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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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Movu — 3 UDI-DI variants, MDR (Movu Mobility AS)

MD Atlas
Movu Mobility AS

Data from EUDAMED, last updated May 31, 2026

Movu

709006556100101DD

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: Movu Mobility AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 709006556100101DD
Device name: Movu
Device model: Movu Rollator
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Movu Mobility AS
SRN: NO-MF-000050993
Country: Norway
Email: oyvind@gedde.no
Phone: 90128400

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KCRER0YQB80WXJBMYNK8RDNN

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

00007090065560000
00207090065560024
00107090065560017