gudid Primary ID: Mobile Monitoring Gateway (MMG)

Ascom (UDI Mobile Monitoring Gateway (MMG))

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ascom (Model/Catalog Number: Mobile Monitoring Gateway (MMG)) is a medical device manufactured by Ascom (Sweden) AB. This product is indexed under FDA Product Code / Category Classification MSX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Mobile Monitoring Gateway (MMG)
Product Code / EMDN: MSX
Device Name
Database Sync Date: 2026-08-09 09:21:51

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 Ascom?

The registered manufacturer of record for Ascom is Ascom (Sweden) AB.

What is the Primary UDI-DI identifier for Ascom?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Mobile Monitoring Gateway (MMG).

What classification code is assigned to this device?

This device is registered under product classification code MSX.

Similar Classification Devices (MSX)

Other Devices by Ascom (Sweden) AB

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