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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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x40 — 2 UDI-DI variants, MDR (NUVIA Instruments GmbH)

MD Atlas
NUVIA Instruments GmbH

Data from EUDAMED, last updated May 23, 2026

x40

426236243DSCLBRTRSD

2 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: NUVIA Instruments GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426236243DSCLBRTRSD
Device name: x40
Device model: NuMED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 1, 2023

Manufacturer & authorised representative

Manufacturer

Name: NUVIA Instruments GmbH
SRN: DE-MF-000006513
Country: Germany
Email: kontakt@nuvia.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GR6HFXPVZ5ZJ8F91Y30KYR3Z

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

1104010004262362430017
1104010104262362430024