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Octane FX

EUDAMED

Class I (EU MDR)

Ref Octane FX

by Sunrise Medical GmbH

Identity

Trade Name
Octane FX EUDAMED
Device Name
Manual Wheelchair RGK EUDAMED
Model / Reference
Octane FX EUDAMED

Identifiers

Primary DI / UDI-DI
04050063060240 EUDAMED
Basic UDI-DI
4050063mwcrgkS5 EUDAMED
Direct Marketing DI
04050063060240 EUDAMED
EMDN Code
Y122106 REAR SELF-PROPELLED WHEELCHAIRS 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

Octane FX by Sunrise Medical GmbH — 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

EUDAMED SRN
DE-MF-000006320

Sources (1)

  • EUDAMED 286c75f2-f805-4e58-8b25-8271ee430196 61 fields · synced Jun 19, 2026