eudamed_udi Primary ID: 04260727755829

Moritz Levo Ausgleichskissen (UDI 04260727755829)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Moritz Levo Ausgleichskissen (Model/Catalog Number: 10.654/4247) is a medical device manufactured by Moritz Reha-Hilfen GmbH. This product is indexed under FDA Product Code / Category Classification V08030102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10.654/4247
Product Code / EMDN: V08030102
Device Name: Kissen zur Dekubitusprophylaxe
Database Sync Date: 2026-08-09 16:28:53

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 Moritz Levo Ausgleichskissen?

The registered manufacturer of record for Moritz Levo Ausgleichskissen is Moritz Reha-Hilfen GmbH.

What is the Primary UDI-DI identifier for Moritz Levo Ausgleichskissen?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260727755829.

What classification code is assigned to this device?

This device is registered under product classification code V08030102.

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