← Back to catalogue

Proprio Foot®

EUDAMED

Class I (EU MDR)

Ref PSXU1430LBRModel BU00048

by Össur Iceland ehf.

Identity

Trade Name
Proprio Foot® EUDAMED
Model / Reference
BU00048 EUDAMED
PSXU1430LBR EUDAMED

Identifiers

Primary DI / UDI-DI
05690967923686 EUDAMED
Basic UDI-DI
5690967BU00048NM EUDAMED
EMDN Code
Y062409 TRANSTIBIAL PROSTHESES (FOR AMPUTATION UNDER 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: Mechanical-resistance external ankle-foot prosthesis

Proprio Foot® by Össur Iceland ehf. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Össur Iceland ehf.
EUDAMED SRN
IS-MF-000000173

Sources (1)

  • EUDAMED b0e91fe9-7ee0-4ac1-b8e2-0da52e51e1f8 61 fields · synced Jul 15, 2026