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REAtouch Lite 2

EUDAMED

Class I (EU MDR)

Ref REAtouch Lite 2Ref REAtouch Lite

by Axinesis

Identity

Trade Name
REAtouch Lite 2 EUDAMED
REAtouch Lite EUDAMED
Device Name
REAtouch Lite 2 EUDAMED
REAtouch EUDAMED
Model / Reference
REAtouch Lite 2 EUDAMED
REAtouch Lite EUDAMED

Identifiers

Primary DI / UDI-DI
05430003042045 EUDAMED
05430003042021 EUDAMED
Basic UDI-DI
5430003042REAtouchLite2R7 EUDAMED
5430003042REAtouch4L EUDAMED
Direct Marketing DI
05430003042045 EUDAMED
05430003042021 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 Lite 2 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 (3)

  • EUDAMED d495739d-e0b7-4539-8775-5055e311e569 61 fields · synced Jul 25, 2026
  • EUDAMED 3df94ada-e46d-4cac-8711-7678368a2f0e 61 fields · synced May 18, 2026
  • EUDAMED 363bb836-54a2-460d-8c76-cecb525c2e1c 61 fields · synced Jul 25, 2026