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Codera Neopreno NEOPRAIR

EUDAMED

Class I (EU MDR)

Ref NP173 XL

by Prim, S.a.

Identity

Trade Name
Codera Neopreno NEOPRAIR EUDAMED
Device Name
Ortesis de Codo EUDAMED
Model / Reference
NP173 XL EUDAMED

Identifiers

Primary DI / UDI-DI
08434048106004 EUDAMED
Basic UDI-DI
843404825ORTESISCODOSW 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 Neopreno NEOPRAIR by Prim 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
Prim, S.a.
EUDAMED SRN
ES-MF-000004651

Sources (1)

  • EUDAMED 2c688376-e091-421a-a17f-12c3fd400bbf 61 fields · synced Jun 19, 2026