “CONFORMS TO UL STD. 3101-1” and “CERTIFIED TO CAN/CSA STD. C22.2 NO. 1010.1”.

Labels showing the device’s serial number, lot number, or manufacturing year are not clearly legible in the visuals.

Potential Risk Assessment

Based on the visual inspection, no broken parts, crushed cables, or clearly visible signs of malfunction that would directly impede the device’s operation were detected. The yellowing of the device’s casing is considered a cosmetic condition related to the product’s age and is not expected to affect its functionality. Overall, the product’s physical condition is well-preserved for its age, and no obvious potential risk of malfunction is observed.