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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 warming center III DTM — 6 UDI-DI variants, MDR

MD Atlas
Barkey GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Barkey warming center III DTM

4059201warm_cent_IIIEU

6 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: 4059201warm_cent_IIIEU
Device name: Barkey warming center III DTM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 17, 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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H1S1C3BRH7ZKWBVS1AV960NV

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

0001119704059201003378
0001119504059201003354
0001119304059201003330
0001119604059201003361
0001119404059201003347
0001129304059201003644