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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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Shower-/Changing Bed — 6 UDI-DI variants, MDR (Ropox a/s)

MD Atlas
Ropox a/s

Data from EUDAMED, last updated May 23, 2026

Shower-/Changing Bed

57075810011QY

6 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: 57075810011QY
Device name: Shower-/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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KKGXVBKHMBMGVGTN3HCM1RZ7

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

40-25023-405707581000430
40-25073-205707581000461
40-25026-405707581000447
40-25076-205707581000478
40-25029-405707581000454
40-25079-205707581000485