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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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wall diagnostic center — 4 UDI-DI variants, MDR

MD Atlas
Luxamed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

wall diagnostic center

426038196WandstationSC

4 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: Luxamed GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426038196WandstationSC
Device name: wall diagnostic center
Device model: wall diagnostic center
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: Luxamed GmbH & Co. KG
SRN: DE-MF-000006437
Country: Germany
Email: info@luxamed.de
Phone: 07344/9290510

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J9NGWDCA15BRK874BKK9Q1AK

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

wall diagnostic center with otoscope04260381965084
wall diagnostic center with otoscope and ear funnel dispenser04260381965015
wall diagnostic center with otoscope and ophthalmoscope04260381965008
wall diagnostic center with variable module04260381965022