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REAtouch

EUDAMED

Class I (EU MDR)

Ref REAtouch

by Axinesis

Identity

Trade Name
REAtouch EUDAMED
Device Name
REAtouch EUDAMED
Model / Reference
REAtouch EUDAMED

Identifiers

Primary DI / UDI-DI
05430003042014 EUDAMED
Basic UDI-DI
5430003042REAtouch4L EUDAMED
Direct Marketing DI
05430003042014 EUDAMED
EMDN Code
Y0504,Z12062603 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

REAtouch by Axinesis — 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
Axinesis
EUDAMED SRN
BE-MF-000018870

Sources (1)

  • EUDAMED 4797ffa8-b15a-4562-ada7-8ff4155a6afd 61 fields · synced Jun 18, 2026