Identity
- Device Name
- Reduction support base EUDAMED
- Model / Reference
- 19886 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +ENOU1988691 EUDAMED
- Basic UDI-DI
- ++ENOU100033LL EUDAMED
- EMDN Code
- L0103 DERMOTOMES AND BLADES, REUSABLE 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
Reduction support base by Nouvag AG — 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 | ++ENOU100033LL | Class I | Active |
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Manufacturer
- Manufacturer
- Nouvag Ag
- EUDAMED SRN
- CH-MF-000018882
- Authorised Representative
- Nouvag Dental- und Medizintechnik GmbH DE-AR-000005643
Sources (1)
- EUDAMED 7e07356a-0eeb-4f8f-b775-d6cfe7ae91d9 61 fields · synced Jun 19, 2026