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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Gehwagen — 4 UDI-DI variants, MDR

MD Atlas
Thomas Hilfen für Körperbehinderte GmbH & Co. Medico KG

Data from EUDAMED, last updated May 23, 2026

Gehwagen

4034089GehwagenDR

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Thomas Hilfen für Körperbehinderte GmbH & Co. Medico KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4034089GehwagenDR
Device name: Gehwagen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: Thomas Hilfen für Körperbehinderte GmbH & Co. Medico KG
SRN: DE-MF-000006303
Country: Germany
Email: info@thomashilfen.de
Phone: +49 0 4761 886 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01G5648P8K6CMRGKSR6M0WTBRP

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

980001887000004034089049663
980001888000004034089049670
980002045110004034089050041
980002050110004034089050065