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Muleta Artritica

EUDAMED

Class I (EU MDR)

Ref K-12550

by Ortoiberica S.L.

Identity

Trade Name
MULETA ARTRITICA EUDAMED
Device Name
MULETA ARTRITICA EUDAMED
Model / Reference
K-12550 EUDAMED

Identifiers

Primary DI / UDI-DI
08431184125500 EUDAMED
Basic UDI-DI
8431184K125509Y EUDAMED
EMDN Code
Y12030601 ELBOW CRUTCHES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Muleta Artritica by Ortoiberica S.L. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Ortoiberica S.L.
EUDAMED SRN
ES-MF-000025780

Sources (1)

  • EUDAMED e43cded8-2588-44b7-a1e8-1eb573a1217c 61 fields · synced Jul 20, 2026