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Vgk-Xs

EUDAMED

Class I (EU MDR)

Ref VGK060CModel VGK080

by Orthomobility Ltd.

Identity

Trade Name
VGK-XS EUDAMED
Device Name
VGK-X EUDAMED
Model / Reference
VGK080 EUDAMED
VGK060C EUDAMED

Identifiers

Primary DI / UDI-DI
05060777980122 EUDAMED
Basic UDI-DI
506077798VGK-XHM EUDAMED
EMDN Code
Y062415 TRANSFEMORAL PROSTHESES (FOR AMPUTATION ABOVE KNEE) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Vgk-Xs by Orthomobility Ltd. — 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
Orthomobility Ltd.
EUDAMED SRN
GB-MF-000028506
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 61bec67c-027d-4b8a-84e2-d104e6303c2f 61 fields · synced Jul 8, 2026