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Baston Ergo Blando Aluminio

EUDAMED

Class I (EU MDR)

Ref K-11500-015

by Ortoiberica S.L.

Identity

Trade Name
BASTON ERGO BLANDO ALUMINIO EUDAMED
Device Name
BASTON ERGO BLANDO ALUMINIO EUDAMED
Model / Reference
K-11500-015 EUDAMED

Identifiers

Primary DI / UDI-DI
08431184115006 EUDAMED
Basic UDI-DI
843118411500015CJ 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

Baston Ergo Blando Aluminio 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 065c7b5b-7393-44b8-b983-67693187adfc 61 fields · synced Jun 18, 2026