eudamed_udi Primary ID: 04260203793352

Mobility Set max | schwarz (UDI 04260203793352)

Manufactured by Novafon Elektromedizinische Geräte GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Mobility Set max | schwarz (Model/Catalog Number: 7112-007) is a medical device manufactured by Novafon Elektromedizinische Geräte GmbH. This product is indexed under FDA Product Code / Category Classification Z120612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 7112-007
Product Code / EMDN: Z120612
Device Name: Mobility Set
Database Sync Date: 2026-08-09 17:24:06

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 Mobility Set max | schwarz?

The registered manufacturer of record for Mobility Set max | schwarz is Novafon Elektromedizinische Geräte GmbH.

What is the Primary UDI-DI identifier for Mobility Set max | schwarz?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260203793352.

What classification code is assigned to this device?

This device is registered under product classification code Z120612.

Similar Classification Devices (Z120612)

Other Devices by Novafon Elektromedizinische Geräte GmbH

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