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K2 Kinetic Foot with Pyramid

EUDAMED

Class I (EU MDR)

Ref NSKF300-23-R-1S3

by Trulife Inc.

Identity

Device Name
K2 Kinetic Foot with Pyramid EUDAMED
Model / Reference
NSKF300-23-R-1S3 EUDAMED

Identifiers

Primary DI / UDI-DI
00645517874432 EUDAMED
Basic UDI-DI
00645517FootK2YR EUDAMED
EMDN Code
Y062409 TRANSTIBIAL PROSTHESES (FOR AMPUTATION UNDER 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

K2 Kinetic Foot with Pyramid by Trulife Inc. — 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
Trulife Inc.
EUDAMED SRN
US-MF-000009657
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED b82dc66e-ad01-419b-8a5f-66f72a162b50 61 fields · synced Jul 8, 2026