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S-Feile NiTi
EUDAMEDClass IIa (EU MDR)
Ref SF.21.F2Model SF.21.F2 S-Feile NiTi 21mm F2
Identity
- Trade Name
- S-Feile NiTi EUDAMED
- Device Name
- S-Feile NiTi EUDAMED
- Model / Reference
- SF.21.F2 S-Feile NiTi 21mm F2 EUDAMEDSF.21.F2 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06942512511138 EUDAMED
- Basic UDI-DI
- B-06942512511138 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
S-Feile NiTi 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-06942512511138 | 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 1ab1882d-f2e5-449a-89a7-cd51719297c4 61 fields · synced Jun 19, 2026