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AK Suspension Sleeve

EUDAMED

Class I (EU MDR)

Ref 3-01-AKSS-L-XXXL

by Regal Prosthesis Limited

Identity

Trade Name
AK Suspension Sleeve EUDAMED
Device Name
Prosthetic Suspension Systems EUDAMED
Model / Reference
3-01-AKSS-L-XXXL EUDAMED

Identifiers

Primary DI / UDI-DI
04895200390909 EUDAMED
Basic UDI-DI
48952003003RP6V 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

Category: Mechanical-resistance external ankle-foot prosthesis

AK Suspension Sleeve by Regal Prosthesis Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical-resistance external ankle-foot prosthesis.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
HK-MF-000028642
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 3c2589a8-65aa-4c0d-a901-521a67782ccc 61 fields · synced Sep 30, 2026