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REAplan

EUDAMED

Class IIa (EU MDR)

Ref REAplan

by Axinesis

Identity

Trade Name
REAplan EUDAMED
Device Name
REAplan EUDAMED
Model / Reference
REAplan EUDAMED

Identifiers

Primary DI / UDI-DI
05430003042007 EUDAMED
Basic UDI-DI
B-05430003042007 EUDAMED
EMDN Code
Y0504,Z120616 EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

REAplan by Axinesis — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Axinesis
EUDAMED SRN
BE-MF-000018870

Sources (1)

  • EUDAMED 30b8ccdf-020e-486e-972c-e48c2ce70046 61 fields · synced Jul 9, 2026