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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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KT Motion — 4 UDI-DI variants, MDR

MD Atlas
MEDEL Medizinische Elektronik Handelsgesellschaft mbH

Data from EUDAMED, last updated May 23, 2026

KT Motion

426068413NEUROSTIM001G3

4 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: MEDEL Medizinische Elektronik Handelsgesellschaft mbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426068413NEUROSTIM001G3
Device name: KT Motion
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: MEDEL Medizinische Elektronik Handelsgesellschaft mbH
SRN: DE-MF-000000021
Country: Germany
Email: info@medel-hamburg.de
Phone: +49 40 60 60 460

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6AMJ59KB8R0WB48Q13ZX5Q1

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

GENB-001004260684131018
Z1206270504260684131315
GENB-002004260684131117
GENB-003004260684131216