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Alargadera para ortesis femoral (bitutor) 3

EUDAMED

Class I (EU MDR)

Ref D19 3P

by Prim, S.a.

Identity

Trade Name
Alargadera para ortesis femoral (bitutor) 3 EUDAMED
Device Name
Ortesis de Rodilla EUDAMED
Model / Reference
D19 3P EUDAMED

Identifiers

Primary DI / UDI-DI
08426680759243 EUDAMED
Basic UDI-DI
843404825ORTESISRODILLASD EUDAMED
EMDN Code
Y061280 LOWER LIMB ORTHOSES - ACCESSORIES 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

Alargadera para ortesis femoral (bitutor) 3 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 b1b98c02-8166-4622-9278-d30c3f946355 61 fields · synced Jun 18, 2026