gudid Primary ID: MY MASK-E/M500

MY MASK-E (UDI MY MASK-E/M500)

Manufactured by ESPANSIONE MARKETING SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MY MASK-E (Model/Catalog Number: MY MASK-E/M500) is a medical device manufactured by ESPANSIONE MARKETING SPA. This product is indexed under FDA Product Code / Category Classification IRT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MY MASK-E/M500
Product Code / EMDN: IRT
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 MY MASK-E?

The registered manufacturer of record for MY MASK-E is ESPANSIONE MARKETING SPA.

What is the Primary UDI-DI identifier for MY MASK-E?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MY MASK-E/M500.

What classification code is assigned to this device?

This device is registered under product classification code IRT.

Similar Classification Devices (IRT)

Other Devices by ESPANSIONE MARKETING SPA

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