GUDIDData
eudamed_udi Primary ID: 04046678000269

Magic-Soft-Anatom (UDI 04046678000269)

Manufactured by REBOTEC Rehabilitationsmittel GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Magic-Soft-Anatom - Primary ID 04046678000269

Device Regulatory Overview

The Magic-Soft-Anatom (Model/Catalog Number: 10780) is a medical device manufactured by REBOTEC Rehabilitationsmittel GmbH. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10780
Product Code / EMDN
Y12030601
Device Name
Unterarmgehstützen
Database Sync Date
2026-08-09 16:29:48

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 Magic-Soft-Anatom?

The registered manufacturer of record for Magic-Soft-Anatom is REBOTEC Rehabilitationsmittel GmbH.

What is the Primary UDI-DI identifier for Magic-Soft-Anatom?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046678000269.

What classification code is assigned to this device?

This device is registered under product classification code Y12030601.

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