gudid Primary ID: 18-018

Remover (UDI 18-018)

Manufactured by Hankil Tech Medical Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Remover (Model/Catalog Number: 18-018) is a medical device manufactured by Hankil Tech Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification HSZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 18-018
Product Code / EMDN: HSZ
Device Name: 2.1/250mm
Database Sync Date: 2026-08-09 09:21:21

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Remover?

The registered manufacturer of record for Remover is Hankil Tech Medical Co., Ltd..

What is the Primary UDI-DI identifier for Remover?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18-018.

What classification code is assigned to this device?

This device is registered under product classification code HSZ.

Similar Classification Devices (HSZ)

Other Devices by Hankil Tech Medical Co., Ltd.

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