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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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Universal III — 4 UDI-DI variants, MDR (Moeck & Moeck GmbH)

MD Atlas
Moeck & Moeck GmbH

Data from EUDAMED, last updated May 23, 2026

Universal III

426021729WD910ZK

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: Moeck & Moeck GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426021729WD910ZK
Device name: Universal III
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: Moeck & Moeck GmbH
SRN: DE-MF-000007979
Country: Germany
Email: jan.iwersen@moeckundmoeck.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HP44GWYMNGE25BMHYSAQNHHH

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

11WD910MS0104260217290311
11WD910MS0204260217290328
11WD910MS0304260217290335
11WD910MM04260217290120