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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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Duschstühle — 7 UDI-DI variants, MDR

MD Atlas
REBOTEC Rehabilitationsmittel GmbH

Data from EUDAMED, last updated May 23, 2026

Duschstühle

4046678_STDSSx-0002-130HY

7 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: REBOTEC Rehabilitationsmittel GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4046678_STDSSx-0002-130HY
Device name: —
Device model: Duschstühle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 14, 2024

Manufacturer & authorised representative

Manufacturer

Name: REBOTEC Rehabilitationsmittel GmbH
SRN: DE-MF-000009447
Country: Germany
Email: info@rebotec.de
Phone: +49 5431 9416 0

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HRYFXDPJPSY7VD291J390HZ9

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

363003004046678003802
332542004046678007381
332102004046678012873
332542204046678009811
332542104046678009804
332032004046678013627
332442004046678010251