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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

OG-MO-AXI -ERG-GRY-UN — Class I MDR by Orthoguard Sp. z o.o.

MD Atlas
Orthoguard Sp. z o.o.

EUDAMED last updated this device on Apr 23, 2026

OG-MO-AXI -ERG-GRY-UN

5905957672OG-MO-AXI-ERG6Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Orthoguard Sp. z o.o.
UDI-DI code: 05905957672278
Reference / catalog number: OG-MO-AXI -ERG-GRY-UN

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View device family (Basic UDI)

Manufacturer information

Organization name: Orthoguard Sp. z o.o.
SRN: PL-MF-000050865
Manufacturer status: Active

Related devices

OG-MO-STP-ROL-UNI-UN5905957672OG-MO-STPSROn the market OG-MO-STP-FIX-UNI-UN5905957672OG-MO-STPSROn the market OG-HY-CAR-CHR-UNI-UN5905957672OG-HY-CARPZOn the market OG-MO-AXI -ERG-BGE-UN5905957672OG-MO-AXI-ERG6ZOn the market OG-MO-AXI -ERG-BLK-UN5905957672OG-MO-AXI-ERG6ZOn the market

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: not provided
UDI-DI code: 05905957672278
Basic UDI-DI: 5905957672OG-MO-AXI-ERG6Z
Reference / catalog number: OG-MO-AXI -ERG-GRY-UN
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.

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.

Y12030601ELBOW CRUTCHES

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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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.