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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

25-20524-8 — Class I MDR by Ropox a/s

MD Atlas
Ropox a/s

EUDAMED last updated this device on Mar 19, 2026

25-20524-8

57075810015R8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ropox a/s
UDI-DI code: 05707581000874
Reference / catalog number: 25-20524-8

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Manufacturer information

Organization name: Ropox a/s
SRN: DK-MF-000020145
Manufacturer status: Active

Related devices

40-40152-157075810007R9On the market 40-40140-757075810007R9On the market 40-40153-157075810007R9On the market 40-40120-257075810007R9On the market 40-40150-157075810007R9On the market

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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
If the patient does not have the upper body strength to sit in the sling (with or without holding onto the handles), they have a higher risk of slipping out of the sling. This could lead to a fall.

Market distribution

Primary placement in Denmark; available across 3 countries total.

Country	On market since	Until
DenmarkPrimary placement		Still on market
Germany		Still on market
Spain		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05707581000874
Basic UDI-DI: 57075810015R8
Reference / catalog number: 25-20524-8
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)

V0805030102ELECTRIC MOBILE LIFTS

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