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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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Mobilio Changing Bed — 10 UDI-DI variants, MDR (Ropox a/s)

MD Atlas
Ropox a/s

Data from EUDAMED, last updated May 23, 2026

Mobilio Changing Bed

57075810013R4

10 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: Ropox a/s

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 57075810013R4
Device name: Mobilio Changing Bed
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ropox a/s
SRN: DK-MF-000020145
Country: Denmark
Email: info@ropox.dk

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KKH45RJQ5SN2Q2SAE8VXDKZN

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

40-30404-505707581000591
40-30204-505707581001253
40-30406-505707581000607
40-30206-505707581001260
40-30408-505707581000614
40-30208-505707581001277
40-30410-505707581000621
40-30210-505707581001284
40-30411-505707581000638
40-30211-505707581001291