Identity
- Trade Name
- HOLZMUNDSPATEL EUDAMED
- Device Name
- Wooden Tongue Depressor EUDAMED
- Model / Reference
- FN-WTD010101 EUDAMED11700 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06978486830128 EUDAMED
- Basic UDI-DI
- 697391169WTD01TB EUDAMED
- EMDN Code
- V9001 TONGUE DEPRESSORS, SINGLE-USE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Holzmundspatel by Finess Healthcare Group Co., Ltd — 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 | 697391169WTD01TB | Class I | Active |
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Manufacturer
- Manufacturer
- Finess Healthcare Group Co., Ltd
- EUDAMED SRN
- CN-MF-000004124
- Authorised Representative
- Zoustech S.L. ES-AR-000002008
Sources (1)
- EUDAMED 42f14f66-d769-4219-a602-3e87bb5c34e3 61 fields · synced Jul 9, 2026