gudid Primary ID: 53-131

Bone Funnel Inserter (UDI 53-131)

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 Bone Funnel Inserter (Model/Catalog Number: 53-131) 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: 53-131
Product Code / EMDN: HSZ
Device Name: 6x310mm
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 Bone Funnel Inserter?

The registered manufacturer of record for Bone Funnel Inserter is Hankil Tech Medical Co., Ltd..

What is the Primary UDI-DI identifier for Bone Funnel Inserter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 53-131.

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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