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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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plasmatherm — 63 UDI-DI variants, MDR (Barkey GmbH & Co. KG)

MD Atlas
Barkey GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

plasmatherm

4059201plasmathermTJ

63 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: 4059201plasmathermTJ
Device name: plasmatherm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 2, 2022

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

63 UDI-DI variants

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Applied filters

basicUdiUlid01FPAX7RWJ4WS9PRHRB53KG88Y

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

No registered UDI-DI variants for this device family.