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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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LUXIMED — 8 UDI-DI variants, MDR (Helmut Hund GmbH)

MD Atlas
Helmut Hund GmbH

Data from EUDAMED, last updated May 23, 2026

LUXIMED

426074436LLK0604U

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: Helmut Hund GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074436LLK0604U
Device name: LUXIMED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 18, 2022

Manufacturer & authorised representative

Manufacturer

Name: Helmut Hund GmbH
SRN: DE-MF-000006335
Country: Germany
Email: j.haus@hund.de
Phone: +49 6441 20040

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01FN6ERGCVA6BB8GZCAR9G7AQ2

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

HT351804260744360006
HT352304260744360013
HT353004260744360020
HT354004260744360037
HT481804260744360044
HT482304260744360051
HT483004260744360068
HT484004260744360075