Huamei (UDI HM-PL300)

Manufactured by Shandong Huamei Technology Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Huamei (Model/Catalog Number: HM-PL300) is a medical device manufactured by Shandong Huamei Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification GFE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HM-PL300
Product Code / EMDN: GFE
Device Name
Database Sync Date: 2026-08-09 09:06:39

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 Huamei?

The registered manufacturer of record for Huamei is Shandong Huamei Technology Co.,Ltd..

What is the Primary UDI-DI identifier for Huamei?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HM-PL300.

What classification code is assigned to this device?

This device is registered under product classification code GFE.

Similar Classification Devices (GFE)

Other Devices by Shandong Huamei Technology Co.,Ltd.

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