gudid Primary ID: RE-HSC6-F

Meicen (UDI RE-HSC6-F)

Manufactured by Guangdong Meicen Medical Equipment Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Meicen (Model/Catalog Number: RE-HSC6-F) is a medical device manufactured by Guangdong Meicen Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification IWE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RE-HSC6-F
Product Code / EMDN: IWE
Device Name: Clear Headrest Type-F HNRT-8213
Database Sync Date: 2026-08-09 09:18:21

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 Meicen?

The registered manufacturer of record for Meicen is Guangdong Meicen Medical Equipment Co., Ltd..

What is the Primary UDI-DI identifier for Meicen?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RE-HSC6-F.

What classification code is assigned to this device?

This device is registered under product classification code IWE.

Similar Classification Devices (IWE)

Other Devices by Guangdong Meicen Medical Equipment Co., Ltd.

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