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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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Klasse I Zubehör, nicht-invasive… — 2 UDI-DI variants, MDR

MD Atlas
ARTIQO GmbH

Data from EUDAMED, last updated May 30, 2026

Klasse I Zubehör, nicht-invasive Instrumente des 4-motion® Kniesystems, wiederverwendbar

42511434012003BW

2 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: ARTIQO GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 42511434012003BW
Device name: Klasse I Zubehör, nicht-invasive Instrumente des 4-motion® Kniesystems, wiederverwendbar
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: ARTIQO GmbH
SRN: DE-MF-000007336
Country: Germany
Email: info@artiqo.de
Phone: +49 2591-8931500

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KS7TJGM48G13WQN913W5NFEJ

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

4-motion® Instrument Tray04251143403142
4-motion® Lid for Tray04251143406181