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C+ Feile

EUDAMED

Class IIa (EU MDR)

Ref CPLUS.31.010Model CPLUS.31.010 C+ Feile 31mm #10

by Shenzhen Denco Medical Co., Ltd.

Identity

Trade Name
C+ Feile EUDAMED
Device Name
C+ Feile EUDAMED
Model / Reference
CPLUS.31.010 C+ Feile 31mm #10 EUDAMED
CPLUS.31.010 EUDAMED

Identifiers

Primary DI / UDI-DI
06942512514610 EUDAMED
Basic UDI-DI
B-06942512514610 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

C+ 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

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Manufacturer

EUDAMED SRN
CN-MF-000014271
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (1)

  • EUDAMED b9e20904-36ec-431b-8bab-85ad7ebbff64 61 fields · synced Jun 19, 2026