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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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36055381300652004035459408219
36055381300951804035459382120
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36055281200651504035459408134
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36055281203952504035459434423
36055281202852504035459382021
36055280203953004035459434379
36055180104051504035459404297
36055280200251504035459360890
36055280204052504035459381840
36055281204052504035459382083
36055280203051504035459361019
36055381300252004035459361286
36055381303951804035459434461
36055381303052004035459361408

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