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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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Wechselteilbäder — 6 UDI-DI variants, MDR (Unbescheiden GmbH)

MD Atlas
Unbescheiden GmbH

Data from EUDAMED, last updated May 23, 2026

Wechselteilbäder

42519292PartialBath6J

6 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: Unbescheiden GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42519292PartialBath6J
Device name: Wechselteilbäder
Device model: 0.9-9/ 0.9-8/ 0.9-6/ 2.15-1/ 2.17-1/ 2.19-1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: Unbescheiden GmbH
SRN: DE-MF-000007639
Country: Germany
Email: info@unbescheiden.com
Phone: +49 7221 95340

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JCQZ1ZGB7Y4AF9MPTVVBFA6E

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

Arm contrast bath Hauff04251929221717
Arm contrast bath Kneipp04251929221915
Contrast foot bath04251929209807
Contrast limbs bath/ 4-cell-bath04251929209906
Foot contrast bath04251929221519
Four-cell-bath, still04251929209609