Identity
- Trade Name
- UNIVERSAL AUGMENTATION EXPLORER EUDAMED
- Device Name
- UNIVERSAL AUGMENTATION EXPLORER EUDAMED
- Model / Reference
- 1033-5 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D123103350 EUDAMED
- Basic UDI-DI
- ++D12310335BS EUDAMED
- EMDN Code
- L031102 EXPLORATION PROBES, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
Universal Augmentation Explorer by Dental Expert — 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 | ++D12310335BS | Class I | Active |
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Manufacturer
- Manufacturer
- Dental Expert
- EUDAMED SRN
- PK-MF-000024595
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (1)
- EUDAMED e281a05f-b85d-4061-a9a4-13e3be4e1af8 61 fields · synced Jul 19, 2026