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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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artosy buggy — 3 UDI-DI variants, MDR (METEK Köber & Michalski OHG)

MD Atlas
METEK Köber & Michalski OHG

Data from EUDAMED, last updated May 23, 2026

artosy buggy

426248098artosyMP

3 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: METEK Köber & Michalski OHG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426248098artosyMP
Device name: artosy buggy
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: METEK Köber & Michalski OHG
SRN: DE-MF-000039613
Country: Germany
Email: info@metek-edelstahl.de

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HYFP6WGBF82RG79Y8W3X73GG

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

ergo04262480980029
buggy04262480980012
travel04262480980036