eudamed_udi Primary ID: 04255942216385

Moritz Sommerschlupfsack Körperform senior schwarz (UDI 04255942216385)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Moritz Sommerschlupfsack Körperform senior schwarz (Model/Catalog Number: 10.112-05) is a medical device manufactured by Moritz Reha-Hilfen GmbH. This product is indexed under FDA Product Code / Category Classification Y122499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10.112-05
Product Code / EMDN: Y122499
Device Name: Schlupfsack
Database Sync Date: 2026-08-09 16:29:13

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 Sommerschlupfsack Körperform senior schwarz?

The registered manufacturer of record for Moritz Sommerschlupfsack Körperform senior schwarz is Moritz Reha-Hilfen GmbH.

What is the Primary UDI-DI identifier for Moritz Sommerschlupfsack Körperform senior schwarz?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04255942216385.

What classification code is assigned to this device?

This device is registered under product classification code Y122499.

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