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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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Barkey S-line — 17 UDI-DI variants, MDR (Barkey GmbH & Co. KG)

MD Atlas
Barkey GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Barkey S-line

4059201S-lineXX

17 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: Barkey GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4059201S-lineXX
Device name: Barkey S-line
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Barkey GmbH & Co. KG
SRN: DE-MF-000005854
Country: Germany
Email: info@barkey.de
Phone: +49 5202 9801 0

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01H5HGWBXW0JQS6ZSKE26AMHNX

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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0001117004059201003118
0001115004059201002913
0001114204059201002838
0001116904059201003101
0001115104059201002920
0001115404059201002951
0001115204059201002937
0001114604059201002876
0001114904059201002906
0001114304059201002845
0001117104059201003125
0001114704059201002883
0001116104059201003026
0001115904059201003002
0001115804059201002999
0001116604059201003071