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Akos

EUDAMED

Class I (EU MDR)

Ref M895535Model BU00003

by Össur Iceland ehf.

Identity

Trade Name
AKOS EUDAMED
Model / Reference
BU00003 EUDAMED
M895535 EUDAMED

Identifiers

Primary DI / UDI-DI
05690977567702 EUDAMED
Basic UDI-DI
5690967BU00003MX EUDAMED
EMDN Code
Y062415 TRANSFEMORAL PROSTHESES (FOR AMPUTATION ABOVE KNEE) 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

Category: Mechatronic external knee prosthesis

Akos by Össur Iceland ehf. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Mechatronic external knee prosthesis.

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 3758ff82-bed1-43c9-8ab8-93cffb0cf263 61 fields · synced Jun 19, 2026