Onderbeen Prothesekoker

by Livit Orthopedie B.V.

Ref PB-OBP-KOKERModel OBP Koker

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number8720256363PBOBPKOKERJQ Basic UDI-DI 08720256363057UDI-DI	Date26 Nov 2021Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: OBP Koker, PB-OBP-KOKER

Primary DI / UDI-DI: 08720256363057
Basic UDI-DI: 8720256363PBOBPKOKERJQ
EMDN Code: Y062409 Transtibial prostheses (for amputation under knee)

Device Class: Class I
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: NL-MF-000000548

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No