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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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Organization name
UDI-DI code
Reference / catalog number

Jørn DK — Class I MDR by JØRN IVERSEN RØDEKRO ApS

MD Atlas
JØRN IVERSEN RØDEKRO ApS

EUDAMED last updated this device on May 13, 2026

Jørn DK

574400183-JLR-series-MSZB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: JØRN IVERSEN RØDEKRO ApS
UDI-DI code: 05744001833001
Reference / catalog number: Jørn DK

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Manufacturer information

Organization name: JØRN IVERSEN RØDEKRO ApS
SRN: DK-MF-000011891
Manufacturer status: Active

Related devices

Jørn EK574400183-JLR-series-MSZBOn the market Line DK574400183-JLR-series-MSZBOn the market Line EK574400183-JLR-series-MSZBOn the market Pelican574400183-Pelican-3GOn the market Pelican Bosch574400183-Pelican-3GOn the market

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Denmark; available across 3 countries total.

Country	On market since	Until
DenmarkPrimary placement		Still on market
Norway		Still on market
Sweden		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05744001833001
Basic UDI-DI: 574400183-JLR-series-MSZB
Reference / catalog number: Jørn DK
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y121806PEDAL TRICYCLES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.