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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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Therapielege Modell XS hydraulisch — 7 UDI-DI variants, MDR

MD Atlas
HUWO - Hydrotherapie GmbH

Data from EUDAMED, last updated May 23, 2026

Therapielege Modell XS hydraulisch

4262534154100UQ

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: HUWO - Hydrotherapie GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4262534154100UQ
Device name: Therapielege Modell XS hydraulisch
Device model: 4100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: HUWO - Hydrotherapie GmbH
SRN: DE-MF-000033644
Country: Germany
Email: huwo-gmbh@t-online.de

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JX9T3HEDQBDM01V7C1WZ9YA0

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

410004262534150293
410004262534150439
410004262534150255
410004262534150675
410004262534150460
410004262534150477
410004262534150484