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

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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

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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

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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

No registered UDI-DI variants for this device family.