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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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Barbed Broaches — 55 UDI-DI variants, MDR (FKG Dentaire Sàrl)

MD Atlas
FKG Dentaire Sàrl

Data from EUDAMED, last updated May 23, 2026

Barbed Broaches

7640142410301019E

55 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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UDI-DI variants

55 UDI-DI variants

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Applied filters

basicUdiUlid01KFBGP7G32Y2EARDER4CYWQFA

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

03.050.31.025.CT07640142421221
03.050.31.040.CT07640142421252
03.050.31.050.CT07640142421269
03.050.31.030.CT07640142421238
03.050.31.S25.CT07640142421290
03.050.31.035.CT07640142421245
03.050.31.060.CT07640142421276
01.153.21.010.CG07640142414803
01.153.25.008.CG07640142415053
01.153.21.008.CG07640142414513
01.153.25.010.CG07640142415077
01.153.31.008.CG07640142415336
01.153.31.010.CG07640142415343
01.553.25.008.CG07640142417057
01.553.25.010.CG07640142417064
01.553.31.008.CG07640142417217
01.553.31.010.CG07640142417224
01.553.21.008.CG07640142416920
01.553.21.010.CG07640142416937
S1.1B4.00.0AU.FK07640142424161
S1.1B4.00.0AC.FK07640142424239
01.154.25.006.CG07640142415701
S1.1B4.00.SAL.FK07640142412977
S1.1B4.00.SAJ.FK07640142412953
01.154.25.010.CG07640142415725

1 2 3

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7640142410301019E
Device name: Barbed Broaches
Device model: 03.050.31.025.CT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 19, 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