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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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Warmhalteschrank FW — 8 UDI-DI variants, MDR

MD Atlas
HUWO - Hydrotherapie GmbH

Data from EUDAMED, last updated May 23, 2026

Warmhalteschrank FW

4262534154600VH

8 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: 4262534154600VH
Device name: Warmhalteschrank FW
Device model: 4600
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

8 UDI-DI variants

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Applied filters

basicUdiUlid01JXB0JKXY6KXMYQ6JSR3K6BE7

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

460004262534150330
460004262534150361
460004262534150378
460004262534150354
460004262534150385
460004262534150347
460004262534150316
460004262534150323