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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 — 212 UDI-DI variants, MDR

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

LYMPHATREX SUPPORT KKL1

4035459DE1409A47

212 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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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4035459DE1409A47
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

UDI-DI variants

212 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KD2TR1069JHX0EQJ8K1VZBV8

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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36055180100953004035459404099
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36055281202851804035459382007
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36055381303950504035459434447
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36055180100950504035459404044
36055281202352004035459381956
36055280200251804035459360906
36055281200253004035459361118
36055381303953004035459434492
36055381300252504035459361293
36055180100251804035459403948
36055180104052004035459404310
36055180100650504035459408004
36055281202351504035459381932
36055180100351804035459404006

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