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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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LYMPHATREX SUPPORT KKL1 — 251 UDI-DI variants, MDR

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

LYMPHATREX SUPPORT KKL1

4035459DE1407A3Z

251 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: Thuasne Deutschland GmbH

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UDI-DI variants

251 UDI-DI variants

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Applied filters

basicUdiUlid01KD2TQPSRBJKX18MA8T3GKWEA

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

36053180100931804035459402835
36053280200631904035459407694
36053280203931404035459413183
36053180100231204035459402491
36053180102331304035459402927
36053180102330904035459402880
36053180100931704035459402828
36053280204031504035459380713
36053280204031904035459380751
36053280200631704035459407670
36053280202331004035459380386
36053280203931904035459413237
36053280200231104035459359559
36053180103931304035459413039
36053180100331204035459402637
36053280203031704035459359894
36053180104031904035459403405
36053280203931004035459413145
36053280200931604035459380300
36053280204031404035459380706
36053180100232004035459402576
36053180102331604035459402958
36053280200331104035459359696
36053180103930904035459412995
36053280202831804035459380607

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4035459DE1407A3Z
Device name: LYMPHATREX SUPPORT KKL1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: Thuasne Deutschland GmbH
SRN: DE-MF-000006210
Country: Germany
Email: ra@thuasne.de

Variants by status