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: 23.12.2025
KLF HK-100II Plus Version Infusion Pump Analysis Report
Device Identification
The device in the visuals is an infusion pump used for medical purposes, which enables the controlled delivery of liquid medications or solutions to the patient. The device has a compact structure suitable for desktop use and can be mounted on an IV pole thanks to the apparatus on its rear.
Brand and Model
As a result of detailed visual analysis, the brand and model of the device have been identified as follows:
- Brand: KLF (The “klf” logo is prominently displayed in capital letters on the front panel.)
- Model: HK-100II (Written next to the “klf” logo on the front panel and on the rear label.)
- Version: Plus version (Indicated in a handwritten font right next to the model name.)
- Manufacturer Information: The phrase “Shenzhen Hawk Optical Electronic Instrument Co., Ltd.” is legible on the rear label. This is the manufacturer of the device, but the product is presented with the KLF brand on the front.
Authenticity
The brand prints on the device, model designations, font structure of the “Plus version” phrase, and the arrangement of technical labels on the rear part comply with industrial standards. The screen interface and keypad layout indicate professional manufacturing. According to visual inspection, the product is an original medical device.
Areas of Use
This device is used in intensive care units, emergency rooms, patient care services, and home care services. It is designed to precisely adjust the amount, duration, and rate (ml/hour) of fluids (medications, nutrients, serum, etc.) to be administered intravenously to the patient.
Quantity Information
The visuals show 1 unit of KLF HK-100II Plus Version infusion pump and a cable (partially visible) that appears to be connected to the device’s power input.
General Condition
The device is in used condition. Although the front panel and screen generally appear clean, there is dust and dirt due to use on the device’s rear casing, hinge details, and screw recesses. The device is in working condition; its screen is active.
Physical Deformation
No cracks or fractures have been observed on the general casing of the device. However, the following points are noteworthy:
- Rear Casing: On the blue-colored rear casing, especially in recessed areas and around the screws, accumulated dirt and dust residues are present.
- Mounting Bracket: Dullness and discoloration (initial oxidation or dirt) are visible on the metal tightening screw and movable metal parts on the rear.
- Labels: There are slight lifts at the corners of the rear label.
Mechanical Components
The front cover latch (gray metallic part), which is the mechanism for clamping and guiding the infusion set, appears solid. The IV pole mounting clamp (clamp) located at the rear is physically present, but the threaded part appears dark, which indicates a lack of lubrication or dirt. The carrying handle (green plastic component) is in solid condition.
Electronic Components
As far as can be visually tested, the electronic functions of the device are active:
- Power Lights: The “Power” icon at the bottom left is lit green. The large warning light on the upper part of the device is lit orange/amber (this usually indicates standby mode or a warning).
- Keypad: There is no fading or tearing on the membrane buttons (START, STOP, CLEAR, etc.) on the front panel.
Screen Analysis
The device’s color LCD screen is in working condition and is bright. The following information is displayed on the screen:
- Battery Status: A “Battery in Use” warning and a 90% charge indicator are present. This indicates that the device is operating on battery power.
- Flow Rate: Set to 0.00 ml/h.
- Sound Icon: An icon indicating the audible alert level is present.
- Total Volume (Σ): Displayed as 0.00 ml.
- Date/Time: The system time is displayed as 08/31 12:04:17.
- Interface Language: The interface and keypad are entirely in Turkish.
Battery Status
The screen clearly displays “Battery in Use” and a green charge bar (90%). This proves that the internal battery is present, holds a charge, and can power the device. However, the charge/discharge duration of the battery cannot be commented on from the visual.
Accessories
A white power cable connected to the device is visible in the image. A screw-type mounting bracket (pole clamp) integrated into the device is located on the rear panel. No infusion set or other consumables are present in the visual.
Label Information
Data obtained from the labels on the rear and top panels are as follows:
- Model: HK-100II
- Power Input: 100-240V, 50/60 Hz.
- Serial/Lot Number: A number similar to “20150908” is legible next to “LOT” on the rear label. This is a strong indication that the manufacturing date is September 2015.
- Service Label: On the upper part, there is a label for “3F GRUP MEDİKAL TİC. LTD. ŞTİ.”, presumed to be an authorized service/dealer, and a contact number (0 216 316 29 69).
Connection Ports
The following connection inputs have been identified on the rear panel:
- Standard 3-pin AC Power Input.
- DC Power Input (Round jack).
- Data/Service port (Multi-pin structure similar to a serial port).
Year of Manufacture
Considering the beginning of the LOT number (20150908) on the rear label, the device has been identified as being manufactured in the year 2015.
Documents
No invoice, user manual, or warranty certificate has been found in the visuals. Since the year of manufacture is 2015, it is certain that the factory warranty has expired.
Current Faults
The screen turned on without issues, and no pixel errors are observed. The “Battery in Use” message indicates that the power unit is operational. There is no visible broken part or “Error” code on the screen.
Potential Fault Risks
The device is approximately 10 years old. The dirt on the rear casing and dust accumulation in the fan grilles suggest that dust might have entered the device, which could lead to heating issues in the long term. Furthermore, metal fatigue/dirt on the rear mounting screw indicates that movable parts may require lubrication or maintenance. From a hygiene perspective, a detailed external cleaning is required.
