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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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Suitcase ramp — 3 UDI-DI variants, MDR (Mobilex A/S)

MD Atlas
Mobilex A/S

Data from EUDAMED, last updated May 23, 2026

Suitcase ramp

57400014ST-RAMPECZB

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: Mobilex A/S

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 57400014ST-RAMPECZB
Device name: Suitcase ramp
Device model: ST-Ramp
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mobilex A/S
SRN: DK-MF-000021885
Country: Denmark
Email: quality@mobilex.dk
Phone: +4587932220

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2F8Q7SRECKNDG25GGNPYY6

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

ST-15205740001483000
ST-12205740001482997
ST-09105740001482980