Identity
- Device Name
- Root Elevator Bein Left EUDAMED
- Model / Reference
- 3020312 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G15830203120 EUDAMED
- Basic UDI-DI
- ++G1583020312QC EUDAMED
- Direct Marketing DI
- G15830203120 EUDAMED
- EMDN Code
- L150301 DENTAL EXTRACTION TOOTH FORCEPS, REUSABLE 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
Root Elevator Bein Left 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 | ++G1583020312QC | 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 7115ec83-02db-4e05-95d6-de9d87e0b399 61 fields · synced Jun 19, 2026