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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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Mowego — 17 UDI-DI variants, MDR (ATO FORM GmbH)

MD Atlas
ATO FORM GmbH

Data from EUDAMED, last updated May 23, 2026

Mowego

42511106MOVEGOCZ

17 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: ATO FORM GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42511106MOVEGOCZ
Device name: Mowego
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: ATO FORM GmbH
SRN: DE-MF-000008880
Country: Germany
Email: r.friedrich@ato-form.com
Phone: +49 6093 944-266

Variants by status

UDI-DI variants

17 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS599ZQETRW2EB8G3GY2JR6H

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

MGO-C109004251110628400
MGO-A210504251110628363
MGO-A212004251110628370
MGO-A207004251110628349
MGO-A110504251110628318
MGO-J110504251110628455
MGO-J109004251110628448
MGO-C207004251110628417
MGO-C107004251110628394
MGO-A112004251110628325
MGO-C209004251110628424
MGO-A209004251110628356
MGO-A214004251110628387
MGO-A114004251110628332
MGO-A107004251110628295
MGO-A109004251110628301
MGO-J107004251110628431