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K-Files

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 01.154.31.045.CG

by FKG Dentaire Sàrl

Identity

Trade Name
K-FILES EUDAMEDFDA UDI
Generic Name
Manual endodontic file/rasp, reusable FDA UDI
Device Name
Sterile and non sterile reusable hand tools for root canal preparation during endodontic treatment EUDAMED
K-Files 154, 31 mm, # 45, handle SMG FDA UDI
Model / Reference
01.154.31.045.CG EUDAMEDFDA UDI
Description
K-Files 154, 31 mm, # 45, handle SMG FDA UDI

Identifiers

Catalog Number
01.154.31.045.CG FDA UDI
Primary DI / UDI-DI
07640142416005 EUDAMEDFDA UDI
Basic UDI-DI
7640142410301029G EUDAMED
FDA Product Code
EKS FDA UDI
EMDN Code
L159004 ENDODONTIC RASPS AND FILES, REUSABLE EUDAMED
GMDN Term
Manual endodontic file/rasp, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual endodontic file/rasp, reusable

K-Files by FKG Dentaire Sàrl — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FKG Dentaire Sàrl
EUDAMED SRN
CH-MF-000017925
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 08585dda-c3a7-4c42-a803-246a8e02e7f5 61 fields · synced Jul 25, 2026
  • FDA UDI 358f8d4c-58e5-4de6-9d49-0503fd042c08 34 fields · synced May 30, 2026