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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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NEXUS / PDMS — 8 UDI-DI variants, MDR (NEXUS / CMC GmbH)

MD Atlas
NEXUS / CMC GmbH

Data from EUDAMED, last updated May 23, 2026

NEXUS / PDMS

426068651300AZ

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: NEXUS / CMC GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426068651300AZ
Device name: NEXUS / PDMS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: NEXUS / CMC GmbH
SRN: DE-MF-000007980
Country: Germany
Email: qm-cmc@nexus-ag.de

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FZTBCNX67G7MD8ZZJ1R1ZN6H

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

2.904260686513027
26.204260686513102
2.1004260686513034
25.304260686513089
2.804260686513010
24.204260686513065
25.404260686513096
2.704260686513003