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Path Feilen

EUDAMED

Class IIa (EU MDR)

Ref PA.25.16Model PA.25.16 Path Feilen 25mm #016

by Shenzhen Denco Medical Co., Ltd.

Identity

Trade Name
Path Feilen EUDAMED
Device Name
Path Feilen EUDAMED
Model / Reference
PA.25.16 Path Feilen 25mm #016 EUDAMED
PA.25.16 EUDAMED

Identifiers

Primary DI / UDI-DI
06942512512470 EUDAMED
Basic UDI-DI
B-06942512512470 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

Path Feilen 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 9ab4b56c-d194-4be9-a79d-1265162633c4 61 fields · synced Jun 18, 2026