GUDIDData
gudid Primary ID: FTL-HC-09-230-O

Hemoclip (UDI FTL-HC-09-230-O)

Manufactured by Yangzhou Fartley Medical Instrument Technology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hemoclip - Primary ID FTL-HC-09-230-O

Device Regulatory Overview

The Hemoclip (Model/Catalog Number: FTL-HC-09-230-O) is a medical device manufactured by Yangzhou Fartley Medical Instrument Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification PKL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FTL-HC-09-230-O
Product Code / EMDN
PKL
Device Name
rotating, Repositional Hemostasis Clip, 9mm
Database Sync Date
2026-08-09 09:24:44

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Hemoclip?

The registered manufacturer of record for Hemoclip is Yangzhou Fartley Medical Instrument Technology Co., Ltd.

What is the Primary UDI-DI identifier for Hemoclip?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FTL-HC-09-230-O.

What classification code is assigned to this device?

This device is registered under product classification code PKL.

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