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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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Reha-Buggys — 4 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 23, 2026

Reha-Buggys

4034089Reha-BuggysMD

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: 4034089Reha-BuggysMD
Device name: Reha-Buggys
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

basicUdiUlid01G56B1A9YTP4A4HM00R08FWKM

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

980006808001004034089054834
980006809010004034089107745
980006809000004034089102344
980006806500004034089082202