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ReFlex Feile
EUDAMEDClass IIa (EU MDR)
Ref ReFlex.25.50Model ReFlex.25.50 ReFlex Feile 25mm #50
Identity
- Trade Name
- ReFlex Feile EUDAMED
- Device Name
- ReFlex Feile EUDAMED
- Model / Reference
- ReFlex.25.50 ReFlex Feile 25mm #50 EUDAMEDReFlex.25.50 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06942512512043 EUDAMED
- Basic UDI-DI
- B-06942512512043 EUDAMED
- EMDN Code
- Q010507 ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
ReFlex Feile by Shenzhen Denco Medical Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06942512512043 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Shenzhen Denco Medical Co., Ltd.
- EUDAMED SRN
- CN-MF-000014271
- Authorised Representative
- Share info GmbH DE-AR-000005132
Sources (1)
- EUDAMED b5ba41b3-bb1c-48d5-98ff-82d955c925f9 61 fields · synced Jun 17, 2026