ELEC®plus Revision - femoral head

by ARTIQO GmbH 12 variants

Ref 727284

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-04251143406082 Basic UDI-DI 04251143406082UDI-DI	Date31 Mar 2022Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Kugelkopf ELEC®plus Revision 28 XL
Model / Reference: 727284

Primary DI / UDI-DI: 04251143406082
Basic UDI-DI: B-04251143406082
EMDN Code: P090804050201 Ceramic femoral heads, total hip replacement

Device Class: Class III
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000007336

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Properties

Sterile
Implantable

Other properties (9)

Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No