← Back to catalogue

Cincha Epicondilitis NEOPRAIR OS

EUDAMED

Class I (EU MDR)

Ref NPOS172

by Prim, S.a.

Identity

Trade Name
Cincha Epicondilitis NEOPRAIR OS EUDAMED
Device Name
Ortesis de Codo EUDAMED
Model / Reference
NPOS172 EUDAMED

Identifiers

Primary DI / UDI-DI
08434048105953 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

Cincha Epicondilitis NEOPRAIR OS 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Prim, S.a.
EUDAMED SRN
ES-MF-000004651

Sources (1)

  • EUDAMED dc343014-c0e1-4ff2-b3f8-d0d49d781290 61 fields · synced Jun 19, 2026