← Back to catalogue

K-Files Flex

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 01.554.25.025.CG

by FKG Dentaire Sàrl

Identity

Trade Name
K-FILES FLEX EUDAMEDFDA UDI
Generic Name
Manual endodontic file/rasp, reusable FDA UDI
Device Name
K-FILES FLEX EUDAMED
Flex. K-Files 554, 25 mm, # 25, handle SMG FDA UDI
Model / Reference
01.554.25.025.CG EUDAMEDFDA UDI
Description
Flex. K-Files 554, 25 mm, # 25, handle SMG FDA UDI

Identifiers

Catalog Number
01.554.25.025.CG FDA UDI
Primary DI / UDI-DI
07640142417545 EUDAMEDFDA UDI
Basic UDI-DI
B-07640142417545 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

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

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 Flex by FKG Dentaire Sàrl — Class I — MDD, 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/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 2d5a5fbe-0758-4762-8aee-54c5e6a8d865 61 fields · synced Jun 20, 2026
  • FDA UDI 21efc027-51e1-4b41-a9f3-c4e1e3366516 34 fields · synced May 30, 2026