gudid Primary ID: E190

Beacon (UDI E190)

Manufactured by Shenzhen Beacon Display Technology Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Beacon (Model/Catalog Number: E190) is a medical device manufactured by Shenzhen Beacon Display Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification KQM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: E190
Product Code / EMDN: KQM
Device Name: Medical Grade Monitor
Database Sync Date: 2026-08-09 09:05:22

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 Beacon?

The registered manufacturer of record for Beacon is Shenzhen Beacon Display Technology Co., Ltd..

What is the Primary UDI-DI identifier for Beacon?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E190.

What classification code is assigned to this device?

This device is registered under product classification code KQM.

Similar Classification Devices (KQM)

Other Devices by Shenzhen Beacon Display Technology Co., Ltd.

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