gudid Primary ID: LHR-S5-1064

DermRays Revive (UDI LHR-S5-1064)

Manufactured by Wuhan Lotuxs Technology Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DermRays Revive (Model/Catalog Number: LHR-S5-1064) is a medical device manufactured by Wuhan Lotuxs Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification GEX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: LHR-S5-1064
Product Code / EMDN: GEX
Device Name
Database Sync Date: 2026-08-09 09:04:54

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 DermRays Revive?

The registered manufacturer of record for DermRays Revive is Wuhan Lotuxs Technology Co.,Ltd..

What is the Primary UDI-DI identifier for DermRays Revive?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LHR-S5-1064.

What classification code is assigned to this device?

This device is registered under product classification code GEX.

Similar Classification Devices (GEX)

Other Devices by Wuhan Lotuxs Technology Co.,Ltd.

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