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Dental Root Canal Files

EUDAMED

Class I (EU MDR)

Ref TX5.25Model TK.21.006、TK.25.006、TK.31.006、TK.21.008、TK.25.008、TK.31.008、TK.21.010、TK.25.010、TK.31.010、TK.21.015、TK.25.015、TK.31.015、TK.21.020、TK.25.020、TK.31.020、TK.21.025、TK.25.025、TK.31.025、TK.21.030、TK.25.030、etc

by TiaDent Inc

Identity

Device Name
Dental Root Canal Files EUDAMED
Model / Reference
TK.21.006、TK.25.006、TK.31.006、TK.21.008、TK.25.008、TK.31.008、TK.21.010、TK.25.010、TK.31.010、TK.21.015、TK.25.015、TK.31.015、TK.21.020、TK.25.020、TK.31.020、TK.21.025、TK.25.025、TK.31.025、TK.21.030、TK.25.030、etc EUDAMED
TX5.25 EUDAMED

Identifiers

Primary DI / UDI-DI
00810190261958 EUDAMED
Basic UDI-DI
081019317DRCF44 EUDAMED
EMDN Code
Q010507 ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Dental Root Canal Files by TiaDent Inc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
TiaDent Inc
EUDAMED SRN
US-MF-000049704
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED a725d12e-356c-4a56-b486-9fd07bf35095 61 fields · synced Jun 18, 2026