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Armex Roll

EUDAMED

Class I (EU MDR)

Ref 0050503Model SOPORTE CABESTRILLO

by Lidermed S.a.

Identity

Trade Name
ARMEX ROLL EUDAMED
Device Name
ARMEX EUDAMED
Model / Reference
SOPORTE CABESTRILLO EUDAMED
0050503 EUDAMED

Identifiers

Primary DI / UDI-DI
08426716505035 EUDAMED
Basic UDI-DI
18426716ARMEX01MZ EUDAMED
Direct Marketing DI
08426716505035 EUDAMED
EMDN Code
Y210924 ARM SUPPORTS 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

Armex Roll by Lidermed S.a. — 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
Lidermed S.a.
EUDAMED SRN
ES-MF-000004664

Sources (1)

  • EUDAMED 6703f32d-358d-4757-960f-483b793f485a 61 fields · synced Jul 11, 2026