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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

Arm Protectors — Class I MDR by REHA FUND Sp. z o.o.

MD Atlas
REHA FUND Sp. z o.o.

EUDAMED last updated this device on Apr 29, 2026

Arm Protectors

59039407PPP1922QW

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: 05903940710112
Reference / catalog number: PPP1922

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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: Arm Protectors
UDI-DI code: 05903940710112
Basic UDI-DI: 59039407PPP1922QW
Reference / catalog number: PPP1922
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 product is used to stabilize the arms, shoulders, elbows, and head (in the prone position), while simultaneously allowing safe repositioning and bending of the limbs while maintaining stability. It supports the prevention of bedsores, reduces the risk of facial injuries, and provides easier access to the patient through intubation openings.
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.

Y090612ARM AND ELBOW PROTECTIONS

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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