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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

3-WHEELED WALKER GENEWA PREMIUM 622 — Class I MDR

MD Atlas
REHA FUND Sp. z o.o.

EUDAMED last updated this device on Apr 9, 2026

3-WHEELED WALKER GENEWA PREMIUM 622

59039407RF622KH

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: 05903940705675
Reference / catalog number: RF-622

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Manufacturer information

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

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: 3-WHEELED WALKER GENEWA PREMIUM 622
UDI-DI code: 05903940705675
Basic UDI-DI: 59039407RF622KH
Reference / catalog number: RF-622
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: The walkers are intended to help people with limited mobility who require support when getting up, standing and walking. The walkers enable independent performance of most daily motor activities. Can be used indoors and outdoors.
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.

Y120606WHEELED WALKER

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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On the market

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