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Codera Epicondilitis Neopreno

EUDAMED

Class I (EU MDR)

Ref ACN403#1

by Orliman, S.L.U.

Identity

Trade Name
CODERA EPICONDILITIS NEOPRENO EUDAMED
Device Name
Brazalete epicondilitis EUDAMED
Model / Reference
ACN403#1 EUDAMED

Identifiers

Primary DI / UDI-DI
08435491833592 EUDAMED
Basic UDI-DI
84350259ORL20308PX EUDAMED
EMDN Code
Y060615 ELBOW ORTHOSES 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

Codera Epicondilitis Neopreno by Orliman, S.L.U. — 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
Orliman, S.L.U.
EUDAMED SRN
ES-MF-000001598

Sources (1)

  • EUDAMED 56636a25-ad0d-45df-8288-25ce00025132 61 fields · synced Sep 18, 2026