Identity
- Trade Name
- SOLO POSTERIOR EXPLORER EUDAMED
- Device Name
- SOLO POSTERIOR EXPLORER EUDAMED
- Model / Reference
- 1017-29 EUDAMED1017-22 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D1231017290 EUDAMEDD1231017220 EUDAMED
- Basic UDI-DI
- ++D123101729WT EUDAMED++D123101722WD EUDAMED
- EMDN Code
- Q01010199 DENTAL RESTORATION DEVICES - OTHER 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
Category: Dental appliance fabrication material, ceramic
Solo Posterior Explorer by Dental Expert — Class I — 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 | ++D123101729WT | 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 (2)
- EUDAMED 17bdae83-3cca-428b-b771-037c4ad9ecde 61 fields · synced Jul 16, 2026
- EUDAMED a17057e5-43b8-4547-a74d-204095f3ab79 61 fields · synced May 16, 2026