gudid Primary ID: FM-HG0001(2300)B

ClearHemograsper (UDI FM-HG0001(2300)B)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ClearHemograsper (Model/Catalog Number: FM-HG0001(2300)B) is a medical device manufactured by FINEMEDIX CO.,LTD.. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FM-HG0001(2300)B
Product Code / EMDN: KGE
Device Name: 5mm/ 2,300mm/ Dial
Database Sync Date: 2026-08-09 09:51:55

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 ClearHemograsper?

The registered manufacturer of record for ClearHemograsper is FINEMEDIX CO.,LTD..

What is the Primary UDI-DI identifier for ClearHemograsper?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FM-HG0001(2300)B.

What classification code is assigned to this device?

This device is registered under product classification code KGE.

Similar Classification Devices (KGE)

Other Devices by FINEMEDIX CO.,LTD.

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