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Re-Flex Shock™

EUDAMED

Class I (EU MDR)

Ref SSPU1260Model BU00051

by Össur Iceland ehf.

Identity

Trade Name
Re-Flex Shock™ EUDAMED
Model / Reference
BU00051 EUDAMED
SSPU1260 EUDAMED

Identifiers

Primary DI / UDI-DI
05690977368170 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

Re-Flex Shock™ 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 f8c4e18a-8150-4d40-ae3d-64ae9ff07b0a 61 fields · synced Sep 17, 2026