gudid Primary ID: MASK LM YELLOW/CE-0500

E-LIGHT LINE (UDI MASK LM YELLOW/CE-0500)

Manufactured by ESPANSIONE MARKETING SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The E-LIGHT LINE (Model/Catalog Number: MASK LM YELLOW/CE-0500) is a medical device manufactured by ESPANSIONE MARKETING SPA. This product is indexed under FDA Product Code / Category Classification GEX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MASK LM YELLOW/CE-0500
Product Code / EMDN: GEX
Device Name
Database Sync Date: 2026-08-09 09:04:29

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 E-LIGHT LINE?

The registered manufacturer of record for E-LIGHT LINE is ESPANSIONE MARKETING SPA.

What is the Primary UDI-DI identifier for E-LIGHT LINE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MASK LM YELLOW/CE-0500.

What classification code is assigned to this device?

This device is registered under product classification code GEX.

Similar Classification Devices (GEX)

Other Devices by ESPANSIONE MARKETING SPA

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