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K2 Sensation®

EUDAMED

Class I (EU MDR)

Ref K2P0226RBRModel BU00049

by Össur Iceland ehf.

Identity

Trade Name
K2 Sensation® EUDAMED
Model / Reference
BU00049 EUDAMED
K2P0226RBR EUDAMED

Identifiers

Primary DI / UDI-DI
05690977380974 EUDAMED
Basic UDI-DI
5690967BU00049NP EUDAMED
EMDN Code
Y062403 FOOT PARTIAL PROSTHESES (INCLUDING TOE PROSTHESES) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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 Sensation® by Össur Iceland ehf. — 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
Össur Iceland ehf.
EUDAMED SRN
IS-MF-000000173

Sources (1)

  • EUDAMED 247910d1-f6a3-4d83-a0b5-e77757091138 61 fields · synced Sep 18, 2026