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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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Therapieliege Modell X elektrisch — 7 UDI-DI variants, MDR

MD Atlas
HUWO - Hydrotherapie GmbH

Data from EUDAMED, last updated May 23, 2026

Therapieliege Modell X elektrisch

4262534153150UY

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4262534153150UY
Device name: Therapieliege Modell X elektrisch
Device model: 3150
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 29, 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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Applied filters

basicUdiUlid01JYXYXGCK8J8T8SRMSGW8BNXV

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

315004262534150422
315004262534150415
315004262534150491
415004262534150545
415004262534150514
415004262534150521
415004262534150538