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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 / Scoring — 4 UDI-DI variants, MDR (NEXUS / CMC GmbH)

MD Atlas
NEXUS / CMC GmbH

Data from EUDAMED, last updated May 23, 2026

NEXUS / Scoring

426068651700BM

4 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: 426068651700BM
Device name: NEXUS / Scoring
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: Feb 26, 2024

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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HQJJEWVM46KRDMCRT9YVXRHP

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

24.204260686517018
24.104260686517001
25.404260686517049
26.204260686517056