Identity
- Trade Name
- LUMIFIL + EUDAMED
- Device Name
- LUMIFIL + EUDAMED
- Model / Reference
- 3134949 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D92631349491 EUDAMED
- Basic UDI-DI
- ++D9260058000012793ZG EUDAMED
- EMDN Code
- Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
Yes
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
Category: Dental appliance fabrication material, ceramic
Lumifil + by Nordema GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
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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 | ++D9260058000012793ZG | Class IIa | Active |
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Manufacturer
- Manufacturer
- Nordema GmbH
- EUDAMED SRN
- DE-MF-000008684
Sources (1)
- EUDAMED 0db11842-f79a-4af3-bf78-1782d6825b3c 61 fields · synced Oct 6, 2026