Identity
- Trade Name
- REAtouch Oboc EUDAMED
- Device Name
- REAtouch Oboc EUDAMED
- Model / Reference
- REAtouch Oboc EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05430003042052 EUDAMED
- Basic UDI-DI
- 5430003042REAtouchObocX3 EUDAMED
- Direct Marketing DI
- 05430003042052 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 Oboc 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 5430003042REAtouchObocX3 | Class I | Active |
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Manufacturer
- Manufacturer
- Axinesis
- EUDAMED SRN
- BE-MF-000018870
Sources (2)
- EUDAMED a538327a-b618-4cc3-b623-960ee2a4792e 61 fields · synced Jun 18, 2026
- EUDAMED 07f51648-70ca-4c44-a086-426fe1990f17 61 fields · synced Jun 18, 2026