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Reflex Gold Feile

EUDAMED

Class IIa (EU MDR)

Ref ReGo.25.25Model ReGo.25.25 Reflex Gold Feile 25mm #25

by Shenzhen Denco Medical Co., Ltd.

Identity

Trade Name
Reflex Gold Feile EUDAMED
Device Name
Reflex Gold Feile EUDAMED
Model / Reference
ReGo.25.25 Reflex Gold Feile 25mm #25 EUDAMED
ReGo.25.25 EUDAMED

Identifiers

Primary DI / UDI-DI
06942512512166 EUDAMED
Basic UDI-DI
B-06942512512166 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 Gold 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 6bfbca8e-60c3-4e77-88be-d5001a920ce9 61 fields · synced Jun 17, 2026