Identity
- Trade Name
- Nordema LC Desensitizer EUDAMED
- Device Name
- Nordema LC Desensitizer EUDAMED
- Model / Reference
- 8850 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D92688501 EUDAMED
- Basic UDI-DI
- ++D9360066000000000X7 EUDAMED
- EMDN Code
- Q019008 DENTINAL DESENSITISERS 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
Nordema LC Desensitizer by Nordema GmbH — 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 | ++D9360066000000000X7 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Nordema GmbH
- EUDAMED SRN
- DE-MF-000008684
Sources (1)
- EUDAMED 8aa5b137-2e6d-4c24-bd33-0a45c85b5d45 61 fields · synced Jun 18, 2026