Secondhand Nanoom HeartPlus NT-180 AED Defibrillator

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: 10.12.2025

Nanoomtech HeartPlus NT-180 Automated External Defibrillator (AED) Analysis Report

Device Identification, Brand and Model Analysis

The device shown in the visuals is an Automated External Defibrillator (AED/OED), a life-saving medical equipment used in cases of sudden cardiac arrest. Upon detailed examination of the logos on the device, the user manual, and the labels on the box, the following identification information has been definitively determined:

• Manufacturer: Nanoomtech Co., Ltd. (South Korean origin)
• Brand: HeartPlus
• Model: NT-180
• Line: Automated External Defibrillator

It is clearly seen that the “NT-180” option is marked in the model selection area on the box, and the phrase “HeartPlus NT-180” is also present on the device’s labels. The device is recognized by its characteristic red body color and the adult/child mode selection switch located in the lower right corner.

Originality and General Condition

The product is seen with its original packaging belonging to Nanoomtech, a logo-emblazoned carrying case, a branded user manual, and original labels including the serial number. The quality of workmanship, screen prints, and accessory details indicate that the product is 100% original.

Condition Assessment: The device itself (main unit) appears to be in excellent cosmetic condition. No scratches, dents, discoloration, or dirt have been detected on the casing. The keypad and screen section are clean. However, there is shelf wear and edge fraying on the product’s outer cardboard box. Most of the included accessories (cable, pad/battery cartridge) are still in their sealed packaging, which suggests that the product may be unused or merely open-box.

Accessories and Package Contents

The visuals show that the box contents are quite comprehensive and include the essential parts required for an AED kit. The detected parts are as follows:

• 1 Unit HeartPlus NT-180 Defibrillator Main Unit
• 1 Red-colored, Logo-emblazoned Carrying Case
• 1 Nanoomtech HeartPlus NT-180 User Manual
• 1 Cartridge in silver packaging (Likely Battery and Pad Set combined)
• 1 Installation/Introduction CD (Labeled HeartPlus AED, NT-MPR)
• 1 Data Transfer Cable (For computer connection, in sealed packaging)
• 1 Carrying Strap (Black, with metal hooks)
• 1 White-packaged cleaning cloth or extra protective material (Labeled Nanoomtech)

Label Information, Dates, and Technical Data

Critical technical data has been collected from the labels on the device’s box and the sealed silver package. These dates are of vital importance regarding the product’s current status:

Outer Box Label Information:

• Model Name: HeartPlus NT-180 (Marked)
• Serial Number (SN): NT180-S14-00007
• Manufacturing Date: 2014.04.02
• Weight: 1.9kg
• Power Specifications: Non-Rechargeable Lithium-ion Battery, DC 21V-1400mAh / 9V-1400mAh
• Certification: CE 0120

Silver Cartridge Package Label Information:

• Content Description: How to install a new cartridge
• SN (Cartridge): 10010-1010-1600518
• Date: 2018.03.03 (This date is likely a manufacturing or expiration date; however, being later than the device’s main production year may indicate it is a subsequently procured or revised part. Considering the current date, however, this date is old.)

Device Interface and Controls

The front face of the device shown in Visual 3 has the following controls:

• Mode Switch: A rotary switch for toggling between “Adult” and “Infant/Child” options.
• Shock Button: A button with a lightning icon, used to deliver a shock when necessary.
• Info/Microphone Button: A button labeled with an “i”.
• Visual Instructions: Pictorial instructions numbered 1-2-3-4 showing how to attach the electrodes (pads) to the patient are present inside the cover and on the device body.

Battery and Shelf Life Risk

This section of the report is critically important for medical device safety. The manufacturing date on the device’s outer box appears as 2014, and the date on the sealed cartridge packaging appears as 2018. Defibrillator batteries and pads (electrodes) have a specific shelf life (typically 2-5 years). Given that a long time has passed since these dates on the product, there is a very high probability that the current battery and pads have exceeded their service life.

Even if the product is visually in “new” condition, the expiration of the shelf life of its chemical components (lithium battery and gel pads) could cause the device not to function in an emergency or the pads not to adhere. These parts may need to be replaced.

Areas of Use

The Nanoomtech HeartPlus NT-180 is used by individuals trained in first aid and healthcare professionals to restore normal heart rhythm in patients experiencing cardiac arrest by delivering an electric shock. Thanks to its adult and child modes, it caters to a wide patient profile. It is suitable for deployment in areas such as ambulances, hospitals, shopping malls, schools, and workplaces.

Potential Malfunction and Risk Status

No physical breakage, cracks, liquid contact, or corrosion has been detected in the visuals. The mechanical components of the device (cover, buttons, carrying handle) appear sturdy. However, as stated above, there is a risk of historical obsolescence concerning the product’s consumables (battery/cartridge). While testing the electronic functions of the device cannot be done visually, risks such as the internal clock battery running out or capacitors losing their properties may exist if such devices are stored for extended periods. Therefore, it is recommended that the device undergo an authorized service inspection and that the freshness of the consumables be verified “before preparing for medical use”.