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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

Neoprene ankle stabilizer LIGAMAX… — Class I MDR

MD Atlas
REHA FUND Sp. z o.o.

EUDAMED last updated this device on Apr 9, 2026

Neoprene ankle stabilizer LIGAMAX ANKLE

59039407O1120D7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: REHA FUND Sp. z o.o.
UDI-DI code: 05903940705880
Reference / catalog number: O-1120/1

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View device family (Basic UDI)

Manufacturer information

Organization name: REHA FUND Sp. z o.o.
SRN: PL-MF-000047481
Manufacturer status: Active

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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

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: Neoprene ankle stabilizer LIGAMAX ANKLE
UDI-DI code: 05903940705880
Basic UDI-DI: 59039407O1120D7
Reference / catalog number: O-1120/1
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: Used as a preventive measure in sport and when returning to physical activity after an injury.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y06120601PASSIVE ANKLE-FOOT ORTHOSES

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

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