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K-Deltas XL

EUDAMED

Class I (EU MDR)

Ref MP.27.03.FN

by KINVENT Biomecanique

Identity

Trade Name
K-Deltas XL EUDAMED
Device Name
KForce Deltas XL EUDAMED
Model / Reference
MP.27.03.FN EUDAMED

Identifiers

Primary DI / UDI-DI
03770033274484 EUDAMED
Basic UDI-DI
B-03770033274484 EUDAMED
EMDN Code
Z12062601 DYNAMOMETRIC PLATFORMS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

K-Deltas XL by Kinvent Biomecanique — Class I — 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

EUDAMED SRN
FR-MF-000031884

Sources (1)

  • EUDAMED 5fcb7738-62a3-4c8f-8b7e-624713860a0a 61 fields · synced Jun 18, 2026