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.

BIORACE — 293 UDI-DI variants, MDR (FKG Dentaire Sàrl)

MD Atlas
FKG Dentaire Sàrl

Data from EUDAMED, last updated May 23, 2026

BIORACE

7640142410401029T

293 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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: 7640142410401029T
Device name: BIORACE
Device model: 01.7B0.00.0EO.FK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 20, 2026

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

293 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

basicUdiUlid01KFDMS8GE9J5KWQN6NCTBXZH5

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

01.7B0.00.0EZ.FK07640142411406
S1.7B0.00.SCL.FK07640142424338
01.7B0.00.0FG.FK07640142411710
01.7B0.00.0FK.FK07640142412168
01.7B0.00.SAG.FK07640142411208
S1.7B0.00.0DY.FK07640142412984
S1.7B0.00.0EU.FK07640142414681
01.7B0.00.0FD.FK07640142411505
S1.7B0.00.0EL.FK07640142413035
S1.7B0.00.0ER.FK07640142414605
01.7B0.00.0EV.FK07640142412144
01.7B0.00.0FP.FK07640142412212
S1.7B0.00.SAH.FK07640142411147
01.7B0.00.0FH.FK07640142411581
01.7B0.00.0FO.FK07640142412205
01.7B0.00.0EQ.FK07640142412038
S1.7B0.00.0EE.FK07640142424307
01.7B0.00.0EW.FK07640142412083
01.7B0.00.0FL.FK07640142412175
S1.7B0.00.0ES.FK07640142414612
S1.7B0.00.0ED.FK07640142424086
S1.7B0.00.0EY.FK07640142424093
S1.7B0.00.0ET.FK07640142414674
01.7B0.00.0FM.FK07640142412182
S1.7B0.00.0EM.FK07640142413059

1 2 3 4 5