Identity
- Device Name
- Dento Ject EUDAMED
- Model / Reference
- 3021201 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G15830212010 EUDAMED
- Basic UDI-DI
- ++G1583021201Q9 EUDAMED
- Direct Marketing DI
- G15830212010 EUDAMED
- EMDN Code
- Q010399 SURGICAL DENTAL DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Dento Ject by Lipuma — 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 | ++G1583021201Q9 | Class I | Active |
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Manufacturer
- Manufacturer
- Lipuma
- EUDAMED SRN
- PK-MF-000024322
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (1)
- EUDAMED eb97d098-de54-4c65-aa14-88137f2c3d58 61 fields · synced Jun 19, 2026