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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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VS200-IVD — 6 UDI-DI variants, IVDR

MD Atlas
Evident Technology Center Europe GmbH

Data from EUDAMED, last updated May 23, 2026

VS200-IVD

4057981VSIVD77

6 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Evident Technology Center Europe GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 4057981VSIVD77
Device name: VS200-IVD
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Evident Technology Center Europe GmbH
SRN: DE-MF-000047416
Country: Germany
Email: etce.info@evidentscientific.com
Phone: +49251798000

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMG2JSNQ2HVS49G0SVND2JS6

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

E970308804057981030881
E970189404057981018940
E970308704057981030874
E970189304057981018933
E970318804057981031888
E970189504057981018957