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Rev-Feile

EUDAMED

Class IIa (EU MDR)

Ref RF.18.D2Model RF.18.D2 Rev-Feile 18mm D2Ref RF-D1-D3Model RF-D1-D3 Rev-Feile 16/18/22mm D1,D1,D2,D2,D3,D3Ref RF.22.D3Model RF.22.D3 Rev-Feile 22mm D3

by Shenzhen Denco Medical Co., Ltd.

Identity

Trade Name
Rev-Feile EUDAMED
Device Name
Rev-Feile EUDAMED
Model / Reference
RF.18.D2 Rev-Feile 18mm D2 EUDAMED
RF.18.D2 EUDAMED
RF-D1-D3 Rev-Feile 16/18/22mm D1,D1,D2,D2,D3,D3 EUDAMED
RF-D1-D3 EUDAMED
RF.22.D3 Rev-Feile 22mm D3 EUDAMED
RF.22.D3 EUDAMED

Identifiers

Primary DI / UDI-DI
06942512512265 EUDAMED
06942512512241 EUDAMED
06942512512272 EUDAMED
Basic UDI-DI
B-06942512512265 EUDAMED
B-06942512512241 EUDAMED
B-06942512512272 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

Rev-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

Manufacturer
Shenzhen Denco Medical Co., Ltd.
EUDAMED SRN
CN-MF-000014271
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (3)

  • EUDAMED b6514a3e-6047-4c13-9a2c-8a559bbada29 61 fields · synced Jul 10, 2026
  • EUDAMED e56afeeb-4147-4d31-83be-9eff93c40a51 61 fields · synced May 17, 2026
  • EUDAMED 7cd8ccb5-b9fa-431f-9f08-3c3945d545b0 61 fields · synced May 18, 2026