Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Sterile and non sterile reusable hand… — 170 UDI-DI variants, MDR

MD Atlas
FKG Dentaire Sàrl

Data from EUDAMED, last updated May 23, 2026

Sterile and non sterile reusable hand tools for root canal preparation during endodontic treatment

7640142410301029G

170 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: FKG Dentaire Sàrl

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 7640142410301029G
Device name: Sterile and non sterile reusable hand tools for root canal preparation during endodontic treatment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 23, 2024

Manufacturer & authorised representative

Manufacturer

Name: FKG Dentaire Sàrl
SRN: CH-MF-000017925
Country: Switzerland
Email: info@fkg.ch
Phone: +41329242244

Authorised representative

Name: Emergo Europe B.V.
SRN: NL-AR-000000116
Country: Netherlands
Phone: +31 70 345 8570

Variants by status

UDI-DI variants

170 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01JAQN93ZB6YBVC52F3B99KBMR

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

01.153.31.020.CG07640142415367
01.153.31.055.CG07640142415435
01.153.21.S45.CG07640142415046
01.153.25.S45.CG07640142415312
01.153.21.045.CG07640142414940
01.153.31.060.CG07640142415442
01.153.31.045.CG07640142415411
01.153.25.015.CG07640142415091
01.153.21.050.CG07640142414964
01.153.31.080.CG07640142415466
01.153.25.070.CG07640142415268
01.153.21.035.CG07640142414902
01.153.21.060.CG07640142414988
01.153.25.030.CG07640142415152
01.153.31.035.CG07640142415398
01.153.25.S15.CG07640142415299
01.153.31.025.CG07640142415374
01.553.31.S15.CG07640142417279
01.553.21.S15.CG07640142417033
01.553.21.030.CG07640142427926
01.553.31.040.CG07640142435884
01.553.25.025.CG07640142417118
01.553.21.040.CG07640142427940
01.553.31.020.CG07640142417248
01.553.21.020.CG07640142416968

1 2 3 4 5