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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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2Move — 15 UDI-DI variants, MDR (Etac Immedia A/S)

MD Atlas
Etac Immedia A/S

Data from EUDAMED, last updated May 31, 2026

2Move

57080124001M7

15 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: Etac Immedia A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57080124001M7
Device name: 2Move
Device model: Transfer Horizontal
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Etac Immedia A/S
SRN: DK-MF-000019241
Country: Denmark
Email: etac.immedia@etac.com

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01JTQVN85B2YA68GEQE29H1WZN

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

2Move05708012002702
2Move05708012003235
2Move05708012003242
2Move05708012003211
2Move05708012002726
2Move05708012003204
2Move05708012002696
2Move05708012003198
2Move05708012002719
2Move05708012003228
2Move05708012003259
2Move05708012004508
2Move05708012003150
2Move05708012003143
2Move05708012003136