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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

25-43012-6 — Class I MDR by Ropox a/s

MD Atlas
Ropox a/s

EUDAMED last updated this device on Mar 19, 2026

25-43012-6

57075810016RA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ropox a/s
UDI-DI code: 05707581001017
Reference / catalog number: 25-43012-6

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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.

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: 05707581001017
Basic UDI-DI: 57075810016RA
Reference / catalog number: 25-43012-6
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: 165–185 MU10
60–80 MU29

EMDN nomenclature code(s)

V0805038002NON-RIGID SUPPORTS FOR LIFTS (HARNESSES)

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
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Software identification