Identity
- Trade Name
- Remo-Wax korvatipat EUDAMED
- Device Name
- Remo-Wax EUDAMED
- Model / Reference
- 163521 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06432100106278 EUDAMED
- Basic UDI-DI
- 643210REM001UD EUDAMED
- EMDN Code
- Q030499 OTOLOGY DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Finland 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
Remo-Wax korvatipat by Orion Oyj — Class IIa — 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 | 643210REM001UD | Class IIa | Active |
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Manufacturer
- Manufacturer
- Orion Oyj
- EUDAMED SRN
- FI-MF-000001595
Sources (1)
- EUDAMED 768550f1-66b9-4c97-90cf-0227a4a34299 61 fields · synced Jun 19, 2026