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Pro-Flex® XC Torsion

EUDAMED

Class I (EU MDR)

Ref PXT0127LBRModel BU00051

by Össur Iceland ehf.

Identity

Trade Name
Pro-Flex® XC Torsion EUDAMED
Model / Reference
BU00051 EUDAMED
PXT0127LBR EUDAMED

Identifiers

Primary DI / UDI-DI
05690967800246 EUDAMED
Basic UDI-DI
5690967BU00051NA 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

Pro-Flex® XC Torsion 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 729a8172-3b66-42e5-a117-94c6a1dae963 61 fields · synced Sep 18, 2026