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Pro-Flex® ST

EUDAMED

Class I (EU MDR)

Ref PST0930RBRModel BU00046

by Össur Iceland ehf.

Identity

Trade Name
Pro-Flex® ST EUDAMED
Model / Reference
BU00046 EUDAMED
PST0930RBR EUDAMED

Identifiers

Primary DI / UDI-DI
05690977249035 EUDAMED
Basic UDI-DI
5690967BU00046NH 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® ST 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 af303aec-5b4c-43e5-9f19-4c9c7c0cc4f7 61 fields · synced Sep 18, 2026