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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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Rasmus EK — 6 UDI-DI variants, MDR (JØRN IVERSEN RØDEKRO ApS)

MD Atlas
JØRN IVERSEN RØDEKRO ApS

Data from EUDAMED, last updated May 23, 2026

Rasmus EK

574400183-JLR-series-MSZB

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: JØRN IVERSEN RØDEKRO ApS

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Device characteristics

Active deviceReusable

Identity & classification

Basic UDI-DI: 574400183-JLR-series-MSZB
Device name: Rasmus EK
Device model: Cykel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: JØRN IVERSEN RØDEKRO ApS
SRN: DK-MF-000011891
Country: Denmark
Email: iversen@ji.dk
Phone: +45 74669242

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KRFWVKRPRFB0KGS5QR0W743H

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

Jørn DK05744001833001
Jørn EK05744001833018
Line DK05744001833308
Line EK05744001833315
Rasmus DK05744001833605
Rasmus EK05744001833612