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ELEC®plus Revision - femoral head

EUDAMED

Class III (EU MDR)

Ref 727363

by ARTIQO GmbH

Identity

Trade Name
ELEC®plus Revision - femoral head EUDAMED
Device Name
Kugelkopf ELEC®plus Revision 36 L EUDAMED
Model / Reference
727363 EUDAMED

Identifiers

Primary DI / UDI-DI
04251143406150 EUDAMED
Basic UDI-DI
B-04251143406150 EUDAMED
EMDN Code
P090804050201 CERAMIC FEMORAL HEADS, TOTAL HIP REPLACEMENT EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

ELEC®plus Revision - femoral head by ARTIQO GmbH — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
ARTIQO GmbH
EUDAMED SRN
DE-MF-000007336

Sources (1)

  • EUDAMED 7ae7e575-814f-48a7-8ed1-525588651529 61 fields · synced Jun 18, 2026