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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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evolution — 16 UDI-DI variants, MDR (Vincent Systems GmbH)

MD Atlas
Vincent Systems GmbH

Data from EUDAMED, last updated May 23, 2026

evolution

426075088evolutionJV

16 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: Vincent Systems GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426075088evolutionJV
Device name: evolution
Device model: VINCENTevolution
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 25, 2021

Manufacturer & authorised representative

Manufacturer

Name: Vincent Systems GmbH
SRN: DE-MF-000016437
Country: Germany
Email: einkauf@vincentsystems.de

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FN8HCCV9XYVCKQYEX1EMPC0A

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

Ve5-A-B*04260750881731
Ve5-A-BF*04260750881748
Ve5-A-S*04260750881755
Ve5-A-SF*04260750881762
Ve5-T-B*04260750881779
Ve5-T-BF*04260750881786
Ve5-T-S*04260750881793
Ve5-T-SF*04260750881809
Ve4-A-B*04260750880406
Ve4-A-BF* 04260750880413
Ve4-A-S*04260750880420
Ve4-A-SF*04260750880437
Ve4-T-B* 04260750880444
Ve4-T-BF*04260750880451
Ve4-T-S*04260750880468
Ve4-T-SF*04260750880475