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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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MVE — 25 UDI-DI variants, MDR (Schyns GmbH)

MD Atlas
Schyns GmbH

Data from EUDAMED, last updated May 23, 2026

MVE

426236942100AD

25 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: Schyns GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426236942100AD
Device name: MVE
Device model: MVE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: Schyns GmbH
SRN: DE-MF-000014323
Country: Germany
Email: info@schyns.de
Phone: +49260396110

Variants by status

UDI-DI variants

25 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G01MX522YPD0G5J7ASY671MB

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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11704262369421179
11804262369421186
11904262369421193
12504262369421254
11204262369421124
12404262369421247
12204262369421223
12304262369421230
12004262369421209
12104262369421216
11004262369421100
11104262369421117
10104262369421018
10304262369421032
10604262369421063
10404262369421049
10504262369421056
10204262369421025
10904262369421094
10704262369421070
10804262369421087
11504262369421155
11304262369421131
11404262369421148