Identity
- Trade Name
- Molt Dent-Med Supplier EUDAMED
- Device Name
- BONE RONGEUR FORCEP EUDAMED
- Model / Reference
- 381-BRF-45-51 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +G714381BRF45510K EUDAMED
- Basic UDI-DI
- ++G714BONERONGEURFORCEP2X EUDAMED
- Direct Marketing DI
- +G714381BRF45510K EUDAMED
- EMDN Code
- L091302 BONE RONGEURS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
Yes
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
Molt Dent-Med Supplier by Molt Dent Med Supplier — 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 | ++G714BONERONGEURFORCEP2X | Class I | Active |
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Manufacturer
- Manufacturer
- Molt Dent Med Supplier
- EUDAMED SRN
- PK-MF-000050065
- Authorised Representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Sources (1)
- EUDAMED bed6bbb5-dd15-485d-9b78-82aaa97c5cd7 61 fields · synced Jun 18, 2026