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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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Typenreihe modulux — 8 UDI-DI variants, MDR (modul technik GmbH)

MD Atlas
modul technik GmbH

Data from EUDAMED, last updated May 23, 2026

Typenreihe modulux

426241958modul8GD

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: modul technik GmbH

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Device characteristics

Active deviceAdministers medicine

Legacy certificates

Certificate number: 44911222228
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: TÜV NORD CERT GmbH (0044)
Validity: Dec 3, 2025 → Dec 2, 2030

Identity & classification

Basic UDI-DI: 426241958modul8GD
Device name: Typenreihe modulux
Device model: Typenreihe modulux
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jun 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: modul technik GmbH
SRN: DE-MF-000014647
Country: Germany
Email: info@modul-technik.de
Phone: + 49 2602 9449 0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JYK74C613TF1KDAH9088N2KJ

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

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